Imagine ...working for a company that knows that its people are the key to its success in the marketplace. A company in which achieving extraordinary results and having a stimulating work experience are part of the same process. We cultivate and embrace a diverse employee population. We recognize that people with diverse backgrounds, experiences and perspectives fuel our growth and enrich our global culture. We are looking for an individual who enjoys working in a fast-paced, team oriented environment, likes to be challenged, and values the opportunity to make a difference. The Senior Research Scientist is responsible for the coordination and execution of product development efforts for Salty initiatives, including potato chips, nuts, and popcorn recipe development and processing. This includes new products & platforms, line extensions, cost savings, alternate supplier and quality improvements. This position will be located in Charlotte, North Carolina. The Senior Research Scientist position is a hands-on personal contributor position that may manage a technician, respond resourcefully to new demands and challenges throughout the product & commercialization process (including bench, pilot plant, and plant trials to create prototypes for consumer testing, etc.) and implement best practices. The successful candidate must demonstrate strong interpersonal skills and the ability to influence decisions within the cross functional team (Marketing, Operations, Engineering, Manufacturing, QA, Sensory, Culinary, Packaging) and externally with and externally with partners such as vendors. The Senior Research Scientist is expected to possess and demonstrate a solid understanding of food science, the business, operations and the commercialization processes. The approach should include a practical application and modification of existing products / new technologies or the identification and innovative creation of new and unique products which achieve business goals. In addition, the position will include the ability to provide technical specifications and support to assure smooth rollouts of new products and processes during plant startups. This includes the provision of comprehensive process documentation to enable smooth commercialization and training of plant personnel. The Senior Research Scientist must support an environment that fosters innovation and calculated risk taking. Essential responsibilities will include but not be limited to: Leading the identification, assessment and validation of formulations from bench-top through commercialization. This includes managing the financial aspects of product development including ingredient costs for plant trials. Ensuring all proper documentation is done accurately and on schedule and that objectives, budget and timetables are met. Conducting and leading assessment and capability studies, product startups / commercialization and provides on-site support to Plant Operations for new products, productivity and quality programs. Fostering an innovation culture in Campbell Snacks by continually introducing new ideas and product concepts for new products, quality improvements, and productivity. Creating, designing, supervising the development of new experimental protocols / best practices required to validate product concepts and prototypes. Independently directing the activities of outside vendors including ingredients and services. Job Complexity: Ability to interact and communicate effectively with Senior Management as well as Plant Management. Must be a good problem solver; able to identify, interpret and analyze the correct data, and provide detailed direction to development projects. Active knowledge and understanding in areas beyond Product Development including Process and Package Development, QA, Project Engineering and thorough understanding of Marketing needs and financial hurdles. Sustain a high level of competence and professionalism in a dynamic business environment. Easily adapts to changing priorities. We're looking for the following abilities and skills: Bachelor of Science degree with a concentration in Food Science, Food Process Engineering, or Chemical Engineering (Master's degree is preferred). Product Development, preferably someone who has successfully commercialized baked products in the market. 4 - 8+ years of related experience with a consumer-packaged goods background Experience with potato chip unit operations is preferred. Experience in nuts and popcorn is a plus. Excellent analytical skills, strong attention to details, communication and interpersonal skills. Ability to handle and lead multiple projects at any given time in a team environment. Passion for food science, product development and consumers as it relates to innovation for new products, line extensions, and productivity opportunities. Ability to think beyond his or her own (R&D) function to consider the organization holistically. Anticipated travel of up to 40%. CSC1 The Company is committed to providing equal opportunity for employees and applicants in all aspects of the employment relationship, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, veteran status, disability, age, religion or any other classification protected by law. In that regard, U.S. applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.
Mar 30, 2020
Full time
Imagine ...working for a company that knows that its people are the key to its success in the marketplace. A company in which achieving extraordinary results and having a stimulating work experience are part of the same process. We cultivate and embrace a diverse employee population. We recognize that people with diverse backgrounds, experiences and perspectives fuel our growth and enrich our global culture. We are looking for an individual who enjoys working in a fast-paced, team oriented environment, likes to be challenged, and values the opportunity to make a difference. The Senior Research Scientist is responsible for the coordination and execution of product development efforts for Salty initiatives, including potato chips, nuts, and popcorn recipe development and processing. This includes new products & platforms, line extensions, cost savings, alternate supplier and quality improvements. This position will be located in Charlotte, North Carolina. The Senior Research Scientist position is a hands-on personal contributor position that may manage a technician, respond resourcefully to new demands and challenges throughout the product & commercialization process (including bench, pilot plant, and plant trials to create prototypes for consumer testing, etc.) and implement best practices. The successful candidate must demonstrate strong interpersonal skills and the ability to influence decisions within the cross functional team (Marketing, Operations, Engineering, Manufacturing, QA, Sensory, Culinary, Packaging) and externally with and externally with partners such as vendors. The Senior Research Scientist is expected to possess and demonstrate a solid understanding of food science, the business, operations and the commercialization processes. The approach should include a practical application and modification of existing products / new technologies or the identification and innovative creation of new and unique products which achieve business goals. In addition, the position will include the ability to provide technical specifications and support to assure smooth rollouts of new products and processes during plant startups. This includes the provision of comprehensive process documentation to enable smooth commercialization and training of plant personnel. The Senior Research Scientist must support an environment that fosters innovation and calculated risk taking. Essential responsibilities will include but not be limited to: Leading the identification, assessment and validation of formulations from bench-top through commercialization. This includes managing the financial aspects of product development including ingredient costs for plant trials. Ensuring all proper documentation is done accurately and on schedule and that objectives, budget and timetables are met. Conducting and leading assessment and capability studies, product startups / commercialization and provides on-site support to Plant Operations for new products, productivity and quality programs. Fostering an innovation culture in Campbell Snacks by continually introducing new ideas and product concepts for new products, quality improvements, and productivity. Creating, designing, supervising the development of new experimental protocols / best practices required to validate product concepts and prototypes. Independently directing the activities of outside vendors including ingredients and services. Job Complexity: Ability to interact and communicate effectively with Senior Management as well as Plant Management. Must be a good problem solver; able to identify, interpret and analyze the correct data, and provide detailed direction to development projects. Active knowledge and understanding in areas beyond Product Development including Process and Package Development, QA, Project Engineering and thorough understanding of Marketing needs and financial hurdles. Sustain a high level of competence and professionalism in a dynamic business environment. Easily adapts to changing priorities. We're looking for the following abilities and skills: Bachelor of Science degree with a concentration in Food Science, Food Process Engineering, or Chemical Engineering (Master's degree is preferred). Product Development, preferably someone who has successfully commercialized baked products in the market. 4 - 8+ years of related experience with a consumer-packaged goods background Experience with potato chip unit operations is preferred. Experience in nuts and popcorn is a plus. Excellent analytical skills, strong attention to details, communication and interpersonal skills. Ability to handle and lead multiple projects at any given time in a team environment. Passion for food science, product development and consumers as it relates to innovation for new products, line extensions, and productivity opportunities. Ability to think beyond his or her own (R&D) function to consider the organization holistically. Anticipated travel of up to 40%. CSC1 The Company is committed to providing equal opportunity for employees and applicants in all aspects of the employment relationship, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, veteran status, disability, age, religion or any other classification protected by law. In that regard, U.S. applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.
LEAD PHARMACY TECHNICIAN TRIBAL HEALTH DEPARTMENT The successful applicant must possess a high school diploma or GED. Certified by the Pharmacy Technician Certification Board and be licensed in the state of Montana or making meaningful progress towards certification. Must have five or more years of experience working in a community pharmacy. Must possess a valid driver's license. All applicants must submit a Tribal application and copy of academic transcript/training certificate, copy of licensure, proof of enrollment in a federally recognized Tribe if other than CSKT and if claiming veteran's preference, a copy of DD214 must be submitted. The successful applicant, if not already employed by the Tribes must pass a pre-hire drug test and serve a mandatory six (6) months probationary period. Salary is negotiable. To apply, contact Personnel at (406) ###-#### Ext. #1259. Tribal applications are also available online at cskt.org. Closing date will be Thursday, March 26, 2020 at 5:30 p.m. CSKT IS A TRIBAL MEMBER PREFERENCE EMPLOYER Tribal Health Department Associated topics: aseptic technique, dietetic, dietician, healthcare, histotechnologist, microbiology, patient, pharmaceutical, pharmacology, therapeutic
Mar 30, 2020
Full time
LEAD PHARMACY TECHNICIAN TRIBAL HEALTH DEPARTMENT The successful applicant must possess a high school diploma or GED. Certified by the Pharmacy Technician Certification Board and be licensed in the state of Montana or making meaningful progress towards certification. Must have five or more years of experience working in a community pharmacy. Must possess a valid driver's license. All applicants must submit a Tribal application and copy of academic transcript/training certificate, copy of licensure, proof of enrollment in a federally recognized Tribe if other than CSKT and if claiming veteran's preference, a copy of DD214 must be submitted. The successful applicant, if not already employed by the Tribes must pass a pre-hire drug test and serve a mandatory six (6) months probationary period. Salary is negotiable. To apply, contact Personnel at (406) ###-#### Ext. #1259. Tribal applications are also available online at cskt.org. Closing date will be Thursday, March 26, 2020 at 5:30 p.m. CSKT IS A TRIBAL MEMBER PREFERENCE EMPLOYER Tribal Health Department Associated topics: aseptic technique, dietetic, dietician, healthcare, histotechnologist, microbiology, patient, pharmaceutical, pharmacology, therapeutic
Summary of Essential Job Functions Provide statistical support to clinical development plans, strategies, endpoint selection, study design, scientific publications, and regulatory meetings Collaborate with the clinical team in the design, analysis, and reporting of data in clinical trials Responsible for the development of Statistical Analysis Plan and reporting results of statistical analyses, including information in the form of graphs, listings, and tables. Provide statistical interpretation of results and explain statistical methodology to team members. Provide statistical oversight to vendors, contractors, and consultants, and mentor junior staff Represent biostatistics function or biometrics department in cross function teams Provide leadership to Biometrics Functional Teams Help head of biostatistics and biometrics leadership team to build up processes, tools, SOPs, and teams Requirements PhD or Master in Statistics, Biostatistics, or relevant field. Less than 1 year experience for candidates with PhD and 2 years for candidates with a Master degree. Pharmaceutical industry experience is preferred Solution orientated for complex clinical questions and translation of these to statistical hypothesis in study design. Fluency with statistical analysis programing software. Strong problem solving, decision making, project management, and leadership skills. Effective communicator: able to explain methodology and consequences of decisions in lay terms; able to understand requests for complex analyses. Effective team player: willingness to go the extra distance to get results, meet deadlines, etc. Excellent writing and oral communications skills.
Mar 30, 2020
Full time
Summary of Essential Job Functions Provide statistical support to clinical development plans, strategies, endpoint selection, study design, scientific publications, and regulatory meetings Collaborate with the clinical team in the design, analysis, and reporting of data in clinical trials Responsible for the development of Statistical Analysis Plan and reporting results of statistical analyses, including information in the form of graphs, listings, and tables. Provide statistical interpretation of results and explain statistical methodology to team members. Provide statistical oversight to vendors, contractors, and consultants, and mentor junior staff Represent biostatistics function or biometrics department in cross function teams Provide leadership to Biometrics Functional Teams Help head of biostatistics and biometrics leadership team to build up processes, tools, SOPs, and teams Requirements PhD or Master in Statistics, Biostatistics, or relevant field. Less than 1 year experience for candidates with PhD and 2 years for candidates with a Master degree. Pharmaceutical industry experience is preferred Solution orientated for complex clinical questions and translation of these to statistical hypothesis in study design. Fluency with statistical analysis programing software. Strong problem solving, decision making, project management, and leadership skills. Effective communicator: able to explain methodology and consequences of decisions in lay terms; able to understand requests for complex analyses. Effective team player: willingness to go the extra distance to get results, meet deadlines, etc. Excellent writing and oral communications skills.
