44 jobs found in Emeryville

Mindtree is looking for Big data Architects, who has good experince in designingf architecture for large EDW or big data technology stack . You will be creating architectural principles/blueprint to support business goals, and develop IT frameworks that support EDW applications. Will be participating in design and architecture reviews and mentoring the data leads and developers with best practices. Desired Candidate Profile 10+ years Design/Architecture/implementation/consulting experience on Enterprise Data warehouse -On-premise/Cloud Platform Experience in Designing architecture for EDW/Data Lake on Public/Private Cloud and recommend the tools and techniques for implementation of cost effective and optimized solutions technologically. Create conceptual architectures and evangelize architectural vision, goals and design objectives to multiple audiences including client EA team. Experience in EDW data modelling using Star-schema/Snowflake and data architecting , Capacity Planning and Sizing Expertise on non-functional aspects (performance, HA, scalability, volume, security) Work on Architectural review discussions and prepare design solutions for stakeholder approvals, and subsequently used with scrum teams for implementation Should have hands-on experience in Database migration tools of cloud service providers Should have hands on experience in data orchestrations using cloud service provider tools Hands on experience in implementing EDW/Data lake application on Cloud platform Experience with SQL, Spark, Kafka, Go-lang, Scala, AWS, Python Create architectural principles/blueprint to support business goals, and develop IT frameworks that support EDW applications. Stream-processing systems such as Storm and Spark-Streaming Work with tech team to code and implement solutions in production and QA environments for permanent resolutions Soft skills Able to deal with diverse set of stakeholders and facilitate workshops Proficient in articulation, communication and presentation High integrity Problem solving skills & learning attitude Team player Educational Qualifications Technical degree required; computer science or electronics engineering degree desired; Industry Information Technology and Services Employment Type Full-time Mindtree Equal Employment Opportunity Policy Mindtree provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. Why Work with Us: Recognized for our employee learning and talent development practices Good work-life balance encouraged Recognition is the cornerstone of our culture Values-driven and engaged leadership About Mindtree Mindtree [NSE: MINDTREE] is a global technology consulting and services company, helping enterprises marry scale with agility to achieve competitive advantage. Born digital, in 1999 and now a Larsen & Toubro Group Company, Mindtree applies its deep domain knowledge to 350+ enterprise client engagements to break down silos, make sense of digital complexity and bring new initiatives to market faster. We enable IT to move at the speed of business, leveraging emerging technologies and the efficiencies of Continuous Delivery to spur business innovation. Operating in more than 15 countries across the world, we re consistently regarded as one of the best places to work, embodied every day by our winning culture made up of 21,000 entrepreneurial, collaborative and dedicated Mindtree Minds Welcome to possible ! Associated topics: data administrator, data architect, data engineer, data manager, data scientist, database, database administrator, mongo database administrator, sql, sybase

COMPANY DESCRIPTION At Santen, we're innovating therapies to improve the quality of life for patients worldwide. Our single focus in ophthalmology enables us to challenge unmet needs in the field-through passionate research, successful collaboration, and clarity of commitment. With over 130 years of investigative insight, Santen remains committed to the discovery, exploration, and development of ophthalmic therapies. As a global company, Santen is expanding to accommodate new and evolving initiatives in ophthalmic research, regulatory management, production, marketing, or distribution. Our clinical development network spans three continents, with centers in Europe, Japan, and the United States. We are in search of top talent to help us meet our aggressive and important goals. ABOUT THE POSITION: This position is responsible for implementing the North American-targeted Internal and External Communications focusing on increasing understanding and awareness of Santen, its values and mission, its people, products and pipeline consistent with Santen's global and regional communication strategies and policies. This position is expected to collaborate with Santen's Japan-based Corporate Communications Group in the development and implementation of the corporate communications strategy, plan development and execution, especially the messaging components for North America. ESSENTIAL DUTIES AND KEY DELIVERABLES: Participate in the development of a comprehensive Corporate Communications Strategy and link to overall global corporate objectives and priorities Lead the execution of the Corporate Communications Strategy for North America Develop and execute strategies to increase regional visibility and enhance internal awareness and external, targeting media and partners Partner with key internal stakeholders to support and develop internal and external communications efforts across various functions: Work with Commercial in supporting Marketing and Alliance Management, for product launch and partnership relationship by leading media management Work with HR to support employee communications and employer branding Support executive communications needs for internal and external audiences, including content / presentation development. Assist Medical Affairs in aligning activities with the corporate communication strategy regarding industry specific journals and media channels Support Headquarter Corporate Communications Group (CCG) on various investor relations needs such as presentations and leadership conference attendance Manage external vendors to ensure timely and quality delivery. Manage budget for all activities related to corporate communications. Manage and maintain communication standards against established corporate communication SOPs Manage crisis communications including planning, readiness, and response. Work with senior management and across the organization to align strategy/messaging Develop strategy and oversight of internal and external digital communications : support development and management of content for the Santen US website maintaining company web pages (Intranet and Inc Internet) Content creation and publishing of company newsletters (internal or external), news flash, digital online magazine, etc. Drive Santen US social media efforts, in collaboration with internal teams and external agencies, including identification of the most appropriate platforms to support business objectives and serve unmet patient needs Manage and develop activities of any direct reports within the function QUALIFICATIONS: Bachelor's degree required. Master's degree preferred. Minimum 7 years of corporate communications experience within multi-national companies and 3 years of corporate communication experience in a pharmaceutical or related life science industry. Demonstrated skills in translating business strategies to comprehensive internal and external communication strategies and influencing stakeholders Demonstrated ability to understand multiple, diverse stakeholders, anticipate impact of company actions on corporate reputation, and translate complex issues into clear, simple and consistent messages and themes. Brand management, media channel management and crisis communication management experience. Public relations and media training background a plus Strong writing, editing, and proofreading skills in the context of public relations Experience with social networks and implementation of social media marketing Experience with HTML, CSS, and working with content management systems (CMS) a plus For more information about our company and the work experience, please visit

