Amgen

Amgen Tampa, FL, USA
Apr 03, 2020
Full time
At Amgen, our mission is simple: to serve patients. To support that mission, Amgen is seeking a Sr. Manager Information Systems to lead the Integrated Business Planning team within the Operations IS (OIS) group to support the Global Commercial Supply Chain business organization. The Sr. Manager IS will report to the Head of IS for Global Commercial Supply Chain and will primarily be responsible leading the implementation of the Integrated Business Planning strategy. Key responsibilities of this role include: Own and support planning software and strategic roadmap of Integrated Business Planning Capabilities for Global Supply Chain (i.e. Technological capability for Inventory Planning, Capacity Planning, Dashboard and analytics) Lead as a technology authority in the development and improvement of platform solution to meet the growing need of planning processes Act as IS owner and representative of the planning software, an essential business and IS partnership in driving forward planning capabilities Work with onshore/offshore Anaplan model builders for system capabilities, improvements and support to meet the needs of the Integrated Business Planning process. Lead technical development and partnership with the external consulting teams Develop roadmap for capabilities of Global Supply Chain planning processes Develop approach and align business requirements along solutions life-cycle Work with and educate key partners in the organization, including Operations, Finance and Commercial, to design the most effective planning process Develop new capabilities, new functionality, provide post-implementation user support, design a sustainment model and build improvements Responsibilities also include: Standardize & automate activities using the platform solutions (i.e. Anaplan, SAP, Tableau etc) Communicate and collaborate with diverse key partners including Global supply chain, Operations, Finance and Commercial to identify business requirements and provide experienced guidance on the best approaches to build efficient models Prepare and communicate regular project updates to key partners including senior management. Work with Global Supply Chain, Finance and Commercial to ensure the integrity of the data flows to and from internal systems Basic Qualifications: Doctorate degree plus 2 years of Information Systems experience Or Master's degree plus 6 years of Information Systems experience Or Bachelor's degree plus 8 years of Information Systems experience Or Associate's degree plus 10 years of Information Systems experience Or High school diploma / GED plus 12 years of Information Systems experience Preferred Qualifications: 2 + years of experience crafting, modeling and deploying models with widely used planning and analytics applications such as Anaplan, Hyperion, SAP, Tableau etc Familiarity in working using Agile methodology for software development Self-starter with high attention to detail, able to work independently Familiarity with AWS, EDL, BOM structure and working with large data structures Good communications skills with all levels of an organization (written and oral) Good understanding of finance, sales operations and supply chain Experience in working in and between business/finance operations and IT Ability to translate complex information into comprehensive, concise and high-quality business requirements that resonate with partners Excellent project management skills and ability to effectively balance multiple ongoing projects to meet deadlines 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. 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.
Amgen West Greenwich, RI 02817, USA
Apr 02, 2020
Full time
Amgen is seeking a Maintenance Technician at its West Greenwich, RI campus to join the Facilities & Engineering Utilities Maintenance organization! The position will report to the Maintenance Manager. The Maintenance Technician is responsible for performing installation, troubleshooting, maintenance, repair, testing, and documentation/logs of a wide variety of HVAC, utility, and facility equipment used in manufacturing, utility plants, analytical labs, and office areas in addition to completing various quality system and safety documentation. All work to be completed in a safe and timely manner according to planning and predefined schedules while following Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOP), and Amgen regulations. The Facility & Engineering Utilities Maintenance department is a highly skilled work force delivering responsive, high quality, cost effective service. We create a competitive advantage for the organization's core business through engineering, maintenance, and right the first-time execution. This is an administrative shift Monday-Friday (typically normal business hours). Responsibilities Perform operations, maintenance, and trouble-shooting of site HVAC & Utility equipment - including chillers, coldrooms, standalone refrigerators/freezers Interact with peers and clients in manufacturing, maintenance, utility plant, analytical labs and contracted services Understand and follow all Energy Control / LOTO (Lock out Tag out) procedures and able to execute LOTO of utility systems and equipment Read and understand equipment drawings, schematics, and technical manuals Possess an understanding of process control systems related to site utilities Performs other duties assigned Basic Qualifications Associate's degree and 2 years of Maintenance experience Or 2 years in a technical school setting with hands-on experience Or High school diploma / GED and 4 years of Maintenance experience Preferred Qualifications Rhode Island Refrigeration License 2 year technical/AA/AS degree in building maintenance, mechanical maintenance, plant engineering 5+ years in an FDA (GMP) or similar regulated environment Experience with installation, troubleshooting, maintenance, repair and testing of HVAC, laboratory and utilities equipment Intermediate knowledge of pneumatic, mechanical, and hydraulic fundamentals as well as intermediate skills in the use of power and hand tools in the building trades such as carpentry, plumbing, and electrical Effective oral and written communication skills Intermediate computer and typing skills Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do. We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions. Amgen focuses on areas of high unmet medical need and uses 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 an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. 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.
Amgen Thousand Oaks, CA, USA
Apr 02, 2020
Full time
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. 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. If you are a highly motivated and team-focused process development scientist seeking a new opportunity, the Synthetics Enabling Technologies (SET) group, part of Amgen's Pre-Pivotal Drug Product Technologies organization is hiring. Come join us! This role is based in Thousand Oaks, CA. The SET group serves as a key collaboration with the partners in Process Development and Research & Discovery. The group's main responsibilities include: Solid state form selection and characterization support for DS and DP process development for small molecules and biologics programs. Generation of fundamental knowledge to establish form development strategies and Target Product Profile. Small molecule developability assessment and pre-clinical formulation development. Biopharmaceutical property evaluations utilizing in silico and in vitro models to guide development path. Early clinical support for small molecule liquid dosage forms (e.g., drug-in-bottle, parenteral) and technical transfers to support clinical manufacturing process. In this role, the scientist will play a proactive role in the solid-state form evaluation and characterization, and the application of innovative materials science approaches, to guide the DS and DP development. Responsibilities will include: Designing and conducting screening and crystallization experiments of small molecule drug candidates (including salts, co-crystals, hydrates, solvates and polymorphs). Evaluating and recommending suitable solid-state drug substance forms, identifying any gaps/risks associated with process development, and providing mitigation strategies to the preclinical and early formulation development teams. Performing a range of solid state characterization of pharmaceutical materials, including particle characterization (e.g., particle size & shape, surface area), X-ray diffraction, thermal analysis and spectroscopy. Assessing structure-property relationships of APIs and providing material options with the desired physicochemical properties for DS/DP development. Building and maintaining strong working relationships with internal and external partners. Supporting departmental activities including training staff and presenting scientific results at internal/external meetings. Contributing to regulatory and intellectual property filings. Keeping apprised of new technologies in pharmaceutical materials science and collaborating with external partners. Basic Qualifications: Doctorate or Doctorate degree completed by Dec 2019 OR Master's degree & 4 years of scientific experience OR Bachelor's degree & 6 years of scientific experience Preferred Qualifications: Doctorate Degree in one of the following areas: Materials Science, Chemical Engineering, Organic Chemistry, Physical Chemistry, Pharmaceutical Science, or a related scientific field with 2-4 years of post-doctoral or industry experience. Demonstrated, hands-on experience and expertise in designing and executing form screening and crystallization experiments to assess polymorphism, salt/co-crystal formation and solvate/hydrate formation. In-depth experience and proficiency in solid-state techniques (DSC, TGA, XRD, microscopy, DVS, particle characterization, Raman, IR, etc.). Good understanding in computational crystallography and data science to predict the properties and performance of drug substances/drug products. Working knowledge in preformulation and biopharmaceutics concepts to evaluate the developability of small molecule drug candidates. Demonstrated, successful track record of peer-reviewed journal publications and presentations. Excellent written, verbal, and presentation skills: ability to distill, develop, and present key messages relative to diverse audience requirements. Creative problem solver with proactive attitude and independence to collaborate and work within a cross-functional and multidisciplinary environment. We understand to successfully sustain and grow as a global enterprise and deliver for patients - we must ensure a diverse and inclusive work environment. 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. 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.
