- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …skilled and experienced professional to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream processes. This ... performance issues at CDMOs. + Analyze upstream process data (via CPV program , campaign summaries) to monitor performance, identify trends, and propose process… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director , Government Contracting and Analytics **Location:** Morristown, NJ or Cambridge, MA **About the Job** This position is ... lead with Contract Development and Pricing team for assessing government program implications of commercial contracting activities and ensure the appropriate… more
- Bristol Myers Squibb (Princeton, NJ)
- …NJDEP. + Serve as the Cyclotron Particle Accelerator Safety Officer (PASO). Regulatory qualifications/requirements to be eligible as a PASO are noted in ... use, training, and disposition of all X-ray generating devices. Included regulatory requirements and responsibilities such as registrations, surveys, operations, and… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …fate/effects studies and environmental risk assessments according to appropriate international regulatory guidelines. This role will lead and participate on diverse ... the opportunity to participate in other aspects of the Product Stewardship program (eg, global research projects, environmental support of sites, extended producer… more
- Bristol Myers Squibb (Princeton, NJ)
- …on translational data generated to support asset development and contribute to regulatory submissions. This individual will work on cross-functional project teams to ... scientists, as well as BMS members from clinical, medical, commercial, regulatory , and diagnostics. Individual will also engage with external academic… more
- Bristol Myers Squibb (Princeton, NJ)
- …activities for the pipeline and supports late stage portfolio for regulatory , translational development and life cycle management. Translational Development drives ... are not limited to, the following:** + Designs and implements program -specific late development biomarker/translational plans, responsible for aiding in creation of… more
- BeOne Medicines (Pennington, NJ)
- …duties or QA projects assigned according to business needs. Depending on the program supported, this position may include some travel. **_Essential Functions of the ... and vendor qualification. + Development of all necessary SOPs, ensuring regulatory compliance in conjunction with being appropriate both clinical and commercial… more
- Bristol Myers Squibb (Summit, NJ)
- …strategies, process risk assessments, etc), inspection readiness, and technical regulatory submissions. The Sr. Principal Engineer will support commercial product ... Lead production related investigations, ensuring compliance with internal standards and regulatory requirements. + Own Stage III validation (CPV) reports including… more
- Merck (Rahway, NJ)
- …or significant issues affecting quality and efficiency. + Interprets complex regulatory requirements for various audiences, reviews draft policies and standards. ... Management, Business, Chemical Biology, Compliance Investigations, Deviation Management, Global Program Development, Good Manufacturing Practices (GMP), Management Process, Organic… more
- Bristol Myers Squibb (Princeton, NJ)
- …Diseases. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K).… more
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