ABOUT THE POSITION The Senior Manager, Publications and Scientific Congress (Pharmaceuticals), a part of the Global Medical Affairs (GMA), develops, deliver, and manages Global and US publications and scientific congress strategies and objectives across assigned therapeutic areas and molecules/products throughout the product lifecycle. This work encompasses Global and US publications and congress medical affairs booth planning, medical materials development, scientific education activities for external and internal audiences, and vendor management. The Senior Manager works closely with the therapeutic area medical leads and cross-functional partners across the organization in collaboration with the regions. This role ensures all timelines are met or exceeded and is responsible for process quality, efficiency, and consistency. The position reports to the Senior Director of Medical Communications, GMA. MAJOR DUTIES OF POSITION: Publications In collaboration with the therapeutic area medical leads, develops, maintains, and adjusts global publication strategies and imperatives detailing the appropriate scientific. communication across the assigned company portfolio and product lifecycle marketed and investigational products to relevant external audiences. Develops key scientific and communication objectives by having a strong scientific knowledge of the assigned therapeutic areas and molecules/products to drive credible, fair balanced, timely scientific publications. Coordinates and leads internal cross-functional publication team meetings and activities and external Medical Publications Steering Committees. Effectively and consistently communicates the publication strategy, tactics, and plan progress to internal business partners. Coordinates collaboration with authors, ensuring compliant author engagement; manages author meetings to facilitate content discussion and ensure appropriate content development process is followed. Reviews manuscripts, abstracts, and poster/slide content for accuracy and scientific rigor by having an in-depth knowledge of the scientific content; manages and facilitates the internal and external content review processes, including review and adjudication of comments. Masters and maintains up to date knowledge of ICJME and GPP 1 and 2, and Santen publications policy requirements; applies them in daily activities, including strategy development, tactical execution, and committee management. Acts as liaison between Medical Affairs Publications and external scientific content contributors. Develops and maintains tools and processes, including efficient and effective tracking systems (e.g., DataVision) for publication activities. Scientific Congress Develop, deliver, and manage the annual Scientific Congress strategy and tactics for assigned therapeutic area molecules/products across the organization in close collaboration with the regions. Partner with the therapeutic area medical leads and cross-functional partners to ensure the annual Scientific Congress strategy and tactics align with business needs and other components of the Medical Affairs Plans for the assigned molecules/products. Lead and manage core aspects of scientific congresses including medical/pipeline booth content/materials/design, training and booth coordination, scientific open house, and related activities. Facilitate scientific content development for the assigned therapeutic area medical teams and relevant stakeholders to be used in scientific congresses and other relevant activities. Provide oversight for review and approval of scientific and medical materials in compliance with corporate standards and government/industry regulations. Develop objectives/goals and performance metrics (e.g., medical information analytics, ethnographic research) for scientific congresses, including progress and trend reporting in collaboration with the therapeutic area medical leads and cross-functional partners. Lead the strategy and execution of scientific symposia, including collaboration with communications agencies, scientific faculty, driving symposium content development, and distribution of post-symposium reports. Develop and cultivate relationships with internal, cross-functional teams and external. partners involved in scientific congresses and other relevant scientific meetings across the organization (e.g., North America, EMEA, Asia, Japan). Other Accountabilities Coordinate and manage agencies and vendors across all aspects of publications, congress planning, and scientific content development. Acting as a guardian for high standards of compliance, ethics and safety; putting patients at the center of all actions. Managing assigned budgets to ensure consistent compliance with agreed parameters. KNOWLEDGE AND SKILL REQUIREMENTS: Advanced degree in Scientific Discipline or applicable Health Sciences field (e.g., PharmD, PhD, MD). Minimum of 6 years relevant pharmaceutical/biotechnology industry experience, with 3-5 years of publication planning experience within the pharmaceutical/biotechnology industry including submission processes for publications. Ophthalmology therapeutic area experience is preferred. Knowledge of pertinent external guidelines related to industry publications, and current standards of good publication practice. Experience with clinical trial reports and data presentation and interpretation preferred. Excellent communication, presentation, and negotiation skills. Strong interpersonal and partnering skills: has proven abilities to work effectively and efficiently in cross-functional, often virtual and matrix teams. Demonstrated experience of successfully influencing cross-functionally, cross-culturally, and cross-brands. Strong project and process management skills: proven abilities to effectively and efficiently manage multiple priorities, goals, objectives and tasks through to successful conclusion. Strong financial acumen: proven abilities for effective planning, development and oversight of project budgets and other resources. Awareness and understanding of regulatory guidelines (FDA, PDMA, PhRMA, etc.) and how they apply to scientific communications and medical education. Ability to travel up to 25% domestic and internationally to attend scientific congresses and relevant meetings.

