• Director , QA Data Integrity

    ThermoFisher Scientific (Greenville, NC)
    …degree with relevant work experience. + 10 years plus experience in pharmaceutical manufacturing , or pharmaceutical laboratory testing with confirmed ... Schedule** Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office **Job Description** The QA… more
    ThermoFisher Scientific (10/02/25)
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  • Associate Director -Quality Control

    Lilly (Concord, NC)
    …of the Quality Control Laboratories at Lilly's Concord, North Carolina pharmaceutical manufacturing site. Responsibilities include technical and administrative ... and processes necessary to provide GMP lab testing in support of manufacturing operations. **Responsibilities:** The Associate Director , Quality Control, will… more
    Lilly (11/13/25)
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  • Associate Director Technology

    Amgen (Holly Springs, NC)
    …providing process automation and information systems solutions and support to manufacturing organizations in the biotechnology or pharmaceutical industries. + ... us and transform the lives of patients while transforming your career. **Associate Director Information Systems** **What you will do** Let's do this. Let's change… more
    Amgen (10/12/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... analysis techniques, fostering their professional growth and expertise in pharmaceutical stability studies. + Collaborate cross-functionally with analytical team… more
    Otsuka America Pharmaceutical Inc. (11/25/25)
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  • Associate Director . Technical Project…

    Merck (Raleigh, NC)
    **Job Description** Digital Chemistry, Manufacturing , and Controls (dCMC) is a cross-divisional initiative that will enable the pipeline by establishing a digital ... continuum of data from development through manufacturing for our products and processes. dCMC intends to...a minimum of 8 years of experience in the pharmaceutical industry + MS in chemistry, engineering, or related… more
    Merck (11/27/25)
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  • Director , Supply Chain

    Catalent Pharma Solutions (Greenville, NC)
    …solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing , and packaging. The Director , Supply Chain role ... ** Director , Supply Chain** **Position Summary:** + 100% on-site...Work with specialist and technical functions (eg Engineering, Quality, Manufacturing , etc.) to ensure problem-free introduction of new products.… more
    Catalent Pharma Solutions (11/26/25)
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  • Associate Director , Field Access Manager…

    Merck (Raleigh, NC)
    **Job Description** Associate Director , Field Access Management The Associate Director , Field Access Management serves as the leader to a team of subject-matter ... access strategy. **Minimum Requirements:** * Bachelor's Degree; 9+ years in the pharmaceutical /biotech industry * Minimum 3 years of experience in patient support,… more
    Merck (11/27/25)
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  • Team Lead East - Senior Director , US…

    Merck (Raleigh, NC)
    **Job Description** **Role Summary** + The Regional Medical Scientific Senior Director Team Lead (RMSD TL) is a credentialed therapeutic and disease expert (MD, PhD, ... workforce. **_Strategic Planning and Execution_** + In alignment with the Executive Director of US Medical Affairs, engages with cross-functional partners to develop… more
    Merck (11/20/25)
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  • Senior Director , Global Process Owner…

    Lilly (Durham, NC)
    …to make life better for people around the world. **Responsibilities** The Senior Director , Global Process Owner for Quality Risk Management, as a leader within the ... System. The Global Process Owner will consult with Lilly manufacturing facilities, external supplier organization, marketing affiliate quality operations,… more
    Lilly (11/20/25)
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  • Director , Parenteral Sterility Assurance

    Lilly (Raleigh, NC)
    …role provides ad-hoc technical support to Lilly PR&D, external contract manufacturing , and non-sterile drug substance (API) manufacturing . **Responsibilities:** ... the agenda within PR&D to ensure the needs of Manufacturing are met, and the control strategies are fit...scientists in the fields of sterility assurance and applied pharmaceutical microbiology + Understanding of cGMP's, policies, procedures, and… more
    Lilly (11/14/25)
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