Amgen Thousand Oaks, CA, USA
Apr 02, 2020
Full time
This position reports into the Package Engineering group under FPT (Final Product Technologies) in Thousand Oaks, California. This position will apply engineering principles to execute the proper design, qualification and implementation of Primary and Secondary Packaging components and the associated systems such as documentation, equipment and processes. The position entails interpersonal, project management, technical problem solving and communication (written and verbal) skills, and the opportunity to work in teams and adapt to rapidly changing environment. Responsibilities: Support for testing and evaluation leading to recommendation and selection of primary and secondary packaging materials for both large and small molecule products Familiar with distribution testing per ASTM D4169. Familiarity with ASTM, ISO, TAPPI, USP and EP testing standards. Writing of test protocols, perform technical evaluations and testing to support reports used to justify the use of selected materials and packaging components. Writing Technical Specifications and Bill of Materials Build, modify, and approve engineering drawings utilizing Illustrator, Solid Works or similar software application. Support line trials and packaging validation activities prior to introduction of any new or change in components/processes Collaborate with cross-functional teams (i.e. Research, QA/QC, Supply Chain, Maintenance, Manufacturing, Regulatory, etc.) in pre-commercial and commercial activities. Basic Qualifications: Master's degree OR Bachelor's degree and 2 years of engineering/scientific experience OR Associate's degree and 6 years of engineering/scientific experience Or High school diploma / GED and 8 years of engineering/scientific experience Preferred Qualifications: BS Packaging, Mechanical Engineering, Chemical Engineering or Life Sciences 3+ years general packaging/engineering experience is strongly preferred Knowledge of primary and secondary packaging systems and material science is essential to the position. The position requires organizational, project management, technical problem solving and communication (written and verbal) skills, and the ability to work in teams and adapt to rapidly changing environment. Independent problem solver with demonstrated skills working in teams or leading project teams Strong Interpersonal and communication skills Passion and drive to develop and maintain a culture that is focused on continuous improvement, safety and actively participates in a teamwork environment that maintains a high performance culture 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. 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. 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.
Amgen Tampa, FL, USA
Apr 02, 2020
Full time
Amgen is seeking an Associate Systems Analyst - SAP Security to join the Enterprise Platforms Corporate Functions - Global ERP team based at the Amgen Capability Center in Tampa, Florida. The incumbent will be responsible for project activities, including solution design, build, testing, and implementation. In addition, the successful applicant will be required to collaborate with development, basis and functional team members to deliver, operate and continuously drive fundamental technology improvements in GERP platform by working closely with Architects, AMS support teams to efficiently deliver Amgen's Global ERP solutions in a 24X7 regulated environment. At Amgen, our mission is simple: to serve patients. Our new Tampa Capability Center provides essential services that enable us to better pursue this mission. This state-of-the-art center serves as a base for finance, information systems, and human resources professionals to make a significant impact at one of the world's leading biotechnology companies. By centralizing these services and activities, we can improve teamwork, share standard methodologies, innovate and streamline processes for our entire enterprise. The invaluable contributions of our hardworking Tampa team will help us develop the vital and innovative medicines that treat serious illness and unmet medical needs around the globe. Key Responsibilities: Participate in requirement gathering, assessment, design, development, testing, implementation and support of SAP Security roles, across all SAP landscapes. Research new solutions to meet current and future security requirements. Implement continuous improvement of Amgen's Global SAP Security design, processes and procedures. Solve security issues for GERP platform that includes SAP ECC, GRC, BI, ATTP, GTS, SolMan, HANA, Fiori and PO. Follow Amgen security policies, processes, and procedures across all SAP systems. Assist with configuration activities performed on GRC Access Control module. Provide support for SAP Security audits and compliance requests. Provide support for SAP License Audit. Basic Qualifications: Bachelor's degree and 2 years of Information Systems experience Or Associate degree and 6 years of Information Systems experience Or High school diploma / GED and 8 years of Information Systems experience Preferred Qualifications: 3+ years of SAP security experience, including at least 1+ years of GRC Access Control experience. Knowledge of ERP security concepts, including design standards and appropriate methodologies. Good understanding of the SAP Security authorization concept across SAP components. Experience/Knowledge in Segregation of duties, Mitigation Controls etc. Ability to take direction well, always follow the process and procedures. Able to work in teams to complete tasks. Good written, verbal communication, and presentation skills. Positive attitude and a good work ethic. Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering creative 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. Amgen focuses on areas of high unmet medical need and uses 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. Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do. We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. 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.
Amgen West Greenwich, RI 02817, USA
Apr 01, 2020
Full time
We are looking for a Senior Associate Environment, Health, Safety and Sustainability Manager (EHSS) to help drive outstanding performance in a diverse and rapidly growing manufacturing environment! Under the direction of the Director (EHSS), the successful candidate will have responsibility for supporting various requirements outlined in site EHSS programs. As a core member of the team, the candidate will be encouraged to interact frequently with internal clients, be proactive, and be directly engaged in the operations of the facility. Responsible to implement, manage, and monitor aspects of facility safety and environmental compliance programs at the site level and manage competing priorities on a routine basis. This role will have broad responsibilities across the safety and environmental compliance disciplines. Responsibilities include: Assist in the interpretation of EHSS regulations to ensure compliance with Corporate, Federal, State and local requirements; Develop and implement environmental compliance plans for programs such as air quality, storm water, wastewater treatment, hazardous waste management, pollution prevention, or solid waste management; Support and/or direct aspects of the site Environmental Sustainability program; Perform EHS inspections throughout the facility (lab, manufacturing, construction); Conduct internal reviews and audits to ensure that safety and environmental procedures are being followed; Perform job hazard analysis and support Industrial hygiene, ergonomic, and other safety assessments as needed; Participate in emergency response activities and be a member of the emergency on call team on a rotating basis; Conduct and coordinate formal and informal environmental training for staff and contractors; Support EHS reviews of new material acquisitions; Maintain appropriate records and documentation; Identify and assist in implementing EHS program improvement initiatives; Partner with all levels of internal client and site/corporate EHS organizations; Act as an EHS representative for internal client organizations; Assist in Accident/Incident investigations and Root Cause Analysis. Basic Qualifications: Master's degree OR Bachelor's degree and 2 years of EHSS or corporate services experience OR Associate's degree and 6 years of EHSS or corporate services experience OR High school diploma / GED and 8 years of EHSS or corporate services experience Preferred Qualifications: BS degree in environmental, safety, technical, scientific or engineering fields. 6 + years of experience developing/supporting EHS programs within industry. Possess one or more professional credentials (CIH, CSP, ASP, CHMM, EIT). Previous experience working within the biotechnology sector, preferably in a cGMP environment. Amgen focuses on areas of high unmet medical need and uses 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. Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do. We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. 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.