ABOUT THE POSITION The Senior Manager, Publications and Scientific Congress (Pharmaceuticals), a part of the Global Medical Affairs (GMA), develops, deliver, and manages Global and US publications and scientific congress strategies and objectives across assigned therapeutic areas and molecules/products throughout the product lifecycle. This work encompasses Global and US publications and congress medical affairs booth planning, medical materials development, scientific education activities for external and internal audiences, and vendor management. The Senior Manager works closely with the therapeutic area medical leads and cross-functional partners across the organization in collaboration with the regions. This role ensures all timelines are met or exceeded and is responsible for process quality, efficiency, and consistency. The position reports to the Senior Director of Medical Communications, GMA. MAJOR DUTIES OF POSITION: Publications In collaboration with the therapeutic area medical leads, develops, maintains, and adjusts global publication strategies and imperatives detailing the appropriate scientific. communication across the assigned company portfolio and product lifecycle marketed and investigational products to relevant external audiences. Develops key scientific and communication objectives by having a strong scientific knowledge of the assigned therapeutic areas and molecules/products to drive credible, fair balanced, timely scientific publications. Coordinates and leads internal cross-functional publication team meetings and activities and external Medical Publications Steering Committees. Effectively and consistently communicates the publication strategy, tactics, and plan progress to internal business partners. Coordinates collaboration with authors, ensuring compliant author engagement; manages author meetings to facilitate content discussion and ensure appropriate content development process is followed. Reviews manuscripts, abstracts, and poster/slide content for accuracy and scientific rigor by having an in-depth knowledge of the scientific content; manages and facilitates the internal and external content review processes, including review and adjudication of comments. Masters and maintains up to date knowledge of ICJME and GPP 1 and 2, and Santen publications policy requirements; applies them in daily activities, including strategy development, tactical execution, and committee management. Acts as liaison between Medical Affairs Publications and external scientific content contributors. Develops and maintains tools and processes, including efficient and effective tracking systems (e.g., DataVision) for publication activities. Scientific Congress Develop, deliver, and manage the annual Scientific Congress strategy and tactics for assigned therapeutic area molecules/products across the organization in close collaboration with the regions. Partner with the therapeutic area medical leads and cross-functional partners to ensure the annual Scientific Congress strategy and tactics align with business needs and other components of the Medical Affairs Plans for the assigned molecules/products. Lead and manage core aspects of scientific congresses including medical/pipeline booth content/materials/design, training and booth coordination, scientific open house, and related activities. Facilitate scientific content development for the assigned therapeutic area medical teams and relevant stakeholders to be used in scientific congresses and other relevant activities. Provide oversight for review and approval of scientific and medical materials in compliance with corporate standards and government/industry regulations. Develop objectives/goals and performance metrics (e.g., medical information analytics, ethnographic research) for scientific congresses, including progress and trend reporting in collaboration with the therapeutic area medical leads and cross-functional partners. Lead the strategy and execution of scientific symposia, including collaboration with communications agencies, scientific faculty, driving symposium content development, and distribution of post-symposium reports. Develop and cultivate relationships with internal, cross-functional teams and external. partners involved in scientific congresses and other relevant scientific meetings across the organization (e.g., North America, EMEA, Asia, Japan). Other Accountabilities Coordinate and manage agencies and vendors across all aspects of publications, congress planning, and scientific content development. Acting as a guardian for high standards of compliance, ethics and safety; putting patients at the center of all actions. Managing assigned budgets to ensure consistent compliance with agreed parameters. KNOWLEDGE AND SKILL REQUIREMENTS: Advanced degree in Scientific Discipline or applicable Health Sciences field (e.g., PharmD, PhD, MD). Minimum of 6 years relevant pharmaceutical/biotechnology industry experience, with 3-5 years of publication planning experience within the pharmaceutical/biotechnology industry including submission processes for publications. Ophthalmology therapeutic area experience is preferred. Knowledge of pertinent external guidelines related to industry publications, and current standards of good publication practice. Experience with clinical trial reports and data presentation and interpretation preferred. Excellent communication, presentation, and negotiation skills. Strong interpersonal and partnering skills: has proven abilities to work effectively and efficiently in cross-functional, often virtual and matrix teams. Demonstrated experience of successfully influencing cross-functionally, cross-culturally, and cross-brands. Strong project and process management skills: proven abilities to effectively and efficiently manage multiple priorities, goals, objectives and tasks through to successful conclusion. Strong financial acumen: proven abilities for effective planning, development and oversight of project budgets and other resources. Awareness and understanding of regulatory guidelines (FDA, PDMA, PhRMA, etc.) and how they apply to scientific communications and medical education. Ability to travel up to 25% domestic and internationally to attend scientific congresses and relevant meetings.

R&D Research Associate We are currently developing immunoassays to test for COVID-19 and are looking for research associates to help accelerate this program and to also work on other assay development projects. This is an opportunity to work with a world class team to deliver an advanced, mobile medical diagnostic platform of urgent need to the healthcare industry. About You Creative self-starter Experience with laboratory practices Able to analyze and solve problems in an efficient and disciplined fashion Enjoy working in a collaborative, cross-disciplinary team environment Exceptional communication and organizational skills You are located in the San Francisco Bay Area Purpose of position: To assist in assay development and characterization. Perform quality control and experimental testing to support medical device products. Principal duties & responsibilities: Test chemical products and raw materials to ensure that materials meet specification and quality standards. Conduct tests, develop new and improved product tests and manufacturing process controls, including hands-on laboratory contributions. Provide sampling and analytical testing for materials and products before, during, and after the manufacturing process. Support non-conforming materials laboratory investigations, stability studies and validation activities. Create and revise specifications for material conformance. Participate in the characterization of the Nanomix platform and correlate results to materials and processing techniques. Maintain chemical and biological inventory to support manufacturing and research. Create documentation for test methods or systems, provide support to development and manufacturing groups. Maintain proper work environment and ensure all materials are properly handled, stored and discarded. Maintain lab notebooks and documentation Minimum Required Skills: B.S. or M.S. in Biochemistry, Bio- Engineering, Molecular Biology or related field. Should have 2+ years of experience in research and development of advanced technology or equivalent undergraduate level lab classes. Experience with a repertoire of techniques in molecular biology, biochemistry, and immunology. Experience with immunoassays and protein chemistry is a plus Experience in Industry, preferably having developed and transferred products to a manufacturing setting. About Nanomix: Nanomix is the leader in the development of mobile, affordable point-of-care diagnostics. We offer a handheld testing platform and assays that provide rapid, accurate, quantitative information for use in settings where time-to-diagnosis is critical to clinical decision making and improved patient care. Our goal is to expand access to quality health care by bringing diagnostics to the point of initial patient interaction, whether in the hospital or in pre-hospital, remote, or alternative settings. Nanomix is located in Emeryville, CA. For additional information, please visit the Nanomix web site at Associated topics: dietician, food scientist, histotechnologist, immunology, medical, microbiology, nephrology, nutritionist, physiologist, virus