HematoLogics, Inc. has immediate openings in our CAP and COG certified, waterfront Seattle, WA laboratory for NCA/ASCP-certified cytogenetic technologists. Prior experience with cytogenetic analysis of hematologic malignancies is preferred. Job description: Set-up of lineage-specific cytogenetic cultures for leukemia/lymphoma. Metaphase slide preparation. Chromosome analysis. Reagent QC. Equipment maintenance. The ideal candidate should have a passion for providing high-quality and industry-leading clinical laboratory diagnostic services, patient care, continuous learning and scientific advances, attention to detail as well as possess high-complexity technical and inter-personal skill sets to support an interdisciplinary team-work setting (flow cytometry, molecular diagnostics, FISH on site). HematoLogics, Inc. is a privately owned medical practice with a unique combination of academic pursuit and scientific discovery. We have developed an international reputation in the study of myelodysplasia, minimal disease detection, and integration of multiple technologies to detect and monitor treatment of hematologic diseases. We have established international collaborations and clinical trials to validate our approaches and assure that these innovative techniques and technologies will fit into the routine operation of a service oriented hematopathology referral group. Salary commensurate with experience. Excellent benefit and bonus package. Please submit your resume to: or HematoLogics, Inc. Attn. Barbara Zehentner, Ph.D. HCLD (ABB) 3161 Elliott Ave. Suite 200 Seattle, WA 98121
Mar 30, 2020
Full time
HematoLogics, Inc. has immediate openings in our CAP and COG certified, waterfront Seattle, WA laboratory for NCA/ASCP-certified cytogenetic technologists. Prior experience with cytogenetic analysis of hematologic malignancies is preferred. Job description: Set-up of lineage-specific cytogenetic cultures for leukemia/lymphoma. Metaphase slide preparation. Chromosome analysis. Reagent QC. Equipment maintenance. The ideal candidate should have a passion for providing high-quality and industry-leading clinical laboratory diagnostic services, patient care, continuous learning and scientific advances, attention to detail as well as possess high-complexity technical and inter-personal skill sets to support an interdisciplinary team-work setting (flow cytometry, molecular diagnostics, FISH on site). HematoLogics, Inc. is a privately owned medical practice with a unique combination of academic pursuit and scientific discovery. We have developed an international reputation in the study of myelodysplasia, minimal disease detection, and integration of multiple technologies to detect and monitor treatment of hematologic diseases. We have established international collaborations and clinical trials to validate our approaches and assure that these innovative techniques and technologies will fit into the routine operation of a service oriented hematopathology referral group. Salary commensurate with experience. Excellent benefit and bonus package. Please submit your resume to: or HematoLogics, Inc. Attn. Barbara Zehentner, Ph.D. HCLD (ABB) 3161 Elliott Ave. Suite 200 Seattle, WA 98121
Medicare Insurance Agent - Industry-best comp plan, total work freedom Join the revolutionary ASSURANCE platform, and earn from the industry's best comp plan, selling trusted Medicare plans to inbound, in-market shoppers. Get paid before, during, and after AEP. During AEP, we offer service fee commissions and bonuses, just for helping shoppers. Then after AEP, enjoy the largest January payout you've ever seen. Work as an independent, remote, contract agent. Enjoy the freedom of working when you want, from wherever you want, helping inbound, qualified, in-market shoppers - all free to you. Access our system, and eliminate agency inefficiencies and waste with free training, admin, support, product recommendations, and analytics. It's like Uber for insurance! After AEP, sell MediGap, health, or life, all year-round. Join the ASSURANCE agent network, and take advantage of these benefits: Free live, active, inbound shoppers generated from ASSURANCE-owned and operated sites Access to our proprietary system (includes no dialing, product recommendations, analytics, and constant platform improvement), at no cost to you Well-known and trusted carriers 100s of Guides prospecting for you Accessible underwriters A+ BBB-accredited and proven Requirements to access ASSURANCE platform: AHIP certification 12+ life insurance state licenses One year of phone sales experience High speed Internet connection, reliable computer, and headset with microphone Thorough understanding of HIPAA privacy and security laws, DNC, and insurance regulatory laws History of compliant insurance sales practice Working space and equipment that comply with HIPAA privacy and security standards About ASSURANCE: Everyone is unique. But insurance plans are not. Too often, plans offer blanket coverage, charging customers for coverage they don't need while not offering enough of what they do. ASSURANCE celebrates individual uniqueness with our personalized approach to seeking and purchasing insurance. Our platform serves as the intersection between customer and seller, technology and the human touch. We start by asking customers a few questions to learn about their needs. From there, our ground-breaking, proprietary platform analyzes the thousands of data points that make customers unique. This is how we create custom-tailored plans for each and every kind of customer; plans built precisely for their needs and budget. Our team of engineers, data scientists, marketers, architects, and designers are building systems using advanced science to make humans better. We're eliminating insurance industry waste and simplifying the complex. While our technology helps us personalize coverage, our network of experienced agents is how we deliver the right insurance to our customers. All ASSURANCE Medicare agents are 1099, independent contractors and have maximum control over how, where, and when they do their work. ASSURANCE simply provides the tools to make your business as successful as possible. Join ASSURANCE as we reimagine the role of insurance and enhance the personal and financial health of all consumers.
Mar 30, 2020
Full time
Medicare Insurance Agent - Industry-best comp plan, total work freedom Join the revolutionary ASSURANCE platform, and earn from the industry's best comp plan, selling trusted Medicare plans to inbound, in-market shoppers. Get paid before, during, and after AEP. During AEP, we offer service fee commissions and bonuses, just for helping shoppers. Then after AEP, enjoy the largest January payout you've ever seen. Work as an independent, remote, contract agent. Enjoy the freedom of working when you want, from wherever you want, helping inbound, qualified, in-market shoppers - all free to you. Access our system, and eliminate agency inefficiencies and waste with free training, admin, support, product recommendations, and analytics. It's like Uber for insurance! After AEP, sell MediGap, health, or life, all year-round. Join the ASSURANCE agent network, and take advantage of these benefits: Free live, active, inbound shoppers generated from ASSURANCE-owned and operated sites Access to our proprietary system (includes no dialing, product recommendations, analytics, and constant platform improvement), at no cost to you Well-known and trusted carriers 100s of Guides prospecting for you Accessible underwriters A+ BBB-accredited and proven Requirements to access ASSURANCE platform: AHIP certification 12+ life insurance state licenses One year of phone sales experience High speed Internet connection, reliable computer, and headset with microphone Thorough understanding of HIPAA privacy and security laws, DNC, and insurance regulatory laws History of compliant insurance sales practice Working space and equipment that comply with HIPAA privacy and security standards About ASSURANCE: Everyone is unique. But insurance plans are not. Too often, plans offer blanket coverage, charging customers for coverage they don't need while not offering enough of what they do. ASSURANCE celebrates individual uniqueness with our personalized approach to seeking and purchasing insurance. Our platform serves as the intersection between customer and seller, technology and the human touch. We start by asking customers a few questions to learn about their needs. From there, our ground-breaking, proprietary platform analyzes the thousands of data points that make customers unique. This is how we create custom-tailored plans for each and every kind of customer; plans built precisely for their needs and budget. Our team of engineers, data scientists, marketers, architects, and designers are building systems using advanced science to make humans better. We're eliminating insurance industry waste and simplifying the complex. While our technology helps us personalize coverage, our network of experienced agents is how we deliver the right insurance to our customers. All ASSURANCE Medicare agents are 1099, independent contractors and have maximum control over how, where, and when they do their work. ASSURANCE simply provides the tools to make your business as successful as possible. Join ASSURANCE as we reimagine the role of insurance and enhance the personal and financial health of all consumers.
Job Summary Performs diagnostic medical radiographic and fluoroscopic procedures through interpretation. Minimum Qualifications Education/Training Registered by the American Registry of Radiologic Technology; Associate's degree preferred. Experience No experience required. License/Certification/Registration ARRT (American Registry of Radiologic Technologists) certification. Radiology Technologist license in the State of Maryland. CPR certification. Knowledge, Skills & Abilities Verbal and written communication skills. Basic computer skills preferred. Primary Duties and Responsibilities Acquires ordered images including evaluating these images for technical quality. Sends images to appropriate destinations for interpretation. Contributes to the achievement of established department goals and objectives and adheres to department policies, procedures, quality standards and safety standards. Complies with governmental and accreditation regulations. Maintains orderliness and cleanliness of work areas. Reports any unsafe or potentially unsafe conditions. Maintains X-ray and other equipment in efficient operating order. Performs preventative maintenance on a regularly scheduled basis. Obtains patient history, answers patient questions, and explains procedures. Participates in multidisciplinary quality and service improvement teams. Performs other duties as assigned. Performs radiographic examinations. Prepares as required by the profession and the department, such written documentation as evaluation results, individualized treatment plans, and progress reports. Requests and orders supplies as necessary to keep materials on hand at all times. Transports patients to radiographic room and prepares and maintains room. About MedStar Health MedStar Health is dedicated to providing the highest quality care for people in Maryland and the Washington, D.C., region, while advancing the practice of medicine through education, innovation and research. Our 30,000 associates and 5,400 affiliated physicians work in a variety of settings across our health system, including 10 hospitals and more than 300 community-based locations, the largest visiting nurse association in the region, and highly respected institutes dedicated to research and innovation. As the medical education and clinical partner of Georgetown University for more than 20 years, MedStar is dedicated not only to teaching the next generation of doctors, but also to the continuing education and professional development of our whole team. MedStar Health offers diverse opportunities for career advancement and personal fulfillment. Associated topics: aseptic, dietary, healthcare, immunohematology, industrial hygienist, medical, metabolism, microbiology, physiologist, vaccine
Mar 30, 2020
Full time
Job Summary Performs diagnostic medical radiographic and fluoroscopic procedures through interpretation. Minimum Qualifications Education/Training Registered by the American Registry of Radiologic Technology; Associate's degree preferred. Experience No experience required. License/Certification/Registration ARRT (American Registry of Radiologic Technologists) certification. Radiology Technologist license in the State of Maryland. CPR certification. Knowledge, Skills & Abilities Verbal and written communication skills. Basic computer skills preferred. Primary Duties and Responsibilities Acquires ordered images including evaluating these images for technical quality. Sends images to appropriate destinations for interpretation. Contributes to the achievement of established department goals and objectives and adheres to department policies, procedures, quality standards and safety standards. Complies with governmental and accreditation regulations. Maintains orderliness and cleanliness of work areas. Reports any unsafe or potentially unsafe conditions. Maintains X-ray and other equipment in efficient operating order. Performs preventative maintenance on a regularly scheduled basis. Obtains patient history, answers patient questions, and explains procedures. Participates in multidisciplinary quality and service improvement teams. Performs other duties as assigned. Performs radiographic examinations. Prepares as required by the profession and the department, such written documentation as evaluation results, individualized treatment plans, and progress reports. Requests and orders supplies as necessary to keep materials on hand at all times. Transports patients to radiographic room and prepares and maintains room. About MedStar Health MedStar Health is dedicated to providing the highest quality care for people in Maryland and the Washington, D.C., region, while advancing the practice of medicine through education, innovation and research. Our 30,000 associates and 5,400 affiliated physicians work in a variety of settings across our health system, including 10 hospitals and more than 300 community-based locations, the largest visiting nurse association in the region, and highly respected institutes dedicated to research and innovation. As the medical education and clinical partner of Georgetown University for more than 20 years, MedStar is dedicated not only to teaching the next generation of doctors, but also to the continuing education and professional development of our whole team. MedStar Health offers diverse opportunities for career advancement and personal fulfillment. Associated topics: aseptic, dietary, healthcare, immunohematology, industrial hygienist, medical, metabolism, microbiology, physiologist, vaccine
