• Lead Pharmacovigilance QC Specialist

    United Therapeutics (Trenton, NJ)
    …are as follows:** **Who we are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public ... a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.… more
    United Therapeutics (08/21/25)
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  • Director, Government Contracting and Analytics

    Sanofi Group (Morristown, NJ)
    …of government contracts including Medicaid State Supplemental Programs, State Pharmaceutical Assistance Programs (SPAPs), and the Federal Supply Schedule (FSS). ... development, and training of team members while fostering a culture of compliance , innovation, and continuous improvement. + Direct the efficient, timely and… more
    Sanofi Group (08/20/25)
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  • Application Support Manager - Sap

    Robert Half Technology (Bridgewater, NJ)
    …Participate in system upgrades, patching, and change management processes. + Ensure compliance with relevant regulatory and data governance standards, especially ... ability to manage cross-functional support initiatives. Prior experience in the pharmaceutical or biotechnology industry is highly desirable. Key Responsibilities: +… more
    Robert Half Technology (08/19/25)
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  • Manufacturing Operator 2nd shift (Compression)

    System One (Cranbury, NJ)
    …the production of solid oral dosage forms in a cGMP-regulated pharmaceutical environment. This role involves equipment setup, in-process testing, documentation, and ... and promptly report mechanical issues or abnormalities to the supervisor. Compliance & Documentation + Adhere strictly to safety protocols, cGMP guidelines,… more
    System One (08/03/25)
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  • Oncology, Divisional General Manager, Commercial…

    Sanofi Group (Newark, NJ)
    …account plans to drive Sarclisa utilization and net sales growth within regulatory and compliance guidelines. + Allocate resources across accounts, teams, ... all activities are conducted with integrity and in strict compliance with Sanofi policies and regulations. We are an...degree; MBA is highly valued. + 10+ years commercial pharmaceutical experience. + Proven experience in a sales leadership… more
    Sanofi Group (07/26/25)
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  • Sr. Director, Scientific & Medical Communications

    Taiho Oncology (Princeton, NJ)
    …Emotional Intelligence + Business Strategy & Organizational Insight + Risk Management & Regulatory Compliance + Budgeting & Financial Stewardship The pay range ... stakeholders to enhance scientific dialogue and engagement. The individual ensures compliance with regulatory policies, oversees vendor and budget management,… more
    Taiho Oncology (08/09/25)
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  • Senior Director, Managed Access Programs, Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …the primary point of contact for internal (Medical Affairs, Development, Commercial, Regulatory Affairs, Legal, and Compliance ) and external stakeholders to ... Experience: Minimum of 7+ years of experience in the pharmaceutical or biotechnology industry, with at least 3 years...of successfully managing MAPs across a disease area. + Regulatory / Compliance Knowledge: In-depth knowledge of… more
    Bristol Myers Squibb (08/13/25)
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  • Sr. Design Quality Engineer I

    Integra LifeSciences (Princeton, NJ)
    …processes are integrated into the overall product risk management process. ** Regulatory Compliance & Documentation:** + Ensure thorough documentation and ... quality systems, and a commitment to ensuring product safety and compliance . The ideal candidate should demonstrate proficient experience with quality management… more
    Integra LifeSciences (06/11/25)
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  • Clinical Research Director

    Sanofi Group (Morristown, NJ)
    …team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, marketing. + Advance ... full clinical study protocol. + Oversee the execution of clinical studies in compliance with internal SOPs, GCP, ICH guidelines and other regulations. + Review… more
    Sanofi Group (08/22/25)
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  • Senior Director Biostatistics

    Bristol Myers Squibb (Princeton, NJ)
    …institutes best practices with regards to planning, execution, interpretation and regulatory submission of clinical projects and studies. Provides guidance and ... defense as needed + Represents the company in interfaces with regulatory agencies globally + Drives strategy for processes improvement, contributes to… more
    Bristol Myers Squibb (07/15/25)
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