Job ID: 175437 Emeryville office of our client seeks junior labor and employment associate attorney with 2-4 years of experience. The candidate will work primarily on cases within the area of Labor and Employment Law, including individuals and class actions. Must have extensive background drafting complaints, legal memorandum, discovery, and motions. Experience preparing for and taking depositions is essential. Experience building damage models is required. Experience overseeing the work of legal support staff is needed. Additional Skills: The candidate should have excellent research and writing skills. Must be detail-oriented. Should be highly motivated. Should be a quick learner and self-starter with a hard work ethic. BCG Attorney Search is the industry leader for placing candidates in permanent positions in law firms. Since 2000, our recruiters have placed several thousand attorneys and enjoyed extraordinarily high success rates with our candidates. As a BCG Attorney Search candidate, you have access to more opportunities than any legal placement firm in the United States. We are able to offer the most in-depth insight in the legal recruiting market thanks to our dedicated team of over 150 employees who mercilessly research, study and analyze the legal market. The depth and breadth of our research empowers us to place attorneys at rates that are unparalleled at any placement firm in the United States. Many of our recruiters make 30 to 40 placements per year, while recruiters at competitor firms are likely to make four or five. Unlike other placement firms that can only tell you about openings at major AmLaw firms, we place candidates of all backgrounds in firms of all sizes. While other legal recruiters only represent a narrow band of candidates from top law firms and top law schools, our research, firm contacts, and market insight allow us to place hundreds of candidates each year who do not fit this mold. It is rare that we do not get candidates we represent interviews and offers. No one in the world is better at legal recruiting and placement than BCG Attorney Search. BCG Attorney Search will confidentially review your application and will not forward your materials to the firm without first discussing the opportunity with you. If you have any questions about this opening, please contact us at .

Berkeley Lights is looking for a Field Applications Scientist to help us build the support structure for our West Coast clients. This role will serve as a key member of the Service and Support team, where you will help qualify, train and support customers in their own facilities on workflows developed for a rapidly evolving technology platform engaged in single cell assay, single cell culture, genomic evaluation, and therapeutics. You should be a scientist with great communication and customer service skills who is comfortable with advanced lab automation equipment, and willing to travel up to 70%. This is a highly visible position that prioritizes customer success and has direct ties to company leadership. Responsibilities: Support users by providing technical and scientific assistance for their workflows. Leverage strong structured problem-solving skills to identify and resolve customer needs. Provide voice of customer to internal development teams in product design, implementation and development areas, identify training and documentation gaps. Develop, coordinate and deliver product training to customers on software, application and/or equipment use, monitor customer installations within assigned territory/region to improve customer satisfaction and maintain customer relationships. Improve customer satisfaction and retention through continuing education on optimization and utilization by customer. Work with the internal BLI Team to develop troubleshooting, training and workflows demonstrating use, service, qualification, and installation of new products. Author, edit, and review technical documentation in conjunction with Technical writers, and contribute to the development and refinement of support processes and tools. Communicate with Account Managers and sales team to ensure all business needs are met. Required experience: M.S. or Ph.D. (preferred) in a scientific discipline or equivalent experience as a Field Application Scientist with exposure to biological applications. 5 + years' experience in scientific customer support and/or field applications support Willingness and ability to travel up to 50-70%, both domestically and internationally Familiarity with cell/tissue culture, cell-based assays, and microscopy platforms; experience in modern molecular and cell biology techniques desired. Three or more years of experience supporting customers in a commercial environment or experience training or leading in a laboratory or academic setting. Aptitude for understanding, communicating, and training scientific concepts, applications and methods. Highly motivated with strong problem-solving ability, strong organizational skills, and excellent verbal and written communications skill. Clear vision of and commitment to providing outstanding customer service. Self-motivated, willingness to take initiative to identify opportunities for improvement and take action. Berkeley Lights, Inc.'s (BLI) platforms allow thousands of parallel single-cell isolations using low intensity light in nanoliter volumes. Our platforms enable and streamline antibody discovery, production cell line development, single cell annotation and genomics, and point of care therapy workflows; our opto-nanofluidic technology delivers massive parallel processing. All operations are performed exclusively on our proprietary chip, leading toward unparalleled precision, accuracy, and computer control. We are motivated by three fundamental global challenges that face us today as we approach 8 billion people on earth: generating much broader access to food, energy and health care. Berkeley Lights has invented a platform technology that provides a rapid and predictable way to assess the function of living cells/organisms. With our technology, analysis and biology feedback are not only rapidly obtained at a fraction of the cost, but more importantly our customers find the specific biology that works the way they want it to work. This means predictable results in less time, for less money, and the ability to discover therapeutics or to find and engineer organisms that produce fuels, food, medicines, or clothing locally; anywhere in the world. Essentially, our technology enables the deployment of biology to the solve the largest problems that we face globally. This means everyone can have access to food, therapies, clothing, and energy which will drive strong global economic growth. We are looking for leadership team members with experience at scaling organizations to enable rapid and responsible growth over the very long-term. The power of engineering, brought to life. The California Consumer Privacy Act (CCPA) is effective January 1, 2020. Please read our California Consumer Privacy Act Disclosure Form regarding the CCPA and Berkeley Lights' required disclosures about the collection of personal information.