The Manufacturing Tech Transfer Research Associate is primarily responsible for the support of reagent and control slide manufacturing. ELEMENTS: Education/Experience: BS in a relevant discipline and 2-4 years of experience in a lab setting. Communication Skill : Communication of observations, technical findings, and progress to immediate supervisor/immediate team. Maintains accurate and detailed records of operations. May draft and review SOP's and other technical documents. Interpersonal Skill: Works effectively in a team environment; establishes effective relationships with supervisor and team members. Judgment: Demonstrate a general mastery of research/lab processes with an understanding of experimental design and an understanding of data analysis techniques. Works under general supervision to interpret data and results; may offer input re: next steps in design of experiments Execution: Ability to complete a variety of tasks in the lab; offers input regarding improving processes and outcomes. Pay close and consistent attention to detail. Able to communicate data to internal and external audiences. ESSENTIAL FUNCTIONS: Maintain mammalian cell culture inventory and culture various cancer cell lines and prepare them for general use Qualification of Biorepository slides, including staining, classification and analysis Track inventory consumption rates and provides update to laboratory management as necessary Interacts with Quality Assurance for vendor compliance, material receipt Qualification of antibodies and reagents via functional, qualitative, and quantitative assays Partake all in general laboratory duties Adhere to quality systems and good laboratory practices Maintain safe and clean laboratory environment Contribute in the formation, writing, reviewing, and execution of SOP's Maintain accurate and detailed records in accordance with GLP and CLIA regulations Must understand and demonstrate compliance with all applicable regulatory requirements Responsible for supporting a positive, professional, team-oriented, harassment-free work environment by understanding and complying with the Employee Handbook and Safety Policy/Manual and all Human Resources policies, and by demonstrating the Company's values and being a role model for the Company Brand ADDITIONAL DUTIES: May perform additional duties as assigned or directed by management from time to time. REQUIRED COMPETENCIES: Performance Orientation - Is driven by personal performance; achieves all objectives detailed in scorecards and comfortable with quantifiable assessments. Impact Orientation - Performs to stated objectives and driven to make an impact on company goals and patients' lives. Competitive - Dedicated to a competitive spirit that supports the Epic Sciences' goal to be the premier CTC technology in the industry. Sense of Urgency - Has the speed and agility dedicated to the company's goals and performance. Ability to Handle Pressure and Ambiguity - Comfortable with the pressure to be the best and the ability maintain composure and focus in situations of ambiguity and uncertainty. Confidence - Confident in one's skills and abilities; pursues everything with energy; demonstrates the drive and a need to finish especially in the face of resistance or setbacks. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to sit. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Transition from standing and sitting often. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. General office environment. Daily exposure to PCs and networks. The noise level in the work environment is usually moderate. Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Epic Sciences is an Equal Opportunity Employer and committed to the principle of diversity
Mar 30, 2020
Full time
The Manufacturing Tech Transfer Research Associate is primarily responsible for the support of reagent and control slide manufacturing. ELEMENTS: Education/Experience: BS in a relevant discipline and 2-4 years of experience in a lab setting. Communication Skill : Communication of observations, technical findings, and progress to immediate supervisor/immediate team. Maintains accurate and detailed records of operations. May draft and review SOP's and other technical documents. Interpersonal Skill: Works effectively in a team environment; establishes effective relationships with supervisor and team members. Judgment: Demonstrate a general mastery of research/lab processes with an understanding of experimental design and an understanding of data analysis techniques. Works under general supervision to interpret data and results; may offer input re: next steps in design of experiments Execution: Ability to complete a variety of tasks in the lab; offers input regarding improving processes and outcomes. Pay close and consistent attention to detail. Able to communicate data to internal and external audiences. ESSENTIAL FUNCTIONS: Maintain mammalian cell culture inventory and culture various cancer cell lines and prepare them for general use Qualification of Biorepository slides, including staining, classification and analysis Track inventory consumption rates and provides update to laboratory management as necessary Interacts with Quality Assurance for vendor compliance, material receipt Qualification of antibodies and reagents via functional, qualitative, and quantitative assays Partake all in general laboratory duties Adhere to quality systems and good laboratory practices Maintain safe and clean laboratory environment Contribute in the formation, writing, reviewing, and execution of SOP's Maintain accurate and detailed records in accordance with GLP and CLIA regulations Must understand and demonstrate compliance with all applicable regulatory requirements Responsible for supporting a positive, professional, team-oriented, harassment-free work environment by understanding and complying with the Employee Handbook and Safety Policy/Manual and all Human Resources policies, and by demonstrating the Company's values and being a role model for the Company Brand ADDITIONAL DUTIES: May perform additional duties as assigned or directed by management from time to time. REQUIRED COMPETENCIES: Performance Orientation - Is driven by personal performance; achieves all objectives detailed in scorecards and comfortable with quantifiable assessments. Impact Orientation - Performs to stated objectives and driven to make an impact on company goals and patients' lives. Competitive - Dedicated to a competitive spirit that supports the Epic Sciences' goal to be the premier CTC technology in the industry. Sense of Urgency - Has the speed and agility dedicated to the company's goals and performance. Ability to Handle Pressure and Ambiguity - Comfortable with the pressure to be the best and the ability maintain composure and focus in situations of ambiguity and uncertainty. Confidence - Confident in one's skills and abilities; pursues everything with energy; demonstrates the drive and a need to finish especially in the face of resistance or setbacks. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to sit. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Transition from standing and sitting often. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. General office environment. Daily exposure to PCs and networks. The noise level in the work environment is usually moderate. Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Epic Sciences is an Equal Opportunity Employer and committed to the principle of diversity
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that I agree with Takeda's Privacy Notice , Privacy Policy and Terms of Use . Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Manager/ Senior Manager, Analytics and Data Science in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Here, you will be a vital contributor to our inspiring, bold mission. OBJECTIVES: Manager/ Senior Manager, Analytics and Data Science will partner with teams, both within finance and other R&D functions as a critical contributor to the development of new strategic initiatives to derive actionable insights from our data. POSITION OBJECTIVES: Support the R&D Finance organization by understanding reporting and analytic requirements, recommending process improvements, developing data collection, reporting, and publishing systems, and transition maintainable operations to respective teams. Collaborate extensively with the broader R&D organization through subject matter expertise on R&D financial information. Participate in cross functional teams to integration finance data with other internal and externally sourced information to visualize and reporting actionable insights. Will liaise with Data Sciences Institute, Center of Operations Performance, and Information Technology to develop long-term information management strategy, including vision, approach, plans and timeline. Responsible to lead change initiatives in data analytics areas when required. Participate in special projects, as requested. Assist in the development of policies and procedures as they relate to data governance. This position will play a key role in maximizing the value of information throughout R&D. POSITION ACCOUNTABILITIES: Lead change to data analysis and reporting processes for R&D finance and other data science initiatives across R&D functions. Build tools/dashboards to automate reporting and generate insights that will allow managers to quickly and accurately see how our programs and processes are performing. Ensure data integrity of the supported financial reports and dashboards. Ensures required audit documentation and validation reports for applications are maintained. Documents exceptions and communicates issues to management Champion data governance initiative for R&D through representation on internal initiatives including master data, data lake and other projects. Work closely with R&D Finance, portfolio analytics, and IT teams to identify areas of opportunity to leverage technology to drive efficiencies and standardization that will reduce cycle time, and increase productivity across the entire organization. Studies manual financial processes and procedures and makes recommendations on how to automate. Develop and tests new or modified report formats, customized programs to manipulate data; creates or updates functional specifications for new or modified reports and applications. Develop and drive adherence to department standards that ensure that information is reported in a format that is consistent, accurate and meets the needs of the users. Design and maintain end user production reporting. Assist end users with report and query development and maintenance in supported applications. Distributes reports to business line users, as applicable. Create ad-hoc reporting and analysis, as requested. Develops documentation and training for end users on how to effectively use financial management reporting applications. Evaluate and make recommendations of related to data management and analysis Manages technical development activities using project management methodologies. EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS: Encourages new ideas and innovative approaches to continually improve processes. Bachelor's degree required; major in quantitative field, including, Data Science, Accounting, Finance, or a related field preferred 2- 5+ years Data Science/Business Intelligence/Data Analytics, or advanced degree in as quantitative field 2+ years using Python (Pandas, NumPy, scikit-learn), SAS, Stata, or R Minimum 7 years of related business experience required; previous experience working in pharmaceutical or healthcare preferred. The ability to review financial processes and internal controls and make recommendations to improve processes whether through the financial systems or change in operations. The ability to communicate with others in a clear, understandable, and professional manner on the phone or in person, and the demonstrated use of good written and verbal communication skills. The ability to anticipate customer needs. The ability to organize and focus people on key priorities in order to complete several tasks simultaneously with a high degree of accuracy and attention to detail. The ability to build a collaborative network of relationships with people in a variety of functions and roles, and leverage formal and informal networks to accomplish goals. Prior experience with visualization, programming, and data management techniques and tools is required. Business Intelligence, analytics, reporting and visualization technical expertise is required. Database management understanding and reporting experience required. Computer software proficiency to include Microsoft Office applications and financial type systems. TRAVEL REQUIREMENTS: 10% travel, primarily international. WHAT TAKEDA CAN OFFER YOU: 401(k) with company match and Annual Retirement Contribution Plan Tuition reimbursement Company match of charitable contributions Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs Empowering Our People to Shine Discover more at takedajobs.com No Phone Calls or Recruiters Please. Locations Boston, MA Lexington, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time
Mar 30, 2020
Full time
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that I agree with Takeda's Privacy Notice , Privacy Policy and Terms of Use . Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Manager/ Senior Manager, Analytics and Data Science in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Here, you will be a vital contributor to our inspiring, bold mission. OBJECTIVES: Manager/ Senior Manager, Analytics and Data Science will partner with teams, both within finance and other R&D functions as a critical contributor to the development of new strategic initiatives to derive actionable insights from our data. POSITION OBJECTIVES: Support the R&D Finance organization by understanding reporting and analytic requirements, recommending process improvements, developing data collection, reporting, and publishing systems, and transition maintainable operations to respective teams. Collaborate extensively with the broader R&D organization through subject matter expertise on R&D financial information. Participate in cross functional teams to integration finance data with other internal and externally sourced information to visualize and reporting actionable insights. Will liaise with Data Sciences Institute, Center of Operations Performance, and Information Technology to develop long-term information management strategy, including vision, approach, plans and timeline. Responsible to lead change initiatives in data analytics areas when required. Participate in special projects, as requested. Assist in the development of policies and procedures as they relate to data governance. This position will play a key role in maximizing the value of information throughout R&D. POSITION ACCOUNTABILITIES: Lead change to data analysis and reporting processes for R&D finance and other data science initiatives across R&D functions. Build tools/dashboards to automate reporting and generate insights that will allow managers to quickly and accurately see how our programs and processes are performing. Ensure data integrity of the supported financial reports and dashboards. Ensures required audit documentation and validation reports for applications are maintained. Documents exceptions and communicates issues to management Champion data governance initiative for R&D through representation on internal initiatives including master data, data lake and other projects. Work closely with R&D Finance, portfolio analytics, and IT teams to identify areas of opportunity to leverage technology to drive efficiencies and standardization that will reduce cycle time, and increase productivity across the entire organization. Studies manual financial processes and procedures and makes recommendations on how to automate. Develop and tests new or modified report formats, customized programs to manipulate data; creates or updates functional specifications for new or modified reports and applications. Develop and drive adherence to department standards that ensure that information is reported in a format that is consistent, accurate and meets the needs of the users. Design and maintain end user production