• Sr. Director, Process Engineering

    West Pharmaceutical Services (Kinston, NC)
    …engineering team, with the goal to improve and standardize the current manufacturing processes within the containment network, encompassing the elastomer and seal ... manufacturing processes. This individual will leverage experience and knowledge from the pharmaceutical or other highly regulated industries to develop the team's… more
    West Pharmaceutical Services (12/13/25)
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  • Inventory Analyst I/II

    Grifols Shared Services North America, Inc (Clayton, NC)
    …and place purchase requisitions to ensure no interruption to the manufacturing plan while ensuring attainment to inventory objectives. This position will ... in Production/Supply Planning/Inventory management preferably in a Biological or Pharmaceutical Environment. + Excellent oral and written communication skills. +… more
    Grifols Shared Services North America, Inc (12/11/25)
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  • Sr. Tech, Engineering

    Merck (Durham, NC)
    …Description** Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! The Sr. ... is a member of the Engineering team providing technical support to the manufacturing site. The site includes clean utilities, facilities equipment, manufacturing more
    Merck (12/10/25)
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  • Aseptic Process Technician/Operator (GMP)

    Mentor Technical Group (Durham, NC)
    …or related field preferred. + Experience: 1-3 years of aseptic/sterile manufacturing experience in a GMP-regulated facility ( pharmaceutical , biotech, or ... MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices… more
    Mentor Technical Group (12/10/25)
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  • Quality Assurance Specialist

    Catalent Pharma Solutions (Greenville, NC)
    …Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply ... time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing , Catalent supports the acceleration of development programs and… more
    Catalent Pharma Solutions (12/03/25)
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  • Associate Director, Clean Validation

    Fujifilm (Holly Springs, NC)
    …and executing Cleaning Validation (CV) activities for a large-scale biologics manufacturing facility in compliance with regulatory requirements, including 21 CFR ... 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging… more
    Fujifilm (11/20/25)
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  • Manager Quality Control

    Endo International (Raleigh, NC)
    …Manager is responsible for overseeing all QC activities to ensure pharmaceutical products meet regulatory requirements and internal quality standards. This role ... QC laboratories, supervising testing processes, and ensuring compliance with Good Manufacturing Practices (GMP) and applicable regulations (FDA, EMA, ICH). This… more
    Endo International (11/13/25)
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  • Talent Pipeline-Principal Scientist (Process…

    Cambrex High Point (Durham, NC)
    …to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing ... and more! Your Future Matters. Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety,… more
    Cambrex High Point (11/12/25)
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  • Talent Pipeline - Chemical R&D / Process Chemistry…

    Cambrex High Point (High Point, NC)
    …Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical ... partner in branded and generic markets for API and dosage form development and manufacturing . Your Work Matters. At Cambrex, we strive to build a culture where all… more
    Cambrex High Point (10/12/25)
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  • Regional Medical Scientific Director, Pulmonary…

    Merck (Raleigh, NC)
    …position **Experience | Skills** **Required** + Three years in the biotech/ pharmaceutical or healthcare environment + Three years clinical and/or research (beyond ... sponsored trials, or investigator-initiated trials) + Five years of prior pharmaceutical industry experience (Medical Scientific Liaison or other clinical, medical… more
    Merck (12/10/25)
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