Amgen Cambridge, MA, USA
Apr 01, 2020
Full time
Amgen is seeking a Quality Complaints Sr. Associate to triage all complaints and own L1 Records, supporting the Product Complaints and Surveillance Team. The Product Complaints and Surveillance team owns and executes the end-to-end global complaint process and management systems, ensuring appropriate business connection across Amgen. In doing so, the focus is on assuring complaint processes and systems remain fully compliant through the quality operating standards and procedures to current, emerging internal and external requirements. In addition, the team translates information from the market to drive continuous improvement. The Sr. Associate conducts low to medium complexity complaint investigations and determines if complaint investigations require escalation for further investigation. The Sr. Associate Quality Complaints will be responsible for triaging complaints and managing L1 records for 1st Shift (Sunday through Thursday or Tuesday through Sunday 8am - 5pm). Key Responsibilities: Triage product complaint records Ensures quality of complaint records Applies analytical skills to evaluate complex situations using multiple sources of information Executes SOP requirements Develops solutions to technical problems of moderate complexity Screens, evaluates, reports and resolves record integrity issues Must be able to work off-shift Basic Qualifications Master's degree OR Bachelor's degree and 2 years of Quality experience OR Associate's degree and 6 years of Quality experience OR High school diploma / GED and 8 years of Quality experience Preferred Qualifications Quality and manufacturing experience in biotech or pharmaceutical industry Bachelor's Degree in a Science Field Ability to successfully manage workload to timelines Familiarity with basic project management tools Demonstrated ability to consistently deliver on-time, and high-quality results Ability to operate in a matrixed or team environment Understanding of the applicable manufacturing/testing processes (i.e. API, Drug Substance, Drug Product, Packaging, Device manufacturing processes) 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. 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 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. 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.
Amgen Thousand Oaks, CA, USA
Apr 01, 2020
Full time
Amgen is seeking a Business Performance Senior Manager (BPSM) at its headquarters in Thousand Oaks, CA to join the Global Regulatory Affairs and Safety (GRAAS) organization. This individual will report to the Director of the GRAAS Strategic Planning & Operations and will be responsible for creating, maintaining and advancing workforce strategy. The BPSM will be a key part of the GRAAS Strategic Planning & Operations (GRAAS SPO) team, supporting GRAAS by developing and executing a workforce strategy that ensures each team is appropriately resourced given the projected demand for that teams' services. This role will interface regularly with senior leadership in GRAAS, as well as partner functions around the company. The successful candidate will be proactive, a strong problem-solver, able to handle and understand large sets of data, and willing to apply their knowledge in practical and creative ways. GRAAS is responsible for assessing and communicating the benefit/risk profile of Amgen's pipeline and marketed products, owning the regulatory relationship with worldwide health authorities, and guiding the registration of Amgen's products in the markets we serve. It's nearly 900 staff members operate in 40+ countries around the world, and interact daily with hundreds of vendors, contractors, and outsourced workers. Responsibilities of this role include: Developing and maintaining a GRAAS resource demand model Proactively establishing relationships with GRAAS's customers and partners to predict potential changes to resource demand Partnering with GRAAS leadership to identify opportunities to shift resourcing between internal, external, and contract staff to deliver higher quality, lower cost, increased capacity, or fill capability gaps Working with HR and University Relations to create a recruiting and onboarding program to meet GRAAS's predicted resource needs into the future Partnering with GRAAS leadership to understand changes in organization and strategy that may impact resourcing needs Owning and maintaining the GRAAS Resourcing Strategy and promoting its adoption Tracking current GRAAS resourcing and reporting its status to GRAAS leadership Serving as GRAAS's primary point of contact with the R&D Supplier Performance Management team Supporting efforts to engage GRAAS staff around the world Basic Qualifications Doctorate degree and 2 years of resource modeling experience OR Master's degree and 6 years of resource modeling experience OR Bachelor's degree and 8 years of resource modeling experience OR Associates degree and 10 years of resource modeling experience OR High school diploma / GED and 12 years of resource modeling experience Preferred Qualifications Advanced MS Excel experience MS Word / PowerPoint experience Smartsheet experience Tableau experience Resource modeling and forecasting experience Strong verbal and written communication skills 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.
Amgen Thousand Oaks, CA, USA
Apr 01, 2020
Full time
Motivated by a passion for developing creative solutions to help teams access knowledge that can inform key decisions throughout the drug development life cycle, Amgen's Center for Design and Analysis has recently established a Knowledge Management (KM) team. Partnering with a team of data scientists, the KM team identifies opportunities to use data and technology alongside an understanding of business processes and human/interpersonal factors. Our solutions connect people to the stories, experiences and other people, equipping them to ask better questions, of the right people, more quickly. Our new Senior Associate will deliver solutions that focus on the end user experience through Taxonomy development, assessing and curating data sources and providing metrics. Specific responsibilities will include: Managing the execution of the Knowledge Management implementation plan with a focus on the needs of Clinical Development and providing value to partners in other functions such as Regulatory and Commercialization. Coordinating the ongoing maturation of supporting technologies that enables KM. Driving the creation and curation of knowledge assets. Supporting the communication and implementation of knowledge management solutions/change management approaches across people, process and technology. Delivering internal training, education and consulting on KM concepts and methodologies. Basic Qualifications Master's degree OR Bachelor's degree and 2 years of knowledge management related experience OR Associate's degree and 6 years of knowledge management related experience OR High school diploma / GED and 8 years of knowledge management related experience Preferred Qualifications Master's Degree related to knowledge or technical management or Bachelor's Degree and 2 years related experience. Experience in knowledge management development utilizing taxonomy and ontology concepts and approaches. Excellent communication, organizational and presentation skills including the ability to work with diverse cross-functional teams. 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.