reporting. Assist end users with report and query development and maintenance in supported applications. Distributes reports to business line users, as applicable. Create ad-hoc reporting and analysis, as requested. Develops documentation and training for end users on how to effectively use financial management reporting applications. Evaluate and make recommendations of related to data management and analysis Manages technical development activities using project management methodologies. EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS: Encourages new ideas and innovative approaches to continually improve processes. Bachelor's degree required; major in quantitative field, including, Data Science, Accounting, Finance, or a related field preferred 2- 5+ years Data Science/Business Intelligence/Data Analytics, or advanced degree in as quantitative field 2+ years using Python (Pandas, NumPy, scikit-learn), SAS, Stata, or R Minimum 7 years of related business experience required; previous experience working in pharmaceutical or healthcare preferred. The ability to review financial processes and internal controls and make recommendations to improve processes whether through the financial systems or change in operations. The ability to communicate with others in a clear, understandable, and professional manner on the phone or in person, and the demonstrated use of good written and verbal communication skills. The ability to anticipate customer needs. The ability to organize and focus people on key priorities in order to complete several tasks simultaneously with a high degree of accuracy and attention to detail. The ability to build a collaborative network of relationships with people in a variety of functions and roles, and leverage formal and informal networks to accomplish goals. Prior experience with visualization, programming, and data management techniques and tools is required. Business Intelligence, analytics, reporting and visualization technical expertise is required. Database management understanding and reporting experience required. Computer software proficiency to include Microsoft Office applications and financial type systems. TRAVEL REQUIREMENTS: 10% travel, primarily international. WHAT TAKEDA CAN OFFER YOU: 401(k) with company match and Annual Retirement Contribution Plan Tuition reimbursement Company match of charitable contributions Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs Empowering Our People to Shine Discover more at takedajobs.com No Phone Calls or Recruiters Please. Locations Boston, MA Lexington, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time
Quality Control Lab Analyst Location Salt Lake City Department Quality & Regulatory Affairs Apply Now USANA Health Sciences is seeking a dedicated and reliable individual to join the quality control laboratoryas a laboratory associate. In this position, you will perform chemical, physical and/or microbiological assays of raw materials and products to ensure they meet the quality standards established by the company. In this entry-level position, you will perform routine quality testing of products. This may include chemical identification testing, pH, particle size analysis, titrations, and HPLC analysis. Your ability to organize work assignments to complete testing in a timely manner will be integral to your success. As you develop in this position, you will participate in a leading laboratory in the industry. Our team works hard at creating a fun work environment and the experience gained in the quality control laboratory can open up doors to move into other positions both in the laboratory as well as in other areas of the company. A successful individual in this position will exemplify USANA's core values and must be self-motivated to produce quality work they can be proud of. Additional Essential Functions Conduct routine experiments and/or analyses Ability to follow written lab procedures Document results of experiments and analyses in notebooks and electronic spreadsheets Operate and maintain lab equipment Understand and adhere to GMP policies and procedures Perform other duties as assigned or needed Qualifications/Knowledge, Skills, and Abilities Requirements Associate's degree in science related field or 2- 5 years professional laboratory experience; Bachelor's degree preferred Must exhibit proficiency in basic laboratory skills and safety practices Ability to perform basic math functions Ability to efficiently and effectively perform all essential position duties and responsibilities with or without reasonable accommodation We've been around a while. We've done some amazing things. We've climbed to the top of the nutritional supplement industry, touching millions of lives along the way. Founded in 1992 by Dr. Myron Wentz, USANA Health Sciences is a U.S.-based international company that manufactures high-quality supplements, personal care, and energy products in our FDA-registered facility in Salt Lake City, Utah. USANA is committed to making the highest quality products without compromise. That's why we use only the purest ingredients, stringent quality control, and a manufacturing process that's second-to-none. After all, at USANA we make more than just nutritionals--we help others create their USANA lifestyle. And we are able to do that with teams of incredible employees based around the world. USANA employees do more than work for our company--we embody the culture, and we live our company values: Excellence, Integrity, Health, and Community. We are committed to doing whatever it takes to ensure USANA's direct-selling Associates are supplied with whatever they need to become successful.
Mar 30, 2020
Full time
Quality Control Lab Analyst Location Salt Lake City Department Quality & Regulatory Affairs Apply Now USANA Health Sciences is seeking a dedicated and reliable individual to join the quality control laboratoryas a laboratory associate. In this position, you will perform chemical, physical and/or microbiological assays of raw materials and products to ensure they meet the quality standards established by the company. In this entry-level position, you will perform routine quality testing of products. This may include chemical identification testing, pH, particle size analysis, titrations, and HPLC analysis. Your ability to organize work assignments to complete testing in a timely manner will be integral to your success. As you develop in this position, you will participate in a leading laboratory in the industry. Our team works hard at creating a fun work environment and the experience gained in the quality control laboratory can open up doors to move into other positions both in the laboratory as well as in other areas of the company. A successful individual in this position will exemplify USANA's core values and must be self-motivated to produce quality work they can be proud of. Additional Essential Functions Conduct routine experiments and/or analyses Ability to follow written lab procedures Document results of experiments and analyses in notebooks and electronic spreadsheets Operate and maintain lab equipment Understand and adhere to GMP policies and procedures Perform other duties as assigned or needed Qualifications/Knowledge, Skills, and Abilities Requirements Associate's degree in science related field or 2- 5 years professional laboratory experience; Bachelor's degree preferred Must exhibit proficiency in basic laboratory skills and safety practices Ability to perform basic math functions Ability to efficiently and effectively perform all essential position duties and responsibilities with or without reasonable accommodation We've been around a while. We've done some amazing things. We've climbed to the top of the nutritional supplement industry, touching millions of lives along the way. Founded in 1992 by Dr. Myron Wentz, USANA Health Sciences is a U.S.-based international company that manufactures high-quality supplements, personal care, and energy products in our FDA-registered facility in Salt Lake City, Utah. USANA is committed to making the highest quality products without compromise. That's why we use only the purest ingredients, stringent quality control, and a manufacturing process that's second-to-none. After all, at USANA we make more than just nutritionals--we help others create their USANA lifestyle. And we are able to do that with teams of incredible employees based around the world. USANA employees do more than work for our company--we embody the culture, and we live our company values: Excellence, Integrity, Health, and Community. We are committed to doing whatever it takes to ensure USANA's direct-selling Associates are supplied with whatever they need to become successful.
HematoLogics, Inc. has a post-doctoral scientist opening in our Molecular Diagnostics department of our CAP-certified waterfront Seattle reference laboratory. The post-doctoral scientist will be part of our Molecular Diagnostics team and participate in daily wet-lab and analysis tasks. In addition, this position will contribute to research and development projects, focusing on the inter-disciplinary application of residual disease monitoring assays and their clinical utility in leukemia. Participation in the preparation of manuscript(s) to be published in peer-reviewed research journals is expected. The contract term of this position is 12 months. The ideal candidate should have a passion for clinical oncology research that will support and advance high-quality and industry-leading clinical laboratory diagnostic services and patient care. Next generation sequencing experience is required. Oncology or hematopathology experience is a plus. Attention to detail, high-complexity technical and inter-personal skill sets to participate in an interdisciplinary team-work setting (flow cytometry, cytogenetics, FISH, microarray, RT-PCR, Sanger, NGS, morphology) are desirable. HematoLogics, Inc. is a privately owned medical practice with a unique combination of academic pursuit and scientific discovery. We have developed an international reputation in the study of myelodysplasia, minimal disease detection, and integration of multiple technologies to detect and monitor treatment of hematologic diseases. We have established international collaborations and clinical trials to validate our approaches and assure that these innovative techniques and technologies will fit into the routine operation of a service oriented hematopathology referral group. Please submit your resume to: or HematoLogics, Inc. Attn. Barbara Zehentner, Ph.D. HCLD (ABB) 3161 Elliott Ave. Suite 200 Seattle, WA 98121
Mar 30, 2020
Full time
HematoLogics, Inc. has a post-doctoral scientist opening in our Molecular Diagnostics department of our CAP-certified waterfront Seattle reference laboratory. The post-doctoral scientist will be part of our Molecular Diagnostics team and participate in daily wet-lab and analysis tasks. In addition, this position will contribute to research and development projects, focusing on the inter-disciplinary application of residual disease monitoring assays and their clinical utility in leukemia. Participation in the preparation of manuscript(s) to be published in peer-reviewed research journals is expected. The contract term of this position is 12 months. The ideal candidate should have a passion for clinical oncology research that will support and advance high-quality and industry-leading clinical laboratory diagnostic services and patient care. Next generation sequencing experience is required. Oncology or hematopathology experience is a plus. Attention to detail, high-complexity technical and inter-personal skill sets to participate in an interdisciplinary team-work setting (flow cytometry, cytogenetics, FISH, microarray, RT-PCR, Sanger, NGS, morphology) are desirable. HematoLogics, Inc. is a privately owned medical practice with a unique combination of academic pursuit and scientific discovery. We have developed an international reputation in the study of myelodysplasia, minimal disease detection, and integration of multiple technologies to detect and monitor treatment of hematologic diseases. We have established international collaborations and clinical trials to validate our approaches and assure that these innovative techniques and technologies will fit into the routine operation of a service oriented hematopathology referral group. Please submit your resume to: or HematoLogics, Inc. Attn. Barbara Zehentner, Ph.D. HCLD (ABB) 3161 Elliott Ave. Suite 200 Seattle, WA 98121
Medicare Insurance Agent - Industry-best comp plan, total work freedom Join the revolutionary ASSURANCE platform, and earn from the industry's best comp plan, selling trusted Medicare plans to inbound, in-market shoppers. Get paid before, during, and after AEP. During AEP, we offer service fee commissions and bonuses, just for helping shoppers. Then after AEP, enjoy the largest January payout you've ever seen. Work as an independent, remote, contract agent. Enjoy the freedom of working when you want, from wherever you want, helping inbound, qualified, in-market shoppers - all free to you. Access our system, and eliminate agency inefficiencies and waste with free training, admin, support, product recommendations, and analytics. It's like Uber for insurance! After AEP, sell MediGap, health, or life, all year-round. Join the ASSURANCE agent network, and take advantage of these benefits: Free live, active, inbound shoppers generated from ASSURANCE-owned and operated sites Access to our proprietary system (includes no dialing, product recommendations, analytics, and constant platform improvement), at no cost to you Well-known and trusted carriers 100s of Guides prospecting for you Accessible underwriters A+ BBB-accredited and proven Requirements to access ASSURANCE platform: AHIP certification 12+ life insurance state licenses One year of phone sales experience High speed Internet connection, reliable computer, and headset with microphone Thorough understanding of HIPAA privacy and security laws, DNC, and insurance regulatory laws History of compliant insurance sales practice Working space and equipment that comply with HIPAA privacy and security standards About ASSURANCE: Everyone is unique. But insurance plans are not. Too often, plans offer blanket coverage, charging customers for coverage they don't need while not offering enough of what they do. ASSURANCE celebrates individual uniqueness with our personalized approach to seeking and purchasing insurance. Our platform serves as the intersection between customer and seller, technology and the human touch. We start by asking customers a few questions to learn about their needs. From there, our ground-breaking, proprietary platform analyzes the thousands of data points that make customers unique. This is how we create custom-tailored plans for each and every kind of customer; plans built precisely for their needs and budget. Our team of engineers, data scientists, marketers, architects, and designers are building systems using advanced science to make humans better. We're eliminating insurance industry waste and simplifying the complex. While our technology helps us personalize coverage, our network of experienced agents is how we deliver the right insurance to our customers. All ASSURANCE Medicare agents are 1099, independent contractors and have maximum control over how, where, and when they do their work. ASSURANCE simply provides the tools to make your business as successful as possible. Join ASSURANCE as we reimagine the role of insurance and enhance the personal and financial health of all consumers.