SENIOR CLINICAL DATA COMPANY DESCRIPTION At Santen, we're innovating therapies to improve the quality of life for patients worldwide. Our single focus in ophthalmology enables us to challenge unmet needs in the field-through passionate research, successful collaboration, and clarity of commitment. With over 130 years of investigative insight, Santen remains committed to the discovery, exploration, and development of ophthalmic therapies. As a global company, Santen is expanding to accommodate new and evolving initiatives in ophthalmic research, regulatory management, production, marketing, or distribution. Our clinical development network spans three continents, with centers in Europe, Japan, and the United States. We are in search of top talent to help us meet our aggressive and important goals. ABOUT THE POSITION: The Senior Clinical Data Scientist is responsible for Clinical Data Management (CDM) support for Santen's clinical studies following Santen's Standard Operating Procedures (SOP) and Guidelines. The person in this position should work as the lead clinical data manager for clinical trials and works closely with the lead clinician and biostatistician to develop the data management plan and electronic Case Report Forms (eCRF), build the Electronic Data Caption (EDC) system, author and program the Edit Check specifications, lead and guide the UAT of the EDC system, cooperate with lead EDC validation personal, lead data review, generate and solve data queries, create operational data sets, reconcile external data sets and safety data sets, perform database lock activities. ESSENTIAL DUTIES AND KEY DELIVERABLES: Participate in planning and support of clinical studies. Implement CDISC/CDASH standards in CDM. Prepare eCRFs and lead the team review of the forms ensuring compliance with Santen standards Build or participate in the EDC building. Develops programs and manages the edit check specifications and its implementation. Program EDC custom functions in SAS. Perform, oversee, and document EDC user acceptance testing. Perform and document EDC validation using GAMP5. Facilitate and document review of clinical data by other functional groups. Reconcile external data sets and safety database with clinical database using SAS Raise manual queries that result for data review and reconciliation activities. Resolve system and manual queries and perform database lock. Oversee CRO data managers and their data management activities for outsourced studies. Perform other duties as necessary as assigned by management. QUALIFICATIONS: Core compentencies, education, and experience. A minimum of eight (8) years in a pharmaceutical and/or a biotech company as a clinical data manager.. BS Degree or above Expertise in building electronic data capture systems such as Medidata RAVE, and in programming system edit checks. Expertise in electronic case report forms,, and data management plan development. Understanding of the MedDRA and WHODRUG coding processes. Strong project management, and written and verbal communication skills. Ability to mentor junior clinical data managers.. SAS Certification preferred. FDA/EMA inspection experience prefered For more information about our company and the work experience, please visit

SENIOR CLINICAL DATA COMPANY DESCRIPTION At Santen, we're innovating therapies to improve the quality of life for patients worldwide. Our single focus in ophthalmology enables us to challenge unmet needs in the field-through passionate research, successful collaboration, and clarity of commitment. With over 130 years of investigative insight, Santen remains committed to the discovery, exploration, and development of ophthalmic therapies. As a global company, Santen is expanding to accommodate new and evolving initiatives in ophthalmic research, regulatory management, production, marketing, or distribution. Our clinical development network spans three continents, with centers in Europe, Japan, and the United States. We are in search of top talent to help us meet our aggressive and important goals. ABOUT THE POSITION: The Senior Clinical Data Scientist is responsible for Clinical Data Management (CDM) support for Santen's clinical studies following Santen's Standard Operating Procedures (SOP) and Guidelines. The person in this position should work as the lead clinical data manager for clinical trials and works closely with the lead clinician and biostatistician to develop the data management plan and electronic Case Report Forms (eCRF), build the Electronic Data Caption (EDC) system, author and program the Edit Check specifications, lead and guide the UAT of the EDC system, cooperate with lead EDC validation personal, lead data review, generate and solve data queries, create operational data sets, reconcile external data sets and safety data sets, perform database lock activities. ESSENTIAL DUTIES AND KEY DELIVERABLES: Participate in planning and support of clinical studies. Implement CDISC/CDASH standards in CDM. Prepare eCRFs and lead the team review of the forms ensuring compliance with Santen standards Build or participate in the EDC building. Develops programs and manages the edit check specifications and its implementation. Program EDC custom functions in SAS. Perform, oversee, and document EDC user acceptance testing. Perform and document EDC validation using GAMP5. Facilitate and document review of clinical data by other functional groups. Reconcile external data sets and safety database with clinical database using SAS Raise manual queries that result for data review and reconciliation activities. Resolve system and manual queries and perform database lock. Oversee CRO data managers and their data management activities for outsourced studies. Perform other duties as necessary as assigned by management. QUALIFICATIONS: Core compentencies, education, and experience. A minimum of eight (8) years in a pharmaceutical and/or a biotech company as a clinical data manager.. BS Degree or above Expertise in building electronic data capture systems such as Medidata RAVE, and in programming system edit checks. Expertise in electronic case report forms,, and data management plan development. Understanding of the MedDRA and WHODRUG coding processes. Strong project management, and written and verbal communication skills. Ability to mentor junior clinical data managers.. SAS Certification preferred. FDA/EMA inspection experience prefered For more information about our company and the work experience, please visit