Amgen Cambridge, MA, USA
Apr 01, 2020
Full time
Amgen is seeking a Process Development (PD) Senior Associate to support all aspects of small molecule process development to advance the Amgen pipeline as part of the Pivotal and Commercial Synthetics organization. The PD Senior Associate will work under the supervision of a Ph.D. Scientist, partner with drug substance development teams and be expected to develop innovative solutions to prepare small molecule drug candidates. Research activities will include reaction development, characterization of reaction profiles and isolated compounds, process scale-up development, and participating in cGMP campaigns targeting bulk Active Pharmaceutical Ingredient in support of clinical supply and commercial process development activities. The PD Senior Associate will maintain electronic laboratory notebooks and computer files, participate in group and project meetings, and attend seminars. The PD Senior Associate will work in a team environment, collaborating with various colleagues in process development and engage in technical transfer activities with Amgen's global partners. Basic Qualifications: Master's degree or Master's degree completed by July 2020 OR Bachelor's degree and 2 years of Scientific, Process Development or Operations experience Preferred Qualifications: Master's degree in Organic Chemistry or related field Experience in the pharmaceutical, biotech, or other related industry Broad knowledge of organic chemistry reactions and current scientific literature Basic laboratory skills including synthesis, purification, and characterization of organic small molecules Experience with analytical techniques including NMR, HPLC and Mass Spectrometry Experience in reviewing and interpreting analytical data Demonstrated ability to work in a fast-paced team environment Excellent presentation, written and verbal skills 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.
Amgen South San Francisco, CA, USA
Apr 01, 2020
Full time
The Amgen Postdoctoral program is committed to providing future scientists with an enriching environment to inspire innovation that will contribute to the development of human therapeutics! The Pharmacokinetics and Drug Metabolism department is seeking a highly motivated postdoctoral candidate to develop mechanistic data-driven pharmacology models for therapeutics with complex mechanisms of action including siRNA and PROTACs. The models will be used to guide assay development for in vitro-in vivo correlations, advance understanding of ADME properties, and establish PK-PD relationships across a range of pre-clinical species to guide first in human dose selection. The successful applicant will perform independent research within the context of a highly collaborative environment and will split their time between model development in R, and designing, executing and analyzing in vitro and in vivo experiments for model validation and advancement. The postdoctoral position is for 3 years. Role Responsibilities: Planning and execution of molecular, cellular and sample analysis from in vivo studies to enable quantification of essential model parameters. Responsible for generating reproducible and well-controlled datasets suitable for publication in leading peer-reviewed journals. Construction of in vitro and in vivo pharmacology models to predict duration, efficacy and PK-PD relationships for oligonucleotide therapeutics and PROTACs. Responsible for performing comprehensive model validation. Developing deep expertise in the siRNA and PROTAC therapeutic platforms Collaborating with teams across medicinal chemistry, therapeutic discovery, bioanalytics, and in vivo pharmacology to utilize models where applicable to support pipeline projects. Contribute innovation, ideas, and literature insights into the implementation of pharmacology modeling in the drug discovery and translation workflow. Under the guidance of a mentor, build a cohesive, achievable course of study that can be compiled into manuscripts for publication in peer-reviewed journals and presentation in scientific forums. Basic Qualifications PhD at the time of appointment. Preferred Qualifications PhD in Pharmacology, Biophysics, Biomedical Engineering, Biochemistry, or Molecular/Cellular Biology Expertise in mechanistic modeling using R or related software, biophysical techniques including SPR, enzyme kinetics, biochemical and cellular assay development, and/or mechanistic cellular biochemistry Record of independent critical thinking and the ability to design, execute, and interpret experiments, as exemplified by publications Highly proficient with statistics, figure design, and scientific data analysis software (e.g., Graphpad Prism, Image J, Origin, and R) Desired Qualifications Expertise in the ubiquitin-proteasome system, cellular protein homestasis, PROTACs, and/or RNAi 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. Amgen will consider for employment qualified applicants with criminal histories in a manner consistent with the San Francisco Fair Chance Ordinance.
Amgen Thousand Oaks, CA, USA
Apr 01, 2020
Full time
Amgen is seeking a Compliance Senior Manager based in our global HQ in Thousand Oaks, CA who will report into the Compliance Director. As a member of the Policies, Training, Communications & Business Ethics (PTC&BE) group, the Compliance Senior Manager is responsible for Global Healthcare Compliance policy development. The Senior Manager will also provide policy advice to critical initiatives and programmatic improvements to the Global Healthcare Compliance program. Amgen's Worldwide Compliance and Business Ethics department (WC&BE) consists of a highly qualified and motivated team of professionals who identify, review, evaluate, handle and advise on compliance considerations within the organization. Key Responsibilities for the Compliance Senior Manager include: Based on input from subject matter authorities, develops and updates global Healthcare Compliance controlled documents, including global corporate compliance policies Demonstrates knowledge of global corporate compliance policies to support development of written Code of Conduct, annual Code of Conduct training, and other training initiatives Supports business development opportunities from a compliance perspective, including reviewing compliance-related contract terms and conducting compliance due diligence of specified business development opportunities Prepares written communications intended for multiple internal stakeholder audiences Develops and handles project schedules and processes to ensure the project timelines/deadlines are met Coordinates project team meetings and work in cross-functional teams to ensure execution of initiatives Assists in management of the execution of global Healthcare Compliance policy and training plans Provides strategic input into the processes across WC&BE related to the execution of the global Healthcare Compliance program Maintains knowledge of the healthcare industry, recent federal and state enforcement activities, and the laws and regulations (including the federal and state anti-kickback laws) relating to the development, approval, and commercialization of biopharmaceutical products Maintains relationships with consultants and attorneys Represents WC&BE on corporate cross-functional committees Works closely with internal Global Healthcare Compliance Operations to ensure effective implementation of compliance procedures and processes Basic Qualifications: Doctorate degree and 2 years of Compliance and/or Law and/or Regulatory experience Or Master's degree and 4 years of Compliance and/or Law and/or Regulatory experience Or Bachelor's degree and 6 years of Compliance and/or Law and/or Regulatory experience Or Associate's degree and 10 years of Compliance and/or Law and/or Regulatory experience Or High school diploma / GED and 12 years of Compliance and/or Law and/or Regulatory Preferred Qualifications: Proficiency in the area of policy and SOP writing Knowledge of the healthcare industry, recent federal and state enforcement activities, and the laws and regulations relating to the development, approval, and commercialization of biotechnology/pharmaceutical products Confirmed project management ability Strong attention to detail, organization skills, and the ability to work independently, efficiently, and with minimal supervision Effective communication, writing and presentation skills Proficient in Word, PowerPoint, Outlook and document management systems Ability to handle ambiguity and complex situations Strong ability to synthesize vast amounts of complex data, and clearly and concisely articulate the relevant points at the right altitude Ability to think strategically and to translate strategy into action plans Ability to prioritize, be proactive, resolve conflicts, meet deadlines, and be a great teammate Ability to work with all levels of staff and management, and establish links across subject areas Experience in building balanced working relationships across departments, making difficult decisions, solving problems, working under time constraints, addressing internal peers and external clients, handling numerous projects at once 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. 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. 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.