Mar 30, 2020
Full time
Medicare Insurance Agent - Industry-best comp plan, total work freedom Join the revolutionary ASSURANCE platform, and earn from the industry's best comp plan, selling trusted Medicare plans to inbound, in-market shoppers. Get paid before, during, and after AEP. During AEP, we offer service fee commissions and bonuses, just for helping shoppers. Then after AEP, enjoy the largest January payout you've ever seen. Work as an independent, remote, contract agent. Enjoy the freedom of working when you want, from wherever you want, helping inbound, qualified, in-market shoppers - all free to you. Access our system, and eliminate agency inefficiencies and waste with free training, admin, support, product recommendations, and analytics. It's like Uber for insurance! After AEP, sell MediGap, health, or life, all year-round. Join the ASSURANCE agent network, and take advantage of these benefits: Free live, active, inbound shoppers generated from ASSURANCE-owned and operated sites Access to our proprietary system (includes no dialing, product recommendations, analytics, and constant platform improvement), at no cost to you Well-known and trusted carriers 100s of Guides prospecting for you Accessible underwriters A+ BBB-accredited and proven Requirements to access ASSURANCE platform: AHIP certification 12+ life insurance state licenses One year of phone sales experience High speed Internet connection, reliable computer, and headset with microphone Thorough understanding of HIPAA privacy and security laws, DNC, and insurance regulatory laws History of compliant insurance sales practice Working space and equipment that comply with HIPAA privacy and security standards About ASSURANCE: Everyone is unique. But insurance plans are not. Too often, plans offer blanket coverage, charging customers for coverage they don't need while not offering enough of what they do. ASSURANCE celebrates individual uniqueness with our personalized approach to seeking and purchasing insurance. Our platform serves as the intersection between customer and seller, technology and the human touch. We start by asking customers a few questions to learn about their needs. From there, our ground-breaking, proprietary platform analyzes the thousands of data points that make customers unique. This is how we create custom-tailored plans for each and every kind of customer; plans built precisely for their needs and budget. Our team of engineers, data scientists, marketers, architects, and designers are building systems using advanced science to make humans better. We're eliminating insurance industry waste and simplifying the complex. While our technology helps us personalize coverage, our network of experienced agents is how we deliver the right insurance to our customers. All ASSURANCE Medicare agents are 1099, independent contractors and have maximum control over how, where, and when they do their work. ASSURANCE simply provides the tools to make your business as successful as possible. Join ASSURANCE as we reimagine the role of insurance and enhance the personal and financial health of all consumers.
Your Responsibilities The Chemist (Chem1) function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. Your Tasks Perform synthesis process including solution phase and solid phase peptide synthesis, peptide resin cleavage, resin cleavage with HF or other chemical cocktails Perform purification process by chromatography, crystallization and other techniques, and in-process test method Follow approved GMP manufacture directions such as Master Batch Records, Standard Operation Procedures, Standard Test Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities Perform project-planning and initiate raw material order-request. Receive raw materials, coordinate with QA/QC and Material Management for material release and monitor raw material inventories Install, test equipment, operate and maintain equipment for manufacturing and in-process testing. The equipment includes analytical HPLC and prep HPLC system, Lyophilizes, balances, reactors, HF cleavage equipment, diafiltration systems, water purification systems, oven, washing systems and others used in manufacture Develop processes for purification of chemicals other than peptides Follow and maintain GMP Documentation System. Investigate any process deviation and write process deviation report. Initiate document change request. Help quality control and assurance unit to maintain equipment calibration program Routinely maintain/organize work areas (Hood, bench, floor, wall, etc.) and other designated areas at the manufacturing facility Develop peptide-manufacturing processes including peptide/protein purification by chromatography, crystallization, and other techniques, and in process test methods Assist QA/QC for monitoring raw material inventories Write Standard Operation Procedures, Standard Test Procedures, Master Batch Records and other related GMP documents Follow SOPs and approved directions to clean equipment used in GMP processes, maintain cleaning log for each equipment, assist in equipment calibration program, and dispose chemical waste generated in the manufacture Monitor compliance of Maintenance and Cleaning procedures of equipment and instruments used in GMP processes by periodically reviewing and signing off on maintenance and cleaning log for each equipment Your Profile BS degree in Chemistry or related field 1-3 years' work experience Experience with HPLC and chromatography May work with hazardous materials and chemicals Excellent written and oral communication skills Basic computer knowledge, including Microsoft Word, Excel and PowerPoint Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues. Detail oriented with the ability to troubleshoot and resolve problems Ability to work independently and manage one's time Communicate effectively and ability to function well in a team environment Flexibility of working hours based on business needs, may include some nights and occasional weekends Preferred: Experience with Peptides General lab instrument (MS UV Spectrometry) knowledge and operation experience Knowledge of cGMP and FDA regulations We Offer You will be part of a motivated team overseeing the entire development cycle of respective APIs. If you are looking for a new challenge and want to join a motivated team in an internationally renowned company, you should seize this opportunity. Nearest Major Market: Los Angeles
Mar 30, 2020
Full time
Your Responsibilities The Chemist (Chem1) function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. Your Tasks Perform synthesis process including solution phase and solid phase peptide synthesis, peptide resin cleavage, resin cleavage with HF or other chemical cocktails Perform purification process by chromatography, crystallization and other techniques, and in-process test method Follow approved GMP manufacture directions such as Master Batch Records, Standard Operation Procedures, Standard Test Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities Perform project-planning and initiate raw material order-request. Receive raw materials, coordinate with QA/QC and Material Management for material release and monitor raw material inventories Install, test equipment, operate and maintain equipment for manufacturing and in-process testing. The equipment includes analytical HPLC and prep HPLC system, Lyophilizes, balances, reactors, HF cleavage equipment, diafiltration systems, water purification systems, oven, washing systems and others used in manufacture Develop processes for purification of chemicals other than peptides Follow and maintain GMP Documentation System. Investigate any process deviation and write process deviation report. Initiate document change request. Help quality control and assurance unit to maintain equipment calibration program Routinely maintain/organize work areas (Hood, bench, floor, wall, etc.) and other designated areas at the manufacturing facility Develop peptide-manufacturing processes including peptide/protein purification by chromatography, crystallization, and other techniques, and in process test methods Assist QA/QC for monitoring raw material inventories Write Standard Operation Procedures, Standard Test Procedures, Master Batch Records and other related GMP documents Follow SOPs and approved directions to clean equipment used in GMP processes, maintain cleaning log for each equipment, assist in equipment calibration program, and dispose chemical waste generated in the manufacture Monitor compliance of Maintenance and Cleaning procedures of equipment and instruments used in GMP processes by periodically reviewing and signing off on maintenance and cleaning log for each equipment Your Profile BS degree in Chemistry or related field 1-3 years' work experience Experience with HPLC and chromatography May work with hazardous materials and chemicals Excellent written and oral communication skills Basic computer knowledge, including Microsoft Word, Excel and PowerPoint Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues. Detail oriented with the ability to troubleshoot and resolve problems Ability to work independently and manage one's time Communicate effectively and ability to function well in a team environment Flexibility of working hours based on business needs, may include some nights and occasional weekends Preferred: Experience with Peptides General lab instrument (MS UV Spectrometry) knowledge and operation experience Knowledge of cGMP and FDA regulations We Offer You will be part of a motivated team overseeing the entire development cycle of respective APIs. If you are looking for a new challenge and want to join a motivated team in an internationally renowned company, you should seize this opportunity. Nearest Major Market: Los Angeles
Quality Control FULL-TIME $16/hr Responsible for quality checking products after they have been completed and ensure they are properly prepared for shipping.Duties include:Quality check all parts to match drawings before shipment to customerQuality controlMeasure parts and cross-reference to the prints to insure they are within tolerancesAccount for all the parts needed to complete the jobLabeling products with part numbers and serial numbers and documentLeak test products that are required to be leak proof and fill out proper documentation of resultsLoad and unload products and materials, making sure that all paperwork is filled out and distributed to the correct partiesPackage parts in a secure manner so able to be shipped without damage to the product PDX-01 WS-01 WS-LC Schedule Shift start: 8:00AM Shift length: 8 hours Monday - Friday, 8am - 5pm Benefits Health, dental, vision insurance - available after 60 days Paid time off 401(k) plan Qualifications Must pass drug screen Can lift 50 lbs Must be at least 18+ years old Ability to read and understand blueprintsAbility to operate forklifts and move pallet jacks of up to 150 lbs.Have attention to details and able to use basic math skills. About BBF Technologies We are a leading plastic fabrication company located in the Great Northwest. From wet process equipment to carts to chemical delivery systems, we design plastic and stainless steel equipment for some of the world s largest clean rooms and industrial plants. Associated topics: criteria, defect, qa, quality, quality assurance, quality check, quality control, quality manager, quality technician, test
Mar 30, 2020
Full time
Quality Control FULL-TIME $16/hr Responsible for quality checking products after they have been completed and ensure they are properly prepared for shipping.Duties include:Quality check all parts to match drawings before shipment to customerQuality controlMeasure parts and cross-reference to the prints to insure they are within tolerancesAccount for all the parts needed to complete the jobLabeling products with part numbers and serial numbers and documentLeak test products that are required to be leak proof and fill out proper documentation of resultsLoad and unload products and materials, making sure that all paperwork is filled out and distributed to the correct partiesPackage parts in a secure manner so able to be shipped without damage to the product PDX-01 WS-01 WS-LC Schedule Shift start: 8:00AM Shift length: 8 hours Monday - Friday, 8am - 5pm Benefits Health, dental, vision insurance - available after 60 days Paid time off 401(k) plan Qualifications Must pass drug screen Can lift 50 lbs Must be at least 18+ years old Ability to read and understand blueprintsAbility to operate forklifts and move pallet jacks of up to 150 lbs.Have attention to details and able to use basic math skills. About BBF Technologies We are a leading plastic fabrication company located in the Great Northwest. From wet process equipment to carts to chemical delivery systems, we design plastic and stainless steel equipment for some of the world s largest clean rooms and industrial plants. Associated topics: criteria, defect, qa, quality, quality assurance, quality check, quality control, quality manager, quality technician, test
Wisent USA , a well established manufacturer of cell culture and molecular biology products is looking for a motivated individual to promote its products in the Boston Area. A great entry level to mid level position with potential to become a managing position. Cell culture / molecular biology knowledge is required but sales kowledge is not. Position duties includes identifing and visiting customers as well as preparing reports and databases. We are also looking for an experienced manager with sales experience in the boston area. Cell culture knowledge is a must.
Mar 30, 2020
Full time
Wisent USA , a well established manufacturer of cell culture and molecular biology products is looking for a motivated individual to promote its products in the Boston Area. A great entry level to mid level position with potential to become a managing position. Cell culture / molecular biology knowledge is required but sales kowledge is not. Position duties includes identifing and visiting customers as well as preparing reports and databases. We are also looking for an experienced manager with sales experience in the boston area. Cell culture knowledge is a must.
