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Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.Employer: Bristol-Myers Squibb CompanyPosition: Scientist I (ref. #1341) Location: 1 Squibb Drive, New Brunswick, NJ 08903Duties: Responsible for binding and cell-based potency assay development, optimization, validation, and testing in a Good Manufacturing Practice (GMP) environment to support the company’s portfolio of preclinical, clinical-stage and commercial biologics by using experience with flow cytometry, use of associated software (e.g. FlowJo, BD FACSDIVA), and lentiviral transduction; GraphPad Prism Software. Perform immunoassays, binding assays and cell-based potency assays to support: release and stability, drug biological activity characterization for health authority filings, extended characterization from process and product changes, Critical Quality Attributes (CQA) assessments, and in-process testing to support process development. Develop, optimize and validate bioassay and immunoassay biological characterization and potency methods for biologic, cell therapy or gene therapy products in Immuno-oncology and other disease areas. Provide progress updates at appropriate intervals and milestones. Collaborate with discovery, early development, process sciences groups, analytical, and quality groups. Understands rationale behind molecule engineering and recognize and appropriately address molecular liabilities. Partner with discovery and process development teams to determine impact of product variants. Author and/or review Standard Operating Procedures (SOPs), protocols, reports, training documents, and documents related to sample testing, instrument maintenance, calibration and qualification. Participate in preparation of health authority submissions. Secure appropriate resources to generate complete biological characterization package. Author relevant potency and biological characterization sections. Organize, interpret and present scientific data to management.Requirements: Masters degree (or foreign equivalent) in Biotechnology, Molecular Biology, Immunology plus 18 months of post-Master’s experience in pharmaceutical industry showing demonstrable ability in the skill set described above.This position is eligible for our employee referral program.Contact: Katherine Russaw Horton3551 Lawrenceville Road
Princeton, NJ 08540
Resume.com@bms.comBristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
