• Project