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that I agree with Takeda's Privacy Notice , Privacy Policy and Terms of Use . Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Director, Data Services Analytics in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Here, you will be a vital contributor to our inspiring, bold mission. POSITION OBJECTIVES: The director of data services analytics will be responsible for the adoption and utilization of technologies, models and methods for science driven analytics of data services and architectures across R&D. Responsibilities will include: Shape and assess data architectures and services through data analytics for cell therapies and other current and emerging therapeutic areas across Takeda R&D from multiple dimensions including pre-clinical and discovery data, operational and clinical trial data, clinical production data, real world data, scientific data, and related. Lead the implementation and operational analytics of data services including performance, usage, governance, and management processes that reveal opportunities, insights, and approaches for data usage. Drive the definition, design, implementation and validation of cutting-edge algorithms to analyze diverse sources of data to achieve actionable design, planning, and improvement of data services by leveraging new data architectures, complex statistical and predictive modeling concepts, machine-learning approaches, clustering and classification techniques. Prioritize and oversee a portfolio of projects ensuring alignment of activities and standards. Measure, monitor, and collaborate with users, partners, and stakeholders on the use and socialization of techniques and new technologies throughout organization. POSITION ACCOUNTABILITIES: Oversee the ingestion and classification of diverse data sources, such as performance data, usage, adoption, health and status, and scientific data more broadly for cell therapies and other R&D areas. Deliver on data-driven projects through organization of team efforts and hands-on approach. Actively listen, integrate input from diverse sources, and collaboratively translate engineering, scientific, or business questions into data and analysis requirements Partner with experts to verify and drive model capabilities and translate modeling outputs into functional descriptions and business language. Partners with IT resources to enable and measure data flow, performance, reliability, development using appropriate tools/technology and rapid prototyping that informs the design of analytical products. Coach, develop and mentor others on data services analytics, tools and methodologies. Build external alliances to gain and share new insights from architecture analysis, technical information, and trends both internal and external. EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS: Advanced degree or equivalent experience in computer science, mathematics, or a data-related field with a substantial software architecture, design, and scientific rigor emphasis. Experience working in industrial-scale projects with experience in pharmaceutical / biotechnology / healthcare / health IT industry a desirable. Demonstrated experience in exploring alternate approaches and novel solutions Strong management and organizational skills. Ability to effectively interact with and influence all levels of management. Seasoned computer scientist or data scientist with experience in large-scale healthcare data analysis and industry models/standards. Expertise in advanced data architectures and deep knowledge of a wide range of analytic approaches, computing models, and data structures. Advanced hands-on knowledge of advanced database technologies, graph structures, modern software languages, full stack development, analytic environments, and devops tools. Experience analyzing data from traditional healthcare databases or similar structured and unstructured datasets. Experience with big data methodologies and cloud environments. TRAVEL REQUIREMENTS: Willingness to travel to various meetings, corporate partners, additional Takeda sites. Requires approximately 10% travel. WHAT TAKEDA CAN OFFER YOU: 401(k) with company match and Annual Retirement Contribution Plan Tuition reimbursement Company match of charitable contributions Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs Empowering Our People to Shine Discover more at takedajobs.com No Phone Calls or Recruiters Please. #LI-SGM Locations Boston, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time
Mar 30, 2020
Full time
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that I agree with Takeda's Privacy Notice , Privacy Policy and Terms of Use . Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Director, Data Services Analytics in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Here, you will be a vital contributor to our inspiring, bold mission. POSITION OBJECTIVES: The director of data services analytics will be responsible for the adoption and utilization of technologies, models and methods for science driven analytics of data services and architectures across R&D. Responsibilities will include: Shape and assess data architectures and services through data analytics for cell therapies and other current and emerging therapeutic areas across Takeda R&D from multiple dimensions including pre-clinical and discovery data, operational and clinical trial data, clinical production data, real world data, scientific data, and related. Lead the implementation and operational analytics of data services including performance, usage, governance, and management processes that reveal opportunities, insights, and approaches for data usage. Drive the definition, design, implementation and validation of cutting-edge algorithms to analyze diverse sources of data to achieve actionable design, planning, and improvement of data services by leveraging new data architectures, complex statistical and predictive modeling concepts, machine-learning approaches, clustering and classification techniques. Prioritize and oversee a portfolio of projects ensuring alignment of activities and standards. Measure, monitor, and collaborate with users, partners, and stakeholders on the use and socialization of techniques and new technologies throughout organization. POSITION ACCOUNTABILITIES: Oversee the ingestion and classification of diverse data sources, such as performance data, usage, adoption, health and status, and scientific data more broadly for cell therapies and other R&D areas. Deliver on data-driven projects through organization of team efforts and hands-on approach. Actively listen, integrate input from diverse sources, and collaboratively translate engineering, scientific, or business questions into data and analysis requirements Partner with experts to verify and drive model capabilities and translate modeling outputs into functional descriptions and business language. Partners with IT resources to enable and measure data flow, performance, reliability, development using appropriate tools/technology and rapid prototyping that informs the design of analytical products. Coach, develop and mentor others on data services analytics, tools and methodologies. Build external alliances to gain and share new insights from architecture analysis, technical information, and trends both internal and external. EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS: Advanced degree or equivalent experience in computer science, mathematics, or a data-related field with a substantial software architecture, design, and scientific rigor emphasis. Experience working in industrial-scale projects with experience in pharmaceutical / biotechnology / healthcare / health IT industry a desirable. Demonstrated experience in exploring alternate approaches and novel solutions Strong management and organizational skills. Ability to effectively interact with and influence all levels of management. Seasoned computer scientist or data scientist with experience in large-scale healthcare data analysis and industry models/standards. Expertise in advanced data architectures and deep knowledge of a wide range of analytic approaches, computing models, and data structures. Advanced hands-on knowledge of advanced database technologies, graph structures, modern software languages, full stack development, analytic environments, and devops tools. Experience analyzing data from traditional healthcare databases or similar structured and unstructured datasets. Experience with big data methodologies and cloud environments. TRAVEL REQUIREMENTS: Willingness to travel to various meetings, corporate partners, additional Takeda sites. Requires approximately 10% travel. WHAT TAKEDA CAN OFFER YOU: 401(k) with company match and Annual Retirement Contribution Plan Tuition reimbursement Company match of charitable contributions Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs Empowering Our People to Shine Discover more at takedajobs.com No Phone Calls or Recruiters Please. #LI-SGM Locations Boston, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time
Rentschler Biopharma, headquartered in Laupheim, Germany, is a leading contract development and manufacturing organization (CDMO), focused exclusively on client projects. Rentschler Biopharma offers process development and manufacturing of biopharmaceuticals as well as related consulting activities, including project management and regulatory support. Rentschler recently expanded its global footprint by opening a facility in the Boston metro area in Milford, MA. This new site answers our US clients' strong request to bring our expertise, innovation and state of the art, high-quality development and manufacturing across the Atlantic to better serve the unique US market, a key market for Rentschler Biopharma. Milford's proximity to our key US clients and Boston metro's many biotech startups, large pharmaceutical companies, incubator sites, world-class universities and biotech-focused research institutions enable us to strengthen our important US partnerships and forge new ones, elevate our technological capabilities and tap into the region's wide pool of expert talent. Rentschler Biopharma, Inc. is recruiting for a proactive, dynamic and "hands-on", Director / Senior Director Business Development. This is an exciting opportunity for a highly experienced and ambitious professional to take on a pivotal role within an innovative CDMO organisation at a time of critical growth. The Director / Senior Director represents a critical hire for Rentschler Biopharma; essential in securing the future success of global expansion. As such the role will benefit from high visibility both internally and externally. Building trustworthy relationships with key internal and external stakeholders will be paramount to your success. Rentschler Biopharma has ambitious plans for growth and as a key executive within the organization, there are multiple long-term development opportunities for the right candidate based on performance and career aspirations. OPPORTUNITY HIGHLIGHTS · Unique opportunity to join a fast-growing, entrepreneurial CDMO and be a key member in their transition from good to great · Creativity and out of the box thinking are encouraged at Rentschler Biopharma so you will be working in an open culture that promotes innovation · You will have the opportunity and autonomy to shape the role and ensure it meets the business and customer needs · This role is a key priority for the organization providing you with the opportunity to hold a broad mandate driving business development activity globally for Rentschler Biopharma · This is an opportunity to join Rentschler Biopharma at a key time of their development and be part of an exciting journey with a cutting-edge organization that is a leader in the CDMO industry Duties and Responsibilities · Drive short to long term business development strategy · Represent Rentschler Biopharma to clients and play an ambassadorial role within a global market. · Act as a strategic partner to clients, providing strategic solution to complex requirements and unmet needs. · Identify and develop new business opportunities resulting in active acquisition of new major clients and new contracts from existing clients · Active support of existing clients and their new projects · Solicit requests for proposals (RFPs), requests for information (RFIs), requests for quotations (RFQs), etc. from existing and new clients · Drive sales processes initial contact to contract execution · Drive revenue and market share growth · Lead all aspects of business development including marketing efforts, strategic planning, budgeting and forecasting · Initiation and co-ordination of customer visits with functional departments to facilitate the conclusion of contracts for strategic partnerships · Confident representation of the Rentschler brand towards key customers to contribute to a sustainable branding of Rentschler as competent CDMO · Own all processes and responses as needed to support client inquires. Utilize designated CRM to track and follow up on all client leads, query department productivity reports and build trend reports · Develop, update, maintain and evaluate competitive and industry analysis and intelligence information/database, ensuring the monitoring of international biopharmaceutical markets and incorporation of the insights into the corporate radar · Formulate value proposition story based on client opportunities, competitor behaviors, marketplace dynamics and trends, pricing segmentation and practices, productions costs, competitive positions, and marketing programs · Analyze existing customer sales data combined with understanding external market data to deliver the "outside-in" perspective to help further drive revenue and profitability · Ensure that international markets for biopharmaceuticals are observed and incorporation of the knowledge acquired into the Corporate Rader of Rentschler to detect new technologies for Rentschler and to identify substitute technologies · Representation of the company at international fairs and monitoring global markets · Build a collaborative working relationship with cross-functional peers · Act as a subject matter expert to support internal and external stakeholders Qualifications · BD, MS, Ph.D. from an accredited college or university with a focus in biotechnology, biology · Must be proficient in Microsoft Office applications and CRM platforms · 5+ years of industrial experience in production and/or bioprocess services sales, business development and/or marketing functions within life science technology companies preferably in selling contract development/production (CDMO/CMO/CRO) · Demonstrated experience in leading sales and business growth through prospecting new partners, generating leads, and growing and maintaining existing partner relationships to foster partnership expansion · Extensive experience in selling complex services for the biological/pharmaceutical industry · In depth experience with business and/or supply negotiations compulsory · Experience in managing relationships and long-term strategic partnerships to ensure alignment with the partner and corporate objectives including coordination with key internal stakeholders · Strong understanding of the whole value chain from gene, formulation, DS/DP production and beyond · Deep knowledge of the drug development process, project management and pharmaceutical regulatory environments. Knowledge of FDA/EMEA CMC requirements and submission processes preferred · Experience developing market analysis and action plans to drive partnership growth · Able to work in a highly international multifunctional framework · Demonstrated record of creative, flexible, and pragmatic approach to business development with a strong partnership-focused mentality combined · An entrepreneurial mindset with a convincing and winning appearance to clients · Willingness to take on a position with intensive travelling Rentschler Biopharma, Inc. offers a competitive compensation package to include major medical/dental/vision, group life insurance, STD/LTD plans, 401k plan with company match, and paid vacation, sick and holidays. Rentschler Biopharma, Inc. is an Equal Opportunity Employer: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Mar 30, 2020
Full time
