- Bristol Myers Squibb (Summit, NJ)
- …for supporting the production of personalized cell therapy products for both global clinical trials and commercial supply. Potential areas of responsibility include ... These areas include creation/revision of documentation (ie SOP, change control, validation documentation, technical reports, etc.) required to support the production… more
- Bristol Myers Squibb (Princeton, NJ)
- …medicine, with a major focus on Companion Diagnostics (CDx) design control, validation , and clinical enablement, and the agility to pivot to GLP bioanalysis ... delivery of CLIA-based CDx initiatives: support design input/output, analytical validation , tech transfer, and clinical deployment across IHC and complementary… more
- Bristol Myers Squibb (Madison, NJ)
- …operating model . + Builds and continuously develops a high-performing global Quality team. + Fosters a culture of accountability, integrity, collaboration, and ... their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** This global executive role shapes and drives the Corporate Quality vision,… more
- Bristol Myers Squibb (Summit, NJ)
- …. **Position Summary** Subject matter expert supporting method transfer/ validation and routine testing of in-process, final product, and ... **Duties and Responsibilities** + Subject matter expert supporting method transfer/ validation and routine testing of in-process, final product, and stability… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …to ensure rebate eligibility and data consistency. + Perform Claim Level Detail validation . Review suspect claim records and determines if record should be disputed ... + Complete Medicaid analyzes and documentation on assigned states/programs. Communicate to manager for key findings and changes to state programs. + Provide backup… more
- Bristol Myers Squibb (Madison, NJ)
- …is seeking an Associate Director, Principal Product Quality Leader (PQL), in Global Product Quality to support commercial projects within the Cell Therapy ... for a commercial program along with associated regulatory expectations and global compliance requirements. T he individual will provide technical expertise and… more
- Bristol Myers Squibb (Princeton, NJ)
- …with deep expertise in assay and IVD development-including analytical validation , clinical development, manufacturing, and global regulatory submissions ... Summary** The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for biomarkers and diagnostics, focusing on early-stage… more
- TD Bank (Mount Laurel, NJ)
- …**Collaboration: Partner extensively with key stakeholders to ensure program success, including Model Development and Model Validation , ORM Internal Loss ... ability to manage regulatory relationships and defend methodologies to Model Validation and Audit.** **Strong leadership skills...We Are:** TD is one of the world's leading global financial institutions and is the fifth largest bank… more
- Bristol Myers Squibb (Princeton, NJ)
- …liaise with other BMS Enabling Functions including Information Technology, Finance and Global procurement and other key stakeholders to support the Law Department ... with internal groups and external vendors on delivery and validation of technology. + Develop reports in order to...for managing technology projects across the Department on a global basis. + Support the roll out education and… more
- Bristol Myers Squibb (Madison, NJ)
- …support across program(s) + Serves a key role in the implementation of the Global Clinical Development Strategy for the assigned book of work within an asset and/or ... + Clinical data review + Data interpretation; review and validation of CSRs + Regulatory requirements and documents (eg,...+ US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to… more