• Senior Supplier Quality Engineer I - External…

    Integra LifeSciences (Princeton, NJ)
    …candidate will work closely with commercial manufacturing team members, and ExM/ Contract manufacturing leadership and maintains knowledge of current GMP expectations ... including product disposition, manufacturing instructions, change controls, and process validation documentation. + Monitor quality performance of the ExM sites… more
    Integra LifeSciences (07/03/25)
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  • Project Manager

    Catalent Pharma Solutions (Greenville, NC)
    …is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients ... is responsible for leading and directing multiple client projects within the contract manufacturing division. The Project Manager will work closely with key project… more
    Catalent Pharma Solutions (07/12/25)
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  • Quality Investigations Specialist II

    Curia (Rensselaer, NY)
    …where our work has the power to save lives. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering ... with pharmaceutical and biotech companies to provide life-saving treatments to...Systems as they related to SOP creation and control, Validation of Computerized Systems per Code of Federal Regulations,… more
    Curia (07/10/25)
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  • Senior Scientist, Analytical Development

    Catalent Pharma Solutions (San Diego, CA)
    …Analytical Development** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... annually. Catalent Pharma Solutions in San Diego is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical more
    Catalent Pharma Solutions (06/18/25)
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  • Scientist - Analytical

    Actalent (Sanford, NC)
    …PM (occasional weekend work as needed) Start Date: Targeting September 1, 2025 Contract Duration: 2 years (potential for extension) Pay Range: $35-$55/hour (based on ... experience and qualifications) Placement Type: Contract Minimum Education: Bachelor's degree Disqualifiers: No GMP experience...Analytical to join the Quality Control Method Transfer and Validation (MTV) team in Sanford, NC. This role supports… more
    Actalent (07/22/25)
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  • Research Scientist - Regulatory Submission / CMC

    ThermoFisher Scientific (Boston, MA)
    …in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, ... employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. **Key… more
    ThermoFisher Scientific (06/28/25)
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  • Quality Assurance Associate - Drug Product…

    Lilly (Indianapolis, IN)
    …through effective quality oversight of North, Central and South American contract manufacturers and alliance partners. This oversight covers the process steps ... of selection, pre- validation / validation , ongoing operations and termination. DPEM Quality...communication and maintaining effective relationships with our alliance partners, contract manufacturers, and internal business customers. The QA Lead… more
    Lilly (05/31/25)
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  • Associate Director Quality Control

    Regeneron Pharmaceuticals (Rensselaer, NY)
    …the qualification and testing strategy, the oversight of the QC method validation of the methods for incoming components including visual inspection, functional ... and method transfer to or from other internal sites, partners companies, and contract manufacturing companies. Experience in gene therapy and cell therapy is a plus.… more
    Regeneron Pharmaceuticals (05/09/25)
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  • Sr. Scientist Peptides API EM

    Lilly (Indianapolis, IN)
    …Lilly, a leading innovation-driven corporation is developing a growing portfolio of pharmaceutical products by applying the latest research from its own worldwide ... the world! **Organization Overview:** Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a… more
    Lilly (07/24/25)
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  • Process Development Senior Scientist - Synthetics…

    Amgen (Cambridge, MA)
    …responsible for late phase analytical development, including method development, method validation , method transfer, process and product development support, and GMP ... chiral purity and structure elucidation using mass spectrometry + Manage activities at contract manufacturing and testing sites. + May lead method transfer to CMO or… more
    Amgen (07/20/25)
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