Amgen Thousand Oaks, CA, USA
Apr 01, 2020
Full time
Amgen's Research and Development (R&D) Business Operations organization addresses complex business challenges with exceptional people, tools and processes. The team delivers on key initiatives and provides tactical support to ensure R&D scientists and staff receive the goods and services they require, strong analytic support for spend and management of external partners through robust supplier oversight and governance programs. The Senior Manager, R&D Business Operations supports the Development Organization including Medical, Therapeutic Areas and the Centers for Observational Research and Design and Analysis. As a leader, they guide a team committed to exceeding productivity and operational goals on a global basis. The Senior Manager will assist in developing supplier and expense management strategies, ensure efficient execution of these strategies and find opportunities to align, improve and re-design processes and tools. In addition, they will participate or lead R&D-wide strategic initiatives to improve operational efficiency and enable the organizational vision to be achieved. As a creative problem solver who can deliver meaningful results, this role will focus on: Leading a team of supplier performance managers. Developing strong collaborative relationships with internal partners to support and proactively respond to business needs. Advocating for internal partners through engaging with global corporate functions to remove barriers and develop solutions to evolving business needs. Developing outstanding supplier performance management and supplier governance strategies to ensure smooth execution of contracted deliverables. Partnering with Supplier Governance to explore alignments in supplier oversight and find innovative solutions that elevate the strategic values of supplier relationships. Collaborating with Global Strategic Sourcing to support R&D wide sourcing and productivity initiatives. Establishing fit for purpose expense management strategies to support planning, tracking and reporting. Partnering with Finance to ensure holistic expense management and provide insights. Ensuring adherence to corporate procurement guidelines and coordinating end to end source to pay processes. Basic Qualifications Doctorate degree and 2 years of biotech/pharma-related business operations/supplier management experience OR Master's degree and 6 years of biotech/pharma-related business operations/supplier management experience OR Bachelor's degree and 8 years of biotech/pharma-related business operations/supplier management experience OR Associate's degree and 10 years of biotech/pharma-related business operations/supplier management experience OR High school diploma / GED and 12 years of biotech/pharma-related business operations/supplier management experience AND 2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources Preferred Qualifications Degree in biology, life sciences, health, medical or clinical sciences along with additional education in finance or business. Strong background in mid- and late-stage drug development that includes familiarity with multiple therapeutic areas, regulatory operations, observational studies, biostatistics and medical operations. Experienced "integrator" role across multiple organizations, teams and processes with proven ability to advance strategic imperatives. Familiarity with clinical development compliance requirements such as GCP, GPVP and ICH. Familiarity with procurement compliance requirements (Sunshine Act, SOX, HCC). Familiarity with multiple sourcing models (Fee-for-service, dedicated resource, functional service provider). Finance and budget management experience including cost analysis and reporting. Proven ability as people leader who can translate strategies into actionable goals and cultivate a team sense of purpose. Proven experience as a change agent and managing through organizational transformation. Exceptional interpersonal, organizational, critical thinking and verbal/written communication skills. Proven ability to develop collaborative internal and external relationships and navigating matrixed organizations. Being able to adapt work and communication styles to meet organization needs. Strong planning and project management skills with the demonstrated ability to work effectively in a fast-paced environment with multiple high priority projects. Experience with analytics software (Microsoft Access, SPSS, Spotfire, Tableau, Smartsheet), document management applications, portfolio planning tools and financial systems (Planisware, Veeva, SAP). 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.
Amgen Thousand Oaks, CA, USA
Mar 31, 2020
Full time
Job Summary Amgen is looking for a Sr. Manager, Digital Media to be part of the Marketing Operations & Innovation Team. The Sr. Manager is responsible for leading, planning and developing new media & digital capabilities and partnerships for Amgen. He or she will be a key driver of our audience first, engagement driven media strategy, partnerships and tactical execution, and plays a pivotal role in crafting and implementing a vision of what digital media will look like for US Business Operations and marketing teams. This person will be savvy in digital and new, innovative media opportunities. Ability to be able to translate data and insights to help realize moments of receptivity across the customer journey ensuring our media efforts align the right brand message to the right channel at the right time. The Sr. Manager will be part of a robust marketing excellence team who frequently interacts with cross-functional teams and partnering agencies/vendors to connect consumer and healthcare professional marketing activities & media performance data across brands, business strategy, goals and tactics. This position reports to the Director of Marketing Operations & Innovation. Job responsibilities include: Develop & Elevate Amgen's Marketing Capabilities and Standardize Strategic Approach: Develop, execute and standardize Amgen's approach to digital media, partnerships and execution to meet brand objectives and stimulate appropriate consumer awareness, new patient starts, and adherence. Serve as a sponsor for media innovation. Make the business case and demonstrate how new and existing digital capabilities could positively impact existing business processes. Develop seamless omni-channel user experience with emphasis on context. Work with brand teams to understand their customers, the content they are consuming, where they're coming from and their goals and challenges. Overall responsibility to ensure the voice of customers and patient needs are being considered in choice of media channels. Ensure messaging is consistent across channels and that content ties engagement channels together. Drive Digital Execution Serve as subject matter expert across Paid Social & Display channels, running the day-to-day and leading agency counterparts. Lead learning agendas for Paid Social & Display, inclusive of measuring, optimizing, and disseminating findings to the broader organization. Partner to develop digital media journeys, channel-right creative, and audience strategies to deliver highly targeted, premium, and relevant media programs. Elevate digital marketing capabilities surrounding SEO, SEM, PPC, Ad Servers, Programmatic Buying Platforms, Online Video, Email Marketing, Push notifications, Mobile and more. Lead the Measurement & Optimization Plan: Partner with internal brand and data science teams, as well as external vendors/agencies, to identify / build a media measurement framework and communication cadence. Develop key metrics and corresponding benchmarks to assess value through analytics, measure success, and recommend campaign optimization based on results. Use analytics and research to provide recommendations to brand teams on channel selection and channel mix. Dive deep into weekly campaign performance, use data to understand trends, identify successes and optimization opportunities, as well as forecast future channel performance. Work in Teams: Collaborate, drive internal partner alignment, engagement and develop positive relationships with cross-functional teams and agency partners to ensure effective and productive promotional capabilities. Develop and champion an environment of standard methodology sharing and standardization across brands and customer audiences (DTC & HCP). Acts as subject matter expert practices for digital marketing capabilities and execution; advises cross-functional teams on process and technical execution. Works with broader Operations and cross-functional teams to develop, optimize, document, and socialize campaign and channel execution strategies. Project Management Manage project budgets and closely monitor performance, ensuring efficient delivery of all programs. Understand and align brand needs and objectives with timely strategic media solutions. Coordinate the development of end to end digital media plans, work with brands to refine their briefs and media agencies to ensure flawless execution. Push brand partners to elevate work and thinking beyond "the typical," be the bridge between strong, conceptual thinking, and data-driven, analytical approaches to problem-solving. Travel as needed for agency collaboration (~10%). B asic Qualifications Doctorate degree and 2 years in a strategic marketing, planning, media/communication strategy role in a customer facing industry OR Master's degree and 4 years in a strategic marketing, planning, media/communication strategy role in a customer facing industry OR Bachelor's degree and 6 years in a strategic marketing, planning, media/communication strategy role in a customer facing industry OR Associate's degree and 10 years in a strategic marketing, planning, media/communication strategy role in a customer facing industry OR High school diploma / GED and 12 years in a strategic marketing, planning, media/communication strategy role in a customer facing industry Preferred Qualifications 10+ Years of work experience in Digital Media with an emphasis on Growth & Performance Master's degree (MBA, MSc, etc.) a plus In-depth experience with Google Marketing Platform (Google DV360 and DCM), Facebook Business Manager, Facebook Ads Manager, Snapchat, Pinterest, YouTube, Twitter, and more Excellent verbal and written communication skills; includes strong interpersonal skills with demonstrated ability to work effectively Experience in Pharmaceutical Consumer Marketing and/or Consumer Package Goods marketing industry Experience managing and working with outside vendors / advertising agencies Self-starter with an innate curiosity and the commitment to test, learn, adapt and be agile in a constantly evolving environment Experience managing and optimizing digital marketing campaigns and channels to deliver against acquisition and retention performance indicators Strong understanding of the rapidly evolving digital media landscape You are an authority in Paid Social & Display media (including underlying technology - and the unique role these two channels plays among a full marketing mix) and how to use these channels to drive direct-to-patient messaging, acquisition and retention You are able to think holistically and have a deep understanding of our consumers, their digital media habits You are also eager to innovate, measure, test, sometimes fail, learn, and evolve to shape the strategy and planning for unbranded/branded campaigns across Paid Social & Display media 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. 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 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. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. 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.