Biossance is seeking a Senior Packaging Development Manager, who will be responsible to oversee and develop primary and secondary packaging for specific product launches as determined by upper management. This position may be required to source and develop, work with the design concept, development, through production validation. Responsibilities Key contact on packaging in development and re-development. Manage the development of quality packaging in a cost-effective manner from concept to production while meeting product development calendar/deadlines. Develop and manage direct report(s). Coordinate draw downs, mock ups, proofs and initial pricing from suppliers. Manage and track day to day follow-up of samples, technical drawings and/or pricing via supplier status reports. Manage Package Development requests, orders and budget. Develop packaging timelines as required. Validate first production of primary and secondary packaging as required. Source packaging, attain samples and pricing and manage the approval process with all parties (internal brand as well as outside contractors/manufacturers). Familiarity with CAD and Solid Works drawings of primary and secondary components a plus. Develop specification sheets for all components for each project. Manage structural, functional and design proofs and mock ups to Creative Team, communicate with vendor on approvals or inform them of revisions given by the Creative Team. Responsible to keep status on all parts and serve as liaison between Marketing, Creative department, Operations and the manufacturer on all aspects of development and/or redevelopment. Controls design change process and serves as owner for all packaging design changes. May be called upon to develop, implement and maintain methods and/or processes in the fabrication of parts, components and final assemblies. Approve custom tooling and components for relevant components. Qualifications B.S. Degree in Packaging Engineering or related field of study. Min of 5 years of packaging development experience working on skincare, cosmetic or consumer packaged goods products Full working knowledge of materials, structural and functional design and tooling for primary and secondary packaging Knowledge of production, manufacturing, product integrity & production cycle timelines. Knowledge of component printing and graphic arts. Ability to perform high quality work in an efficient manner. PC workstation proficiency; Microsoft WORD, Excel, Outlook. Microsoft Projects a plus, but not required. Excellent written and verbal skills Embrace Amyris Core Values Adherence to Amyris Safety Policies and Procedures #LI-NE1 No Compromise Beauty™ Biossance is a clean beauty brand that uses biotechnology to create skincare products that are effective, sustainable and safe. We formulate with a No Compromise™ approach-proudly blacklisting over 2,000 potentially harmful ingredients. Only the most trustworthy and powerful make our final cut. Our Story It all began inside our Berkeley labs in 2003, where through biology and modern technology a plant-derived cure for malaria was created. Since then, over 120 million royalty-free treatments have been given, saving lives and communities. Inspired to keep positively changing the world through biotech, we turned to the ingredients people use on their bodies every day. And we asked how we could do better. Drawing on our rich history of science and sustainability, we create skincare products that are incredibly effective and safe without harming the environment. Because our standards for clean beauty are high-and our standards for ourselves are even higher. Biossance products are available at Biossance.com and Sephora. Amyris, a leader in industrial synthetic biology, uses its innovative bioscience solutions to achieve renewable products by converting plant sugars into hydrocarbon molecules. Amyris' molecules are used in wide range of specialty & performance chemicals, flavors & fragrances and in applications ranging from cosmetics to biofuels. Learn more at . Under the California Consumer Privacy Act of 2018 ("CCPA") , Amyris is required to inform California residents who are our job applicants ("Applicants") about the personal information we collect about you when you apply to a job on this site. As an Applicant, you have the right to know and understand the categories of personal information we collect about you, and the purposes for which the categories of personal information shall be used, pursuant to the CCPA. By clicking the "APPLY FOR THIS JOB" button below and submitting your job application, you agree you have reviewed the complete Privacy Notice for Employees, Independent Contractors and Job Applicants. If you have any questions regarding this information, please contact Amyris at As a VEVRAA Federal Contractor, Amyris is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Amyris complies with applicable state and local laws governing nondiscrimination in employment. If you are a recruiter or placement agency, please do not submit resumes to any person or email address at Amyris, Inc. prior to having a signed agreement. Amyris is not liable for and will not pay placement fees for candidates submitted by any agency other than its approved recruitment partners. Furthermore, any resumes sent to us without an agreement in place will be considered your company's gift to Amyris and may be forwarded to our recruiters for their attention.