Rentschler Biopharma, headquartered in Laupheim, Germany, is a leading contract development and manufacturing organization (CDMO), focused exclusively on client projects. Rentschler Biopharma offers process development and manufacturing of biopharmaceuticals as well as related consulting activities, including project management and regulatory support. Rentschler recently expanded its global footprint by opening a facility in the Boston metro area in Milford, MA. This new site answers our US clients' strong request to bring our expertise, innovation and state of the art, high-quality development and manufacturing across the Atlantic to better serve the unique US market, a key market for Rentschler Biopharma. Milford's proximity to our key US clients and Boston metro's many biotech startups, large pharmaceutical companies, incubator sites, world-class universities and biotech-focused research institutions enable us to strengthen our important US partnerships and forge new ones, elevate our technological capabilities and tap into the region's wide pool of expert talent. Rentschler Biopharma, Inc. is recruiting for a proactive, dynamic and "hands-on", Director / Senior Director Business Development. This is an exciting opportunity for a highly experienced and ambitious professional to take on a pivotal role within an innovative CDMO organisation at a time of critical growth. The Director / Senior Director represents a critical hire for Rentschler Biopharma; essential in securing the future success of global expansion. As such the role will benefit from high visibility both internally and externally. Building trustworthy relationships with key internal and external stakeholders will be paramount to your success. Rentschler Biopharma has ambitious plans for growth and as a key executive within the organization, there are multiple long-term development opportunities for the right candidate based on performance and career aspirations. OPPORTUNITY HIGHLIGHTS · Unique opportunity to join a fast-growing, entrepreneurial CDMO and be a key member in their transition from good to great · Creativity and out of the box thinking are encouraged at Rentschler Biopharma so you will be working in an open culture that promotes innovation · You will have the opportunity and autonomy to shape the role and ensure it meets the business and customer needs · This role is a key priority for the organization providing you with the opportunity to hold a broad mandate driving business development activity globally for Rentschler Biopharma · This is an opportunity to join Rentschler Biopharma at a key time of their development and be part of an exciting journey with a cutting-edge organization that is a leader in the CDMO industry Duties and Responsibilities · Drive short to long term business development strategy · Represent Rentschler Biopharma to clients and play an ambassadorial role within a global market. · Act as a strategic partner to clients, providing strategic solution to complex requirements and unmet needs. · Identify and develop new business opportunities resulting in active acquisition of new major clients and new contracts from existing clients · Active support of existing clients and their new projects · Solicit requests for proposals (RFPs), requests for information (RFIs), requests for quotations (RFQs), etc. from existing and new clients · Drive sales processes initial contact to contract execution · Drive revenue and market share growth · Lead all aspects of business development including marketing efforts, strategic planning, budgeting and forecasting · Initiation and co-ordination of customer visits with functional departments to facilitate the conclusion of contracts for strategic partnerships · Confident representation of the Rentschler brand towards key customers to contribute to a sustainable branding of Rentschler as competent CDMO · Own all processes and responses as needed to support client inquires. Utilize designated CRM to track and follow up on all client leads, query department productivity reports and build trend reports · Develop, update, maintain and evaluate competitive and industry analysis and intelligence information/database, ensuring the monitoring of international biopharmaceutical markets and incorporation of the insights into the corporate radar · Formulate value proposition story based on client opportunities, competitor behaviors, marketplace dynamics and trends, pricing segmentation and practices, productions costs, competitive positions, and marketing programs · Analyze existing customer sales data combined with understanding external market data to deliver the "outside-in" perspective to help further drive revenue and profitability · Ensure that international markets for biopharmaceuticals are observed and incorporation of the knowledge acquired into the Corporate Rader of Rentschler to detect new technologies for Rentschler and to identify substitute technologies · Representation of the company at international fairs and monitoring global markets · Build a collaborative working relationship with cross-functional peers · Act as a subject matter expert to support internal and external stakeholders Qualifications · BD, MS, Ph.D. from an accredited college or university with a focus in biotechnology, biology · Must be proficient in Microsoft Office applications and CRM platforms · 5+ years of industrial experience in production and/or bioprocess services sales, business development and/or marketing functions within life science technology companies preferably in selling contract development/production (CDMO/CMO/CRO) · Demonstrated experience in leading sales and business growth through prospecting new partners, generating leads, and growing and maintaining existing partner relationships to foster partnership expansion · Extensive experience in selling complex services for the biological/pharmaceutical industry · In depth experience with business and/or supply negotiations compulsory · Experience in managing relationships and long-term strategic partnerships to ensure alignment with the partner and corporate objectives including coordination with key internal stakeholders · Strong understanding of the whole value chain from gene, formulation, DS/DP production and beyond · Deep knowledge of the drug development process, project management and pharmaceutical regulatory environments. Knowledge of FDA/EMEA CMC requirements and submission processes preferred · Experience developing market analysis and action plans to drive partnership growth · Able to work in a highly international multifunctional framework · Demonstrated record of creative, flexible, and pragmatic approach to business development with a strong partnership-focused mentality combined · An entrepreneurial mindset with a convincing and winning appearance to clients · Willingness to take on a position with intensive travelling Rentschler Biopharma, Inc. offers a competitive compensation package to include major medical/dental/vision, group life insurance, STD/LTD plans, 401k plan with company match, and paid vacation, sick and holidays. Rentschler Biopharma, Inc. is an Equal Opportunity Employer: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Sr. Development Scientist - Pulp Location: Memphis, TN Travel: Less than 10% Position Summary: The Development Scientist in Pulp will contribute to Buckman's Global Growth Strategy by accelerating the development of new products and increasing foundational knowledge on predictive laboratory performance testing and evaluation for pulp related chemistries. The resource will be positioned to maintain existing projects and accelerate the development of new capabilities in BSW defoamers, digester additives, and drive the development of new digital capabilities to support current and future new products. This position will be application and formulation focused and will be expected to deliver new, differentiated technologies that grow Buckman's market share in pulp related markets. Competencies Needed for Success: • Demonstrated excellence in laboratory safety practices and compliance • Hands on experience formulating and scaling up defoamer based technologies; Strong formulation and emulsion chemistry knowledge • Must have experience and knowledge of pulp applications and product performance characterization, e.g. application testing knowledge and instrumentation • Successfully have developed and supported new products for pulp markets • Experience supporting product scale-up, manufacturing, and product trials • Planning, preparing and executing design of experiments and project plans • Pulp and BSW defoamer application testing knowledge and instrumentation • Versatile skills that bridge hardware, software and chemistry to create innovative solutions • A thorough understanding of scientific methodology and working understanding of laboratory operations, laboratory instrumentation, and laboratory methods is required • Track record of new product development from concept to commercialization • Experienced in operation and maintenance of analytical and application testing instruments • Must have good communication skills, both written and verbal, and can work independently and on multidisciplinary teams Minimum Requirements to Apply: Ph.D. in Chemistry, Chemical Engineering, Material Science, Applied Surfactant Science, Colloid or Physical Chemistry with 2+ years of experience in relevant industry, or M. S. degree with 5+ years of experience in relevant industry. A secondary degree in applied Pulp/Paper Science with primary degree in chemical related field would be considered. Direct experience and knowledge in pulp related platform chemistries and defoamers is highly desired. Experience with emulsions and direct scale-up is required.
Mar 30, 2020
Full time
Sr. Development Scientist - Pulp Location: Memphis, TN Travel: Less than 10% Position Summary: The Development Scientist in Pulp will contribute to Buckman's Global Growth Strategy by accelerating the development of new products and increasing foundational knowledge on predictive laboratory performance testing and evaluation for pulp related chemistries. The resource will be positioned to maintain existing projects and accelerate the development of new capabilities in BSW defoamers, digester additives, and drive the development of new digital capabilities to support current and future new products. This position will be application and formulation focused and will be expected to deliver new, differentiated technologies that grow Buckman's market share in pulp related markets. Competencies Needed for Success: • Demonstrated excellence in laboratory safety practices and compliance • Hands on experience formulating and scaling up defoamer based technologies; Strong formulation and emulsion chemistry knowledge • Must have experience and knowledge of pulp applications and product performance characterization, e.g. application testing knowledge and instrumentation • Successfully have developed and supported new products for pulp markets • Experience supporting product scale-up, manufacturing, and product trials • Planning, preparing and executing design of experiments and project plans • Pulp and BSW defoamer application testing knowledge and instrumentation • Versatile skills that bridge hardware, software and chemistry to create innovative solutions • A thorough understanding of scientific methodology and working understanding of laboratory operations, laboratory instrumentation, and laboratory methods is required • Track record of new product development from concept to commercialization • Experienced in operation and maintenance of analytical and application testing instruments • Must have good communication skills, both written and verbal, and can work independently and on multidisciplinary teams Minimum Requirements to Apply: Ph.D. in Chemistry, Chemical Engineering, Material Science, Applied Surfactant Science, Colloid or Physical Chemistry with 2+ years of experience in relevant industry, or M. S. degree with 5+ years of experience in relevant industry. A secondary degree in applied Pulp/Paper Science with primary degree in chemical related field would be considered. Direct experience and knowledge in pulp related platform chemistries and defoamers is highly desired. Experience with emulsions and direct scale-up is required.
Job Success Profile Biotechnology Research Scientist 1. Mission Statement Contributes to the success of Buckman's product offerings through development of enzymatic technologies that create new and valuable outcomes for our customers. This position will primarily support Buckman's Global Growth Strategy efforts as well as provide formulation support for continuous improvement efforts. 2. Outcomes Leads and successfully completes global projects (new applications, retrofits, etc.) throughout the entire life cycle of product development (idea generation, rapid prototyping to develop promising candidates, product development, and commercial deployment) that positively impact the customer experience and increase the adoption of Buckman's solutions. Successfully manages external partners to ensure that Buckman's business needs are met considering time, quality and cost. Provides technical coaching to associates on enzymatic R&D areas and project facilitation to ensure that knowledge and practices are successfully shared and learned. Proactively identifies and promotes innovative solutions that have a broad, organizational impact (e.g., profitability, sales, efficiency). Takes the initiative to learn innovative methods, tools, and technology and show others how they can be applied to work tasks. 3. Responsibilities The design, characterization and evaluation of new products using traditional and new approaches targeting key markets. Identification and utilization of novel molecules in enzymatic technologies. Support formulation efforts for next-generation enzymatic technologies, including expression and characterization studies. Contribute to a strong and active portfolio of intellectual property. Support the adoption of new technologies by supporting field trials and crafting engaging conference presentations. Work with other teams within Buckman to support their needs for new, high performance products. 4. Main Success Metrics Percentage complete of Key Performance Measures (KPMs) considering key measures of success. Project completion (considering time, quality and cost). Adoption and usage of new product chemistries at Buckman's customer production facilities. 5. Competencies: Job Competencies - Results Leadership: Focus on Results - Consistently achieving results, even under tough circumstances. Action Oriented - Taking on new opportunities and tough challenges with a sense of urgency, high energy and enthusiasm. Plans and Aligns - Planning and prioritizing work to meet commitments aligned with organizational goals. Ensures Accountability - Holding self and others accountable to meet commitments. Job Competencies - People Leadership: Collaborates - Building partnerships and working collaboratively with others to meet shared objectives. Job Competencies - Thought Leadership: Managing Complexity - Making sense of complex, high quantity, and sometimes contradictory information to effectively solve problems. Possibility Thinking - Creating new and better ways for the organization to be successful. Customer Focus - Building strong customer relationships and delivering customer-centric solutions. Job Competencies - Self Leadership: Nimble Learning - Actively learning through experimentation when tackling new problems, using both successes and failures as learning fodder. 6. Minimum requirement to apply Must have had successful experiences: BSc in a biological discipline with 15 years of experience MSc in a biological discipline with 10 years of experience PhD (preferred) in biological discipline with 3+ years of experience. At least 3 years practical experience in the area of enzyme expression, characterization and formulation. Experience in the scale-up of enzyme manufacture beyond 10L scale. >1 year of industrial enzyme application experience. Preference given to individuals who have: Practical experience in paper/pulp technology development, including physical property testing. Must have these Competencies: Required Competencies Collaborates Focus on Results Manages Complexity Nimble Learning Technical Job Knowledge (Choose from drop downs) Possibility Thinking Action Oriented Location: Memphis, Tennessee Language: English Travel:
Mar 30, 2020
Full time