Amgen Santa Rosa, CA, USA
Mar 31, 2020
Full time
Territory: R65D04 - Santa Rosa, CA (Red Team) Covering: Santa Rosa, CA No relocation assistance provided for this position. Amgen's medicines treat serious illnesses and our research address diseases with a limited number of treatment options. With a robust and differentiated pipeline, Amgen remains committed to advancing science to dramatically improve people's lives. As a values-based organization with a powerful sense of shared purpose toward our mission: to serve patients, we are actively searching for a Senior Specialty Representative to deliver on this commitment to patients. Amgen supports and encourages our team members to have long term, fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities such as this opportunity to craft a long-term career with Amgen. The Senior Specialty Representative acts as the primary customer contact and is responsible for executing marketing strategy and promoting Amgen products as led by the District Manager. Our Senior Specialty Representatives achieve territory sales by utilizing their background and experience to: Provide current and comprehensive clinical knowledge of Amgen's products and effectively communicate the clinical and economic benefits of the products to medical professionals Perform as a sales leader to achieve territory sales by executing and delivering branded sales messages strategies. This includes: delivering branded sales messages, executing planned programs, scheduling and following-up with medical educational programs, and achieving or exceeding sales targets Utilize internal and external relationships to service and manage accounts which includes: ensuring product access, resolving/triage reimbursement issues, and maintaining product contracts Analyze business effectiveness of sales activities and territory analysis, as well as develop territory plans with the District Manager Have passion for our products and sustain that passion through the entire sales cycle while always building our brand, never losing sight of how we serve patients Partner with other colleagues to share best practices and be in a state of continuous curiosity and learning to help grow as a Senior Specialty Representative Leverage passion for disease state awareness, industry, regulatory and competitive changes to deliver agreed results Basic Qualifications: Bachelor's Degree and 3 years of sales experience OR Associate degree and 6 years of sales experience OR High school diploma/GED and 8 years of sales experience Preferred Qualifications: Three or more years of sales experience within pharmaceutical, biotech or medical device industry Product or hospital sales experience in the areas of oncology, nephrology, dermatology, rheumatology, inflammation, cardiology, neurology, endocrinology, hepatology, gastroenterology or infectious diseases; and the diseases and treatments involved with these specialties Local market knowledge A Bachelor's degree in Life Sciences or Business Administration Adaptability with our Core Competencies: Planning and Organizing; Leveraging Business, Industry, and Technical Knowledge; Communicating with Impact; Driving for Results; and Cultivating Internal and External Relationships. Amgen is a Fortune 150 company operating in nearly 100 countries around the world. We invest in highly skilled, dedicated and collaborative individuals who are ready to contribute to our mission in meaningful ways and make a difference in the lives of our patients. 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.
Amgen Modesto, CA, USA
Mar 31, 2020
Full time
Territory: R65D03 - Modesto, CA (Red Team) Covering: Modesto, CA No relocation assistance provided for this position. Amgen's medicines treat serious illnesses and our research address diseases with a limited number of treatment options. With a robust and differentiated pipeline, Amgen remains committed to advancing science to dramatically improve people's lives. As a values-based organization with a powerful sense of shared purpose toward our mission: to serve patients, we are actively searching for a Senior Specialty Representative to deliver on this commitment to patients. Amgen supports and encourages our team members to have long term, fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities such as this opportunity to craft a long-term career with Amgen. The Senior Specialty Representative acts as the primary customer contact and is responsible for executing marketing strategy and promoting Amgen products as led by the District Manager. Our Senior Specialty Representatives achieve territory sales by utilizing their background and experience to: Provide current and comprehensive clinical knowledge of Amgen's products and effectively communicate the clinical and economic benefits of the products to medical professionals Perform as a sales leader to achieve territory sales by executing and delivering branded sales messages strategies. This includes: delivering branded sales messages, executing planned programs, scheduling and following-up with medical educational programs, and achieving or exceeding sales targets Utilize internal and external relationships to service and manage accounts which includes: ensuring product access, resolving/triage reimbursement issues, and maintaining product contracts Analyze business effectiveness of sales activities and territory analysis, as well as develop territory plans with the District Manager Have passion for our products and sustain that passion through the entire sales cycle while always building our brand, never losing sight of how we serve patients Partner with other colleagues to share best practices and be in a state of continuous curiosity and learning to help grow as a Senior Specialty Representative Leverage passion for disease state awareness, industry, regulatory and competitive changes to deliver agreed results Basic Qualifications: Bachelor's Degree and 3 years of sales experience OR Associate degree and 6 years of sales experience OR High school diploma/GED and 8 years of sales experience Preferred Qualifications: Three or more years of sales experience within pharmaceutical, biotech or medical device industry Product or hospital sales experience in the areas of oncology, nephrology, dermatology, rheumatology, inflammation, cardiology, neurology, endocrinology, hepatology, gastroenterology or infectious diseases; and the diseases and treatments involved with these specialties Local market knowledge A Bachelor's degree in Life Sciences or Business Administration Adaptability with our Core Competencies: Planning and Organizing; Leveraging Business, Industry, and Technical Knowledge; Communicating with Impact; Driving for Results; and Cultivating Internal and External Relationships. Amgen is a Fortune 150 company operating in nearly 100 countries around the world. We invest in highly skilled, dedicated and collaborative individuals who are ready to contribute to our mission in meaningful ways and make a difference in the lives of our patients. 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.
