• Associate Director , Global Product…

    Otsuka America Pharmaceutical Inc. (Madison, WI)
    **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of clinical ... stored, and transported accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role has global responsibility for directing… more
    Otsuka America Pharmaceutical Inc. (12/19/25)
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  • Associate Director , Global Product…

    Otsuka America Pharmaceutical Inc. (Boise, ID)
    **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at ... way that is in accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role will direct Biologics Quality Assurance support,… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Associate Director , Engineering…

    Catalent Pharma Solutions (Manassas, VA)
    …Engineering, Process Engineering, Utility Systems, and Maintenance functions. The ** Associate Director , Engineering & Maintenance** will direct and lead a ... ** Associate Director , Engineering & Maintenance** **Position...**The Role** + Ensuring full compliance with OSHA and cGMP regulations at all times and working in concert… more
    Catalent Pharma Solutions (12/23/25)
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  • Associate Director , Equipment…

    Merck (Rahway, NJ)
    …Development and Facility Engineering (EDFE) Technology Engineer position will report to the Associate Director , Engineering and will be a member of the Modality ... systems. **Responsibilities of the EDFE Technology Engineer include the following:** The Associate Director , EDFE Technology Engineer role will serve as a… more
    Merck (01/09/26)
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  • Associate Director , Capital…

    Cambrex High Point (Charles City, IA)
    …world. Start a career where You Matter by applying today! Job Overview The Associate Director of Capital Projects is responsible for the strategic planning, ... equipment. The position ensures that all projects meet regulatory compliance requirements ( cGMP , FDA, OSHA), are delivered on time and within budget, and align… more
    Cambrex High Point (12/10/25)
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  • Associate Director - Business…

    Lilly (Lebanon, IN)
    …impact to our environment. **What You'll Be Doing** The Manufacturing & Quality (MQ) IT Associate Director -IT for LP2 will serve as the leader for the IT ... + Provide leadership in the development and execution of cGMP and/or improvement plans within the IT function and...to request an accommodation as part of the application process and any other correspondence will not receive a… more
    Lilly (11/08/25)
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  • Associate Director - Digital…

    Lilly (Indianapolis, IN)
    …who are determined to make life better for people around the world. ** Associate Director - Digital Engineering Solutions** **Organization Overview:** At Lilly, ... twins, computational modeling, edge/IoT, and analytics solutions. **Responsibilities:** The Associate Director - Digital Engineering Solutions position, within… more
    Lilly (11/15/25)
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  • Associate Director , Warehousing

    Merck (West Point, PA)
    **Job Description** ** Associate Director , Warehousing** Reporting to the Executive Director , North America Supply Chain Management, the Associate ... covers receiving, storage, distribution, planning and shipping of finished goods, in- process materials and sample products manufactured by our internal and external… more
    Merck (01/08/26)
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  • Associate Director , IT Regulatory,…

    Bristol Myers Squibb (Indianapolis, IN)
    …your application should be directed to Chat with Ripley. R1596697 : Associate Director , IT Regulatory, Clinical, and Enterprise Systems **Company:** ... aims to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory, Clinical and Enterprise Systems is an integral part of… more
    Bristol Myers Squibb (12/03/25)
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  • Associate Director , Pre-Commercial…

    Catalent Pharma Solutions (Greenville, NC)
    ** Associate Director , Pre-Commercial Quality Assurance** **Position Summary** + **100% on-site** Catalent is a global, high-growth, public company, and a leading ... handling capabilities, ideal for orphan or targeted drug development. This ** Associate Director , Pre-Commercial Quality Assurance** provides leadership and… more
    Catalent Pharma Solutions (01/07/26)
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