• Vice President, Corporate Quality

    Bristol Myers Squibb (Princeton, NJ)
    …quality and compliance across Bristol Myers Squibb. As a trusted advisor to senior leadership, the VP ensures alignment with business goals and global regulations, ... Owner Network that will develop and sustain the QMS working collaboratively with senior leaders across R&D, GPDS and Commercial. + Oversees SOP governance, document… more
    Bristol Myers Squibb (12/18/25)
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  • Finance Modeling Specialist

    Novo Nordisk (Plainsboro, NJ)
    …interact with stakeholders across the Finance organization with frequent interaction at the manager , senior manager and director level. Moreover, the job ... will not manage any contingent workers. Essential Functions + Model development and implementation + Data, logic, and quality... development and implementation + Data, logic, and quality validation + User support and continuous improvement + Cross… more
    Novo Nordisk (12/05/25)
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  • Healthcare Clinical Documentation Specialist

    Deloitte (Morristown, NJ)
    Healthcare Clinical Documentation Specialist - Senior Consultant Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and ... Recruiting for this role ends on Feb 28, 2026 Work you'll do As a Senior Consultant in our Regulatory, Risk, & Forensic Healthcare Practice, you will have the… more
    Deloitte (11/21/25)
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  • Director, GTS TechOps ERP

    BeOne Medicines (Pennington, NJ)
    …peers to define, sponsor, and execute continuous improvements. + Proven leadership at a senior level directing a team of manager direct reports and associate ... meet business needs. Implementation of SAP: + Understand business model and processes and work with key stakeholders on...ERP long term roadmap. + Work with SAP Project Manager , (external) Consulting Team and (internal) Core Business Team… more
    BeOne Medicines (12/30/25)
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  • Associate Director, Principal Product Quality Lead

    Bristol Myers Squibb (Madison, NJ)
    …role is preferred + Expertise is Lentiviral Vector manufacturing or analytics with validation experience is a plus. + Expertise in GMP compliance, global regulations ... rational manner, and demonstrated ability to work as a senior management team member and to engage and influence...+ US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to… more
    Bristol Myers Squibb (12/24/25)
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  • Director, Early Precision Medicine Regulatory…

    Bristol Myers Squibb (Princeton, NJ)
    …with deep expertise in assay and IVD development-including analytical validation , clinical development, manufacturing, and global regulatory submissions through ... scientific and regulatory concepts into clear, actionable insights for senior leadership and cross-functional teams. Builds strong partnerships across internal… more
    Bristol Myers Squibb (12/03/25)
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  • R&D Engineer III - Customization/Customer Support…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …as an extension of "Tier 2" Pharm Systems capabilities per Customer Engagement Model (CEM). He/she proposes potential inventions and inform BD in accordance with ... quality assurance principles. He/she reports to Customization/Customer Support R&D Product Care Manager . **Job Description** We are **the makers of possible** BD is… more
    BD (Becton, Dickinson and Company) (12/11/25)
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