Amgen Newbury Park, Thousand Oaks, CA, USA
Mar 31, 2020
Full time
The Health Economics Senior Manager develops and leads a Global Health Economics (GHE) value-evidence strategy for either an Amgen pipeline asset or Marketed Product in the therapeutic areas of oncology, inflammation, neurology, nephrology, bone or cardiology. Responsibilities include: 1. Integrates with a global research team and program to support the asset, as well as with individual regional and local business units, in alignment with the strategy, tracks and executes the GHE plan and delivers against goals. 2. Coordinates product and project activities. 3. Has budget responsibility and may immediately, or over time direct and develop staff. 4. Develops strategy and selection of Patient Reported Outcomes (PROs) for interventional trials and observational studies. Develops FDA briefing documents for PRO label discussions. 5. Develops core economic models with vendors or Amgen internal center of excellence. Works with Amgen international affiliates to adapt core economic models for regional use 6. Designs existing data studies, develops or approves research project plans, and oversees execution. 7. Develops and communicates the Global Value Dossier (GVD) and final value propositions and validates that the regional dossiers (e.g. AMCP Dossier) are consistent with the GVD. 8. Assists in the development, creation, and review of the US AMCP Dossier for relevant pipeline assets 9. Designs or approves GHE-related aspects such as statistical analysis plan (SAP) of observational studies and interventional trials and consults on study execution. 10. Develops and oversees/conducts relevant meta-analysis, PRO, systematic review, utility measurement or other outcomes research study as determined by product evidence generation plans/strategy 11. Helps design product evidence generation strategy and communicate plans to cross functions teams 12. Serves as the GHE representative for the Global Publication Team and coordinates with affiliates and Regional HE on publication plan 13. Prepares GHE publications for dissemination. 14. Develops or consults on global reimbursement strategy and value proposition for payers. 15. Selects and works with study vendors. Basic Qualifications: Doctorate Degree and 2 years of health economics and outcomes research experience OR Master's Degree and 6 years of health economics and outcomes research experience OR Bachelor's Degree and 8 years of health economics and outcomes research experience Preferred Qualifications: Masters or PhD in Health Economics, Outcomes Research, Health Services Research, Pharmacy Administration or related discipline, or PharmD with a post-doctoral fellowship in one of these areas 3+ years' experience in global outcomes research including dossier submissions for reimbursement. 3+ years' experience in PRO/HRQOL research including questionnaire design, evaluation, and/or analysis. 3+ years' experience developing pharmacoeconomic models. Experience working with consumers of outcomes information Knowledge of epidemiology, economics, psychometrics and medical writing Amgen provides a collaborative and creative culture in a company with a strong track record of innovation. Our culture encourages open dialogue and diverse views to land on the best solutions, and we help ensure our staff are equipped to excel today and tomorrow. Amgen is committed to unlocking the potential 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. 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. Global Health Economics contributes by ensuring patient and payer perspectives are incorporated into the value generated for these innovative biologics. The department is committed to developing comprehensive evidence packages across cost modeling, database analysis, and patient reported outcomes to achieve unparalleled health technology submissions. 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.
Amgen Newbury Park, Thousand Oaks, CA, USA
Mar 31, 2020
Full time
The US Medical Leader for Tezepelumab is responsible for the development and implementation of US Medical strategies, including US launch and lifecycle management. This role is responsible for: The development and execution of US product medical strategy, via the US Medical Plan, including launch support and lifecycle management, in collaboration with the Global Medical Leader, Product Team/Portfolio Governance and alignment with Global strategy Identification of scientific evidence gaps, development of US evidence generation strategy in coordination with the Global team Participating in engagement of external key stakeholders (often in partnership with other functions) Supports Medical input into label and regulatory interactions, in alignment and with deep understanding of global strategy and program clinical trial data Supports implementation of Medical governance for respective product, which includes: Safety and pharmacovigilance as a key and effective partner with GRAAS Clinical trial conduct US risk management/minimization in collaboration with GRAAS Subject matter appropriateness (medical/scientific) of external interactions (e.g. Copy review, multichannel, congresses, 1-1 interactions, etc.) Ensuring appropriate medical support of compliance Key Activities: Maximizes Amgen's value proposition of respective product(s) through management and delivery of all medical and scientific activities, including launch and lifecycle management, in alignment with Global strategy and Evidence Generation Team (EGT) Participates in development of US cross functional strategy and supports medical execution. Provides input into medical and scientific insight for incorporation into US product strategies, via the US Medical Plan, and provides insights into Global strategies, plans and tactics as a participant in the Commercialization process Ensures understanding and incorporation of patient perspectives in all activities Executes product-specific US evidence generation strategy, in alignment with EGT, and supports execution of data communication strategy Supports product-specific US clinical trial execution Medical / Scientific contribution to Value Dossiers, compendia and interactions with payers in collaboration with VA&P Medical input into label and regulatory interactions, in alignment and with deep understanding of global strategy and program clinical trial data May participate in speaking engagements that represent Amgen to external and internal bodies on medical and scientific issues related to relevant product(s) Participates in the review of investigator sponsored studies Supports or implements external Stakeholder Strategy Engagement strategy and execution with medical experts, professional societies, patient groups and other key stakeholders Participates in advocacy from a medical perspective in partnership with Commercial, Government Affairs and GRAAS policy Builds Amgen's reputation as a science-based and patient-focused reliable partner Ensures Medical Governance Ensures human subject safety for marketed product in cooperation and effective partnership with responsible functions (e.g., GRAAS, Global Development) May support US clinical trial conduct Participates with the MAC operating committee in the material reviews. Actively participates in US risk management/minimization in collaboration with GRAAS May decide subject matter appropriateness (medical/scientific) of external interactions (e.g. copy review, multichannel, congresses, 1-1 interactions, etc.) Ensures appropriate medical leadership of compliance; accountable for the conduct of medical activities according to all relevant compliance standards, regulations and SOPs; Role models appropriate and compliant behaviors and contributes to creating a climate of compliance adherence across the organization Basic Qualifications MD or DO degree from an accredited medical school AND 2 years of clinical research, basic science research, medical affairs or clinical development experience in inflammation Preferred Qualifications Accredited fellowship in Allergy and Immunology (board certified or board eligible) Demonstrated ability as a medical expert in a complex matrix environment Pharmaceutical product development, product lifecycle and commercialization process knowledge with understanding of other functions; including, but not limited to, Clinical Operations, Commercial, Safety, Regulatory, Value & Access, and Medical Affairs Experience in regional/local medical practice and healthcare ecosystems Skilled at engagement, scientific exchange with external medical community Clinical research experience Scientific publication experience (developing manuscripts and/or congress abstracts) In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale Familiarity with concepts of clinical research and clinical trial design, including biostatistics Sound scientific and clinical judgement Knowledge of Good Clinical Practices (GCP), region regulations and guidelines, and applicable international regulatory requirements Familiarity of local pharmaceutical industry and legal/health system environment Skilled at effectively presenting ideas and documenting complex medical/clinical concepts in both written and oral communication History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues Network of medical, clinical contacts in inflammation We understand that to successfully sustain and grow as a global enterprise and deliver for patients - we must ensure a diverse and inclusive work environment. 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. 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. #LI-POST MD01 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.