The Social Media and Community Manager will implement the company's social media strategy, developing brand awareness, generating inbound traffic and encouraging product adoption. This role coordinates with the internal Marketing and PR teams to support their respective missions, ensuring consistency in voice and cultivating a social media referral network. Role Expectations: Manage Social Media marketing campaigns and day-to-day activities including: Curate relevant content to reach the company's ideal customers Create, curate, and manage all published content (images, video and written) Monitor, listen and respond to users in a "Social" way while cultivating leads and sales Conduct online advocacy and open stream for cross-promotions Develop and expand community and/or blogger outreach efforts Oversee design (ie: IG stories, Facebook Timeline cover, profile pic, thumbnails, ads, landing pages, Twitter profile, and blog) Compile report for management showing results (ROI) Become an advocate for the Company in Social Media spaces, engaging in dialogues and answering questions where appropriate Develop a strategy and implement a proactive process for capturing customer online reviews Monitor online ratings and respond accordingly Monitor trends in Social Media tools, applications, channels, design and strategy Identify threats and opportunities in user generated content surrounding the business Report notable threats to appropriate management Analyze campaigns and translate anecdotal or qualitative data into recommendations and plans for revising the Social Media campaigns Monitor effective benchmarks (best practices) for measuring the impact of Social Media campaigns Analyze, review, and report on effectiveness of campaigns in an effort to maximize results Displays in-depth knowledge and understanding of Social Media platforms, their respective participants (Facebook, Twitter, Yelp, Google+Local, YouTube, Instagram, Pinterest etc.), and how each platform can be deployed in different scenarios Maintains excellent writing and language skills Enjoys a working knowledge of the blogging ecosystem relevant to the Company's field Displays ability to effectively communicate information and ideas in written and video format Exceeds at building and maintaining sales relationships, online and off Is a Team player with the confidence to take the lead and guide other employees when necessary. (ie: content development, creation and editing of content, and online reputation management) Experience: agency or in house has successfully managed, curated and written for notable profiles (please link to previous work) Manage social media campaigns and day-today activities Online advocacy, writing editorial, community-outreach efforts, promotions, etc. Manage presence in social networking sites including Instagram, Facebook, Twitter and other similar community sites, posting on relevant blogs, and seeding content into social applications as need Advocate of the Company in social media spaces, engaging in dialogues and answering questions where appropriate Implement the social media strategy, coordinating with stakeholders across the Company to ensure its Effectiveness and encouraging adoption of relevant social media techniques into the corporate culture and into al of the company's products and services Act as editor of Purecane Newsletter/ Blog and manage all postings and scheduling Manage a Blogger outreach program and build an active brand ambassador network to spread the word about the Company and its' products Monitor effective benchmarks for measuring the impact of social media programs, and analyze, review and report on effectiveness of campaigns in an effort to maximize results Provide feedback/insights gained from social media monitoring into the Marketing team, to help them evolve their strategies in a timely fashion Monitor trends in social media tools, trends and application. Desired Skills and Experience: Bachelor's Degree in Journalism, English, Communications or related field At least 5-7 years in social media, public relations, journalism, corporate communications or related Strong project management or organizational skills In-depth knowledge and understanding of social media platforms and their respective participants (Facebook, Digg, YouTube, Twitter, Flicker, etc.) and how they can be deployed in different scenarios Knowledge of blogging ecosystem relevant to the Company's field Ability to effectively communicate information and ideas in written and verbal format, and build and maintain relationships Team player with the confidence to take the lead and guide other departments when necessary. Good technical understanding and can pick up new tools quickly Have a good knowledge of principles of Search Engine Optimization (SEO) Public relations, Marketing, Sales, Community Management experience, a plus Excellent writing skills and attention to detail Creative brainstorming ability. #LI-DJ1 Amyris, a leader in industrial synthetic biology, uses its innovative bioscience solutions to achieve renewable products by converting plant sugars into hydrocarbon molecules. Amyris' molecules are used in wide range of specialty & performance chemicals, flavors & fragrances and in applications ranging from cosmetics to biofuels. Learn more at . Under the California Consumer Privacy Act of 2018 ("CCPA") , Amyris is required to inform California residents who are our job applicants ("Applicants") about the personal information we collect about you when you apply to a job on this site. As an Applicant, you have the right to know and understand the categories of personal information we collect about you, and the purposes for which the categories of personal information shall be used, pursuant to the CCPA. By clicking the "APPLY FOR THIS JOB" button below and submitting your job application, you agree you have reviewed the complete Privacy Notice for Employees, Independent Contractors and Job Applicants. If you have any questions regarding this information, please contact Amyris at As a VEVRAA Federal Contractor, Amyris is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Amyris complies with applicable state and local laws governing nondiscrimination in employment. If you are a recruiter or placement agency, please do not submit resumes to any person or email address at Amyris, Inc. prior to having a signed agreement. Amyris is not liable for and will not pay placement fees for candidates submitted by any agency other than its approved recruitment partners. Furthermore, any resumes sent to us without an agreement in place will be considered your company's gift to Amyris and may be forwarded to our recruiters for their attention.

Research Associate, Biochemical Assay Development Position Summary Metagenomi is a start-up biotechnology company headquartered in Emeryville, CA. We are developing next-generation human therapeutics using novel CRISPR gene-editing systems discovered in naturally occurring microbes. We are seeking a motivated individual for a research associate position that will specialize in molecular biology, biochemical assay development, and biochemical screening. This person will be expected to tackle a variety of challenges as an integral part of Metagenomi's Characterization Team by helping us discover novel gene editing machinery. Candidates should be enthusiastic, passionate, and have a desire to change the world. Responsibilities ● Perform biochemical assays using purified protein, crude extracts, or bacterial handling using sterile technique ● Carry out preparatory work for assays including cloning, PCR, and nucleic acid purification ● Develop, optimize, and automate discovery screens ● Gather and analyze experimental data under the direction of the research scientist or group leader, present to key stakeholders ● Prepare accurate and timely data summaries and contribute to writing of reports ● Other duties as assigned Minimum Qualifications ● BS or MS in biology or related discipline and 2+ years of relevant research experience ● Biochemical and molecular biology techniques such as gel electrophoresis, cloning, DNA and RNA purification ● Experience working with wet and dry lab scientists ● Excellent organizational skills and both oral and written communication skills ● Track record of challenging oneself to enhance scientific skills and knowledge ● Ability to think strategically, manage time and workflow, and work independently as well as in a results-oriented research team Preferred Qualifications ● 2+ years of experience working in a molecular biology laboratory ● Gene editing by CRISPR Cas9 ● Handling purified protein and using sterile technique (including plating recombinant bacteria on selection media) ● Experience with liquid handling robotics or performing 96-well plate format assays ● Experience with qPCR or NGS ● RNA purification and handling ● Experience with enzyme characterization such as kinetics or affinity measurements Why work at Metagenomi? ● We are passionate about developing next-generation gene editing cell therapies and we are focused on unlocking the potential of microbial products for use in healthcare, biotechnology, and industry ● Metagenomi is a dynamic group and we value quality, creative and agile thinking, and excitement about our mission ● We offer competitive salaries, benefits (Healthcare, matching 401(k) retirement safe harbor plan) ● We offer equity in our early stage startup Metagenomi.co is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.

