• Clinical Research Quality Specialist B (Department…

    University of Pennsylvania (Philadelphia, PA)
    …and reports directly to the Associate Director, PSOM Office of Clinical Research Compliance . The Clinical Quality Specialist will work as part of the Compliance ... will work with senior team members to facilitate and conduct high quality compliance reviews, which include review preparation, conduct, close out and reporting, to… more
    University of Pennsylvania (08/03/25)
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  • Associate Director, Vendor Audits

    Bristol Myers Squibb (Devens, MA)
    …. **Position Summary** Reporting to the Senior Director, Competitive Compliance , the Associate Director, Vendor Audits, manages the relationship with ... with risk-based principles, collaborating on risk mitigation strategies to ensure compliance . **Key Responsibilities:** + Manage the relationship with and oversee… more
    Bristol Myers Squibb (09/12/25)
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  • US Regional Project Quality Lead

    Merck (De Soto, KS)
    …People Management, Pharmaceutical Industry, Problem Solving, Quality Compliance , Quality Operations, Regulatory Inspections, Site Qualification, USDA ... the QA/QC lead in establishing the quality assurance, quality control and compliance foundation in future project operations. Represents Quality within the project… more
    Merck (08/28/25)
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  • Staff Accountant

    Teledyne (Daytona Beach, FL)
    …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an ... Accountant at Teledyne Oil and Gas is responsible for compliance to GAAP, SOX404 and internal company policies and...to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high… more
    Teledyne (08/22/25)
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  • Associate Director, External Manufacturing…

    Merck (West Point, PA)
    …Knowledge of lean principles, equipment design, and preventative maintenance. . ** Regulatory ** - Global regulations and compliance requirements governing ... molded Device Components, Device Constituents, and Medical Devices used to deliver Pharmaceutical , Biologic, and Vaccine Products. Our team works with a "Safety… more
    Merck (08/18/25)
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  • Manager, Contracts & Transactions, Operational…

    Takeda Pharmaceuticals (Cambridge, MA)
    …Minimum of 5 years of experience in contract management, preferably within the pharmaceutical industry or a similar complex regulatory environment. + Knowledge ... in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more
    Takeda Pharmaceuticals (08/01/25)
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  • CSV Automation Engineer

    J&J Family of Companies (Wilson, NC)
    …Systems at all applicable points of the computerized system lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation (CSV) and ... a process for the validation of computer and automation systems ensuring compliance with required regulatory requirements. + Coordinates and executes training… more
    J&J Family of Companies (09/16/25)
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  • Validation Specialist

    Reckitt (Wilson, NC)
    …across computerized systems, manufacturing processes, and equipment. This role ensures compliance with regulatory requirements and internal quality standards, ... risk assessments, traceability, reports) in line with Reckitt and regulatory standards. + Ensure compliance with 21...+ 3+ years of experience in validation within the pharmaceutical or biotech industry. + Strong knowledge of cGMP,… more
    Reckitt (09/13/25)
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  • Associate Director, EH&S

    Curia (Springfield, MO)
    …risk assessment activities, and implement corrective action promptly to ensure company and regulatory compliance . Regulatory Knowledge, Compliance and ... organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At… more
    Curia (08/28/25)
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  • Software Quality Engineer II

    Abbott (Sylmar, CA)
    …non-product software. Ensures software systems are developed, validated and maintained in compliance with regulatory and business procedures. As a global leader ... Requirements and other relevant regulations for medical devices. Previous experience with regulatory body. Knowledge of software regulations and compliance (21… more
    Abbott (08/20/25)
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