Amgen Albany, NY, USA
Mar 31, 2020
Full time
Territory: B1F001 - Albany, NY (Blue Team) Covering: Albany, NY No relocation assistance provided for this position. Amgen's medicines treat serious illnesses and our research address diseases with a limited number of treatment options. With a robust and differentiated pipeline, Amgen remains committed to advancing science to dramatically improve people's lives. As a values-based organization with a powerful sense of shared purpose toward our mission: to serve patients, we are actively searching for a Senior Specialty Representative to deliver on this commitment to patients. Amgen supports and encourages our team members to have long term, fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities such as this opportunity to craft a long-term career with Amgen. The Senior Specialty Representative acts as the primary customer contact and is responsible for executing marketing strategy and promoting Amgen products as led by the District Manager. Our Senior Specialty Representatives achieve territory sales by utilizing their background and experience to: Provide current and comprehensive clinical knowledge of Amgen's products and effectively communicate the clinical and economic benefits of the products to medical professionals Perform as a sales leader to achieve territory sales by executing and delivering branded sales messages strategies. This includes: delivering branded sales messages, executing planned programs, scheduling and following-up with medical educational programs, and achieving or exceeding sales targets Utilize internal and external relationships to service and manage accounts which includes: ensuring product access, resolving/triage reimbursement issues, and maintaining product contracts Analyze business effectiveness of sales activities and territory analysis, as well as develop territory plans with the District Manager Have passion for our products and sustain that passion through the entire sales cycle while always building our brand, never losing sight of how we serve patients Partner with other colleagues to share best practices and be in a state of continuous curiosity and learning to help grow as a Senior Specialty Representative Leverage passion for disease state awareness, industry, regulatory and competitive changes to deliver agreed results Basic Qualifications: Bachelor's Degree and 3 years of sales experience OR Associate degree and 6 years of sales experience OR High school diploma/GED and 8 years of sales experience Preferred Qualifications: Three or more years of sales experience within pharmaceutical, biotech or medical device industry Product or hospital sales experience in the areas of oncology, nephrology, dermatology, rheumatology, inflammation, cardiology, neurology, endocrinology, hepatology, gastroenterology or infectious diseases; and the diseases and treatments involved with these specialties Local market knowledge A Bachelor's degree in Life Sciences or Business Administration Adaptability with our Core Competencies: Planning and Organizing; Leveraging Business, Industry, and Technical Knowledge; Communicating with Impact; Driving for Results; and Cultivating Internal and External Relationships. Amgen is a Fortune 150 company operating in nearly 100 countries around the world. We invest in highly skilled, dedicated and collaborative individuals who are ready to contribute to our mission in meaningful ways and make a difference in the lives of our patients. 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.
Amgen Newbury Park, Thousand Oaks, CA, USA
Mar 31, 2020
Full time
Amgen utilizes suppliers and contract manufacturing partners to manufacture and supply injection molded device components to be used in our combination product offerings (drug delivery devices such as on-body and pen injectors). Ensuring reliable, high quality supply of these mechanisms requires appropriate consideration of the injection molding tools and processes proposed by our suppliers. The Engineering Projects ( Tooling/ Injection Molding) Senior Manager will be responsible for leading injection mold projects with external suppliers through RFP, mold design, construction, debugging, process development, and qualification to meet customer and production requirements including the planning, development, deployment, and implementation of new tools, changes to existing tools and the maintenance of existing tools. Additionally, the tooling engineer will collaborate with design engineers to evaluate part design and influence part design early in the development process to ensure manufacturability and reliability. Primary Responsibilities: Collaborate with design engineers and suppliers to evaluate & influence device parts and tooling designs to ensure design for manufacturability, reliability, efficiency, and process control requirements are accurately established and met Act as a tooling lead by participating in part design reviews as they relate to manufacturability, reliability and tool viability Evaluate, influence the design of injection molding tools including the runner, slides, ejection, vent and cooling system, draft angles, in collaboration with internal and external design teams to identify tooling design issues and de-risking opportunities prior to tool release at design review stage Develop new ideas to create innovation of performance of injection molding operations (cycle time, yield, uptime) and minimize risk Identify and implement novel tooling solutions (e.g. Coatings, Texturing, etc.) - specifically when/where to use them to improve reliability, and efficiency Review and approve tool CAD designs and changes and maintain accurate engineering documentation with regards to injection molding tooling including solid models, assemblies and prints Establish tooling/molding designs standards that align with device design stack-up tolerance requirements Lead integration of internal & external expectations/requirements in the areas of mold design, cavitation, prototyping and analysis with our device and mechanism suppliers Oversee sourcing and fabrication of tooling and assembly equipment including RFQ's with tool builders, visiting and auditing of tool builders and provide regular status updates to Supply and Development teams to ensure project timelines are met Support development of part handling and fixtures to reduce cosmetic defects during molding operations at suppliers Solve tooling and injection molding issues at suppliers and identify root cause and corrective actions Identify improvement and optimization opportunities to maximize robustness and efficiency of molding operations at suppliers Set & achieve ambitious cost saving goals utilizing Six Sigma methodologies and spearhead projects focused on systemic problems With our sourcing team, identify and develop high quality tooling and injection molding suppliers Ensure molding, handling and assembly processes are well defined, successfully communicated and accurately documented Basic Qualifications: Doctorate degree and 2 years of engineering experience, specifically in tooling or plastics manufacturing OR Master's degree and 6 years of engineering experience, specifically in tooling or plastics manufacturing OR Bachelor's degree and 8 years of engineering experience, specifically in tooling or plastics manufacturing OR Associate's degree and 10 years of engineering experience, specifically in tooling or plastics manufacturing OR High school diploma / GED and 12 years of engineering experience, specifically in tooling or plastics manufacturing AND Ability for international and domestic travel - up to 25% Preferred qualifications: Bachelor Degree in Engineering, Tooling and or Plastics degree preferred. Proficiency with 2D & 3D CAD software (SolidWorks preferred) 10+ years experience in high volume plastics environment, ideally experienced with both injection molding and extrusion Exposure to compliance standards with ISO 9000, TS16949, GMP and experience with Six Sigma and Lean Manufacturing methodologies Skilled with establishing processing parameters and documenting processes for injection molding manufacturing operations Strong problem solving and analytical skills Consistent track record participating with and creating a collaborative atmosphere to solve problems and improve product and process quality Demonstrated experience taking complex device design projects through end-to-end life cycle, including conceptualization, design, review, production planning, fabrication, & product validation Demonstrated experience influencing design for manufacturability of a part or system Strong grasp of engineering fundamentals Solid modeling experience Experience leading complex projects with challenging schedules Strong interpersonal & organizational skills Able to execute effectively with limited guidance Experience interfacing & maintaining relationships with suppliers 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. 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 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. 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.