Slingshot Biosciences has developed a breakthrough synthetic cell platform that is enabling global access to advanced, accurate diagnostics. Our current focus is centered around flow cytometry and hematology, and we are poised to expand into engineered cell therapy with an upcoming product launch. We are looking for a talented team member with general molecular bioloy, biochemistry, and general chemistry experience. Ideally, qualified candidates will have been exposed to protein conjugation chemistry and immunochemistry. Qualified applicants must have 2+ years of biochemistry and protein chemistry experience either an advanced degree program, or industrial setting, with a demonstrated history of success. Please be prepared to provide 3 references. Candidates will be interviewed via teleconference prior to an on-site meeting with the team. Candidate must be local or must be willing to relocate for the position. We offer the following: Flexible work schedule and vacation time Health, vision, life, and dental benefits 401k matching Freedom to attend conferences and publish non-confidential work Close affiliation with leading academic and goverment research institutes

Slingshot Biosciences has developed a breakthrough synthetic cell platform that is enabling global access to advanced, accurate diagnostics. Our current focus is centered around flow cytometry and hematology, and we are poised to expand into clinical markets with an upcoming product launch. We are looking for a team member with strong biochemistry experience, specifically around protein conjugation chemistry. Sector experience in hematology and/or flow cytometry is highly recommended although not necessary. Qualified applicants must have 5+ years of biochemistry and protein chemistry experience in an industrial setting, with a demonstrated history of success. Please be prepared to provide 3 references and to prepare a case-study during an on-site interview. Candidate must be local or must be willing to relocate for the position. We offer the following: Flexible work schedule and vacation time Health, vision, life, and dental benefits 401k matching Freedom to attend conferences and publish non-confidential work Close affiliation with leading academic and goverment research institutes

This position will be located at our Emeryville, CA or Syracuse, NY office. Innovative Interfaces (a ProQuest Company) is dedicated to providing leading technology solutions (software) and services that empower Libraries and enrich their users worldwide. Visit us at We employ many diverse and energetic professionals across the globe-from California to Dublin, Ireland to New Delhi, and points in between. Innovative's software products are used every day by people in over 50 countries in over 20 languages at academic, public, government, law, and special Libraries. JOB DETAILS The Director of Business Systems reports to the Vice President of I.T. and will work closely with the respective stakeholders, building empathy and understanding of the business' processes and challenges, ensuring the Business Systems Team is setup to provide a high quality output to satisfy the needs of the business. This role includes creating and managing project plans, participating in the definition of business requirements and design, as well as contributing to building, testing, deploying, supporting and enhancing business applications. This individual will apply high-level communication and problem-solving skills to guide and assist users and team members on issues related to the design, development, and deployment of mission-critical information systems. DUTIES AND RESPONSIBILITIES Essential Functions: • Oversee Business Processes including Quote to Cash, Procure to Pay, Project Management, Lead Generation, Case and Issue Management. Review proposed changes and enhancements to these processes, develop plans to implement them. • Demonstrate ability to balance technical skills with soft skills; ability to transform end-user needs/functional requirements into technical requirements and build scalable solutions. • Partner with the leadership team to create and maintain a robust Business Application Environment, reporting services and application architecture roadmaps. Ensure these roadmaps are well understood throughout the business functions and meet emerging requirements • Develop Policies and Procedures, and Documentation that the Business Systems department adheres to. • Recognize and identify potential areas where existing policies and procedures require change, or where new ones need to be. • Familiarity with Testing and Quality Control standards as well as industry standard change management processes. • Develop, test, document and maintain out of the box and/or custom solutions, integrations and data migration elements of a NetSuite Implementation. • Manage relationships with vendors, technology partners and contract providers to ensure they are meeting requirements set forth in signed agreements. • Ensure Business Applications comply with 3rd Party Financial and IT Audits, also Security & Privacy regulations. • Create and manage the Business Systems budget and provides input in the administration of related budgets. EXPERIENCE AND QUALIFICATIONS Required Education, Licenses, and Certifications: • Bachelor's degree in related field. • Certified NetSuite Administrator. Experience: • Minimum 4 years of relevant experience implementing and maintaining Enterprise level applications associated with financial/operational systems. • Minimum 5 years of people management experience, preferably in Business Systems function. • Extensive working knowledge of NetSuite ERP, Marketo, Salesforce. • Experience managing third-party ERP consultants. • Exceptional analytical and problem-solving skills, and experience applying these skills to resolve operational accounting process and system issues. • Experience in mapping and analyzing business processes, understanding use cases for key systems and developing business requirements. • Experience with managing a departmental budget, procurement to payment life cycle, comparing budget vs. actuals. Critical Knowledge, Skills, and Abilities Requirements: • Excellent oral and written communication skills. • High level of knowledge in accounting and finance. • Strong project management skills with the ability to successfully manage multiple competing priorities and projects. • Ability to be a team player and be highly organized. • Ability to multitask and drive numerous projects simultaneously. • Ability to communicate effectively with internal stakeholders across all levels within the organization. • Ability to plan and prioritize workload. • Demonstrate high commitment to quality customer service. Preferred • Master's degree highly preferred. ADDITIONAL REQUIREMENTS OR INFORMATION • Although duties are typically performed during normal business hours, occasional off-hours work may be required to meet customer and/or business needs. *Nothing in this job description restricts management's rights to assign or re-assign duties and responsibilities to this job at any time. Innovative Interfaces (a ProQuest company) is an Equal Opportunity and Affirmative Action employer. It provides equal employment opportunities to all employees and applicants for employment without regard to race, color, sex, national origin, age, religion, disability, or any other legally protected status and takes affirmative action to recruit, employ, train, and promote qualified minorities, women, covered veterans, and individuals with disabilities.

Job Title AAS (Azure Analysis Services) Developer Type of Role Direct Hire Job Location Emeryville, CA Industry Information Technology Salary Range NA CVPartners is working with a client in the East Bay that is looking for an AAS Developer to join their team on a full-time basis. The ideal candidate will have intermediate to advanced skills with AAS development (Tabular Models specifically), data warehousing, modeling (logical and physical), analysis etc. to assist in an Azure implementation. BullHorn Job ID 444797