• Principal Scientist 1 - Chemical Research…

    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 (11/28/25)
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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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  • Director Quality Audits

    GRAIL (Durham, NC)
    …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... aspects of the Product Development Lifecycle supporting functions, including: Manufacturing Operations, Clinical Laboratory Operations, Program Management, Supply Chain,… more
    GRAIL (10/24/25)
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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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  • Aseptic Process Technician/Operator (GMP)

    Mentor Technical Group (Monroe, 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 (09/10/25)
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  • Process Technician I (Chemical Operator) - 2nd…

    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 ... generic markets for API and dosage form development and manufacturing . Your Work Matters. At Cambrex, we strive to...3 or more years' experience in a GMP Chemical Pharmaceutical pilot plant environment preferred. + 5 or more… more
    Cambrex High Point (09/18/25)
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  • Microbiologist I

    Catalent Pharma Solutions (Greenville, NC)
    …I primarily performs routine microbiological testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. ... dosage forms, including integrated formulation development, analytical services, commercial manufacturing , and packaging. This state-of-the-art facility has had over… more
    Catalent Pharma Solutions (12/03/25)
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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 (11/27/25)
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