Job Success Profile Biotechnology Research Scientist 1. Mission Statement Contributes to the success of Buckman's product offerings through development of enzymatic technologies that create new and valuable outcomes for our customers. This position will primarily support Buckman's Global Growth Strategy efforts as well as provide formulation support for continuous improvement efforts. 2. Outcomes Leads and successfully completes global projects (new applications, retrofits, etc.) throughout the entire life cycle of product development (idea generation, rapid prototyping to develop promising candidates, product development, and commercial deployment) that positively impact the customer experience and increase the adoption of Buckman's solutions. Successfully manages external partners to ensure that Buckman's business needs are met considering time, quality and cost. Provides technical coaching to associates on enzymatic R&D areas and project facilitation to ensure that knowledge and practices are successfully shared and learned. Proactively identifies and promotes innovative solutions that have a broad, organizational impact (e.g., profitability, sales, efficiency). Takes the initiative to learn innovative methods, tools, and technology and show others how they can be applied to work tasks. 3. Responsibilities The design, characterization and evaluation of new products using traditional and new approaches targeting key markets. Identification and utilization of novel molecules in enzymatic technologies. Support formulation efforts for next-generation enzymatic technologies, including expression and characterization studies. Contribute to a strong and active portfolio of intellectual property. Support the adoption of new technologies by supporting field trials and crafting engaging conference presentations. Work with other teams within Buckman to support their needs for new, high performance products. 4. Main Success Metrics Percentage complete of Key Performance Measures (KPMs) considering key measures of success. Project completion (considering time, quality and cost). Adoption and usage of new product chemistries at Buckman's customer production facilities. 5. Competencies: Job Competencies - Results Leadership: Focus on Results - Consistently achieving results, even under tough circumstances. Action Oriented - Taking on new opportunities and tough challenges with a sense of urgency, high energy and enthusiasm. Plans and Aligns - Planning and prioritizing work to meet commitments aligned with organizational goals. Ensures Accountability - Holding self and others accountable to meet commitments. Job Competencies - People Leadership: Collaborates - Building partnerships and working collaboratively with others to meet shared objectives. Job Competencies - Thought Leadership: Managing Complexity - Making sense of complex, high quantity, and sometimes contradictory information to effectively solve problems. Possibility Thinking - Creating new and better ways for the organization to be successful. Customer Focus - Building strong customer relationships and delivering customer-centric solutions. Job Competencies - Self Leadership: Nimble Learning - Actively learning through experimentation when tackling new problems, using both successes and failures as learning fodder. 6. Minimum requirement to apply Must have had successful experiences: BSc in a biological discipline with 15 years of experience MSc in a biological discipline with 10 years of experience PhD (preferred) in biological discipline with 3+ years of experience. At least 3 years practical experience in the area of enzyme expression, characterization and formulation. Experience in the scale-up of enzyme manufacture beyond 10L scale. >1 year of industrial enzyme application experience. Preference given to individuals who have: Practical experience in paper/pulp technology development, including physical property testing. Must have these Competencies: Required Competencies Collaborates Focus on Results Manages Complexity Nimble Learning Technical Job Knowledge (Choose from drop downs) Possibility Thinking Action Oriented Location: Memphis, Tennessee Language: English Travel:
Job Description Position Overview: Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalent's advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents , ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Interested in learning more about life at Catalent? Start here Catalent Paragon Gene Therapy is looking to recruit an Associate Scientist III - Downstream Process Development to join our growing team in Rockville, MD. The Associate Scientist III - Downstream Process Development will be responsible for process and product development within a dynamic project team. The ideal candidate will demonstrate strong technical knowledge, initiative, and scientific commitment, and make significant scientific and technical contributions within the Analytical Development Group as well as their project teams. The Associate Scientist III - Downstream Process Development role is critical to our patients. We develop manufacturing processes for life-changing therapies with patient safety in mind, executing with efficiency always. Quality, safety, and on-time delivery is a must to be successful in this role! Paragon Gene Therapy, now a part of Catalent, hires people with a passion to make a difference. Your expertise, coupled with our advanced technologies and collaboration with innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. The Role: Integral team member in moving projects forward toward GMP Manufacturing for clinical trials, registration, improvements of existing processes and products. Downstream process development of recombinant protein, virus-like particle, and virus from mammalian cells insect cells, or microbes. Deploys knowledge and technical skills to independently design and execute studies. Documents and effectively communicates results of individual executed work through summary presentations, discussions with his/her supervisor, and scientific meetings on a regular basis. Interaction with appropriate members of upstream, analytical and quality control functional areas for purification, analysis and review of documentation. Possesses considerable knowledge and expertise relating to protein purification and analysis and other fundamental lab technologies or platforms. The Candidate: B.S. in Life Science or Chemical Engineering with 5-7 years experience OR M.S. in Life Science or Chemical Engineering 3-5 years' experience in the Biotechnology or Pharmaceutical industry. Proficiency in chromatography-based processing methods such as Affinity, ION Exchange, Hydrophobic Interaction, and Size Exclusion chromatography, as well as methods for column packing, is required. Knowledge of how GMP regulations impact process development of biologics products. Ease with document writing, data interpretation, presentation skills, and statistical analysis. The ability to work in a team-oriented environment is essential, as this person will work closely with other members of the Process Development Group, QC, GMP, and will participate in multidisciplinary project teams. We will identify candidates based on the following: Leads with Integrity and Respect Delivers Results Demonstrates Business Acumen Fosters Collaboration and Teamwork Champions Change Engages and Inspires Coaches and Develops Position Benefits: Join a high growth and fast paced organization with a people focused culture Global exposure, defined career path and annual performance review and feedback process Competitive Medical, Dental, Vision and 401K Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit to explore career opportunities. Catalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Mar 30, 2020
Full time
Job Description Position Overview: Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalent's advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents , ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Interested in learning more about life at Catalent? Start here Catalent Paragon Gene Therapy is looking to recruit an Associate Scientist III - Downstream Process Development to join our growing team in Rockville, MD. The Associate Scientist III - Downstream Process Development will be responsible for process and product development within a dynamic project team. The ideal candidate will demonstrate strong technical knowledge, initiative, and scientific commitment, and make significant scientific and technical contributions within the Analytical Development Group as well as their project teams. The Associate Scientist III - Downstream Process Development role is critical to our patients. We develop manufacturing processes for life-changing therapies with patient safety in mind, executing with efficiency always. Quality, safety, and on-time delivery is a must to be successful in this role! Paragon Gene Therapy, now a part of Catalent, hires people with a passion to make a difference. Your expertise, coupled with our advanced technologies and collaboration with innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. The Role: Integral team member in moving projects forward toward GMP Manufacturing for clinical trials, registration, improvements of existing processes and products. Downstream process development of recombinant protein, virus-like particle, and virus from mammalian cells insect cells, or microbes. Deploys knowledge and technical skills to independently design and execute studies. Documents and effectively communicates results of individual executed work through summary presentations, discussions with his/her supervisor, and scientific meetings on a regular basis. Interaction with appropriate members of upstream, analytical and quality control functional areas for purification, analysis and review of documentation. Possesses considerable knowledge and expertise relating to protein purification and analysis and other fundamental lab technologies or platforms. The Candidate: B.S. in Life Science or Chemical Engineering with 5-7 years experience OR M.S. in Life Science or Chemical Engineering 3-5 years' experience in the Biotechnology or Pharmaceutical industry. Proficiency in chromatography-based processing methods such as Affinity, ION Exchange, Hydrophobic Interaction, and Size Exclusion chromatography, as well as methods for column packing, is required. Knowledge of how GMP regulations impact process development of biologics products. Ease with document writing, data interpretation, presentation skills, and statistical analysis. The ability to work in a team-oriented environment is essential, as this person will work closely with other members of the Process Development Group, QC, GMP, and will participate in multidisciplinary project teams. We will identify candidates based on the following: Leads with Integrity and Respect Delivers Results Demonstrates Business Acumen Fosters Collaboration and Teamwork Champions Change Engages and Inspires Coaches and Develops Position Benefits: Join a high growth and fast paced organization with a people focused culture Global exposure, defined career path and annual performance review and feedback process Competitive Medical, Dental, Vision and 401K Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit to explore career opportunities. Catalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Amgen is a leading global biotechnology company, with a mission to serve patients around the world. As a science-based, patient-focused organization, we discover and develop innovative therapies to treat serious illnesses. Our medicines have made a dramatic difference in the lives of millions. To underpin our commitment to serve patients, Amgen is hiring in the department of Medicinal Chemistry at our Research and Development facility in Thousand Oaks, CA (ATO). This Senior Scientist role will be part of an innovative Medicinal Chemistry group with responsibilities including (but not limited to) the design, synthesis, and purification of novel compounds for potential clinical drug development, including opportunity to work within Amgen's Induced Proximity Platform (IPP), which is focused on novel and innovative approaches to modulate intractable targets in diseases using the emerging PROTAC modality. The Senior Scientist may directly or indirectly manage research scientists and/or associates within a collaborative environment and be responsible for providing motivating professional development coaching within his/her group. Additional responsibilities include but are not limited to: devising and implementing creative scientific strategies to address synthetic and medicinal chemistry issues through conducting laboratory experiments, working closely with other researchers to influence team direction and advance programs, communicating progress and strategy in various forums, and preparing technical documents. The Senior Scientist will serve as a scientific resource to the department who will champion new technologies/ideas to enhance capabilities. Basic Qualifications Doctorate degree and 2 years of medicinal chemistry or pharmaceutical research experience OR Master's degree and 5 years of medicinal chemistry or pharmaceutical research experience OR Bachelor's degree and 7 years of medicinal chemistry or pharmaceutical research experience Preferred Qualifications Doctorate degree in chemistry specializing in organic synthesis 6+ years of experience in synthetic organic or medicinal chemistry Experience leading/participating on a team that has advanced compounds to clinical development Track record of consistent and successful drug discovery accomplishments (e.g., patent inventorship, conference presentations, and peer-reviewed publications) Deep understanding of synthetic and medicinal and chemistry concepts with high lab productivity Demonstration of good lab practices, with particular attention to safety Proficient skills in parallel synthesis and use of structure-based or other computer-aided design tools Broad understanding of drug discovery disciplines (e.g., chemistry, biology, safety, PKDM, etc.) Experience managing direct reports or coaching others (internal or CRO) Excellent communication skills (both written and oral), leadership skills and the ability to work well in teams Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology and is matched by an unparalleled toolbox of therapeutic modalities ranging from small molecules to peptides to proteins to antibodies to live cell-therapies. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Mar 30, 2020
Full time
Amgen is a leading global biotechnology company, with a mission to serve patients around the world. As a science-based, patient-focused organization, we discover and develop innovative therapies to treat serious illnesses. Our medicines have made a dramatic difference in the lives of millions. To underpin our commitment to serve patients, Amgen is hiring in the department of Medicinal Chemistry at our Research and Development facility in Thousand Oaks, CA (ATO). This Senior Scientist role will be part of an innovative Medicinal Chemistry group with responsibilities including (but not limited to) the design, synthesis, and purification of novel compounds for potential clinical drug development, including opportunity to work within Amgen's Induced Proximity Platform (IPP), which is focused on novel and innovative approaches to modulate intractable targets in diseases using the emerging PROTAC modality. The Senior Scientist may directly or indirectly manage research scientists and/or associates within a collaborative environment and be responsible for providing motivating professional development coaching within his/her group. Additional responsibilities include but are not limited to: devising and implementing creative scientific strategies to address synthetic and medicinal chemistry issues through conducting laboratory experiments, working closely with other researchers to influence team direction and advance programs, communicating progress and strategy in various forums, and preparing technical documents. The Senior Scientist will serve as a scientific resource to the department who will champion new technologies/ideas to enhance capabilities. Basic Qualifications Doctorate degree and 2 years of medicinal chemistry or pharmaceutical research experience OR Master's degree and 5 years of medicinal chemistry or pharmaceutical research experience OR Bachelor's degree and 7 years of medicinal chemistry or pharmaceutical research experience Preferred Qualifications Doctorate degree in chemistry specializing in organic synthesis 6+ years of experience in synthetic organic or medicinal chemistry Experience leading/participating on a team that has advanced compounds to clinical development Track record of consistent and successful drug discovery accomplishments (e.g., patent inventorship, conference presentations, and peer-reviewed publications) Deep understanding of synthetic and medicinal and chemistry concepts with high lab productivity Demonstration of good lab practices, with particular attention to safety Proficient skills in parallel synthesis and use of structure-based or other computer-aided design tools Broad understanding of drug discovery disciplines (e.g., chemistry, biology, safety, PKDM, etc.) Experience managing direct reports or coaching others (internal or CRO) Excellent communication skills (both written and oral), leadership skills and the ability to work well in teams Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology and is matched by an unparalleled toolbox of therapeutic modalities ranging from small molecules to peptides to proteins to antibodies to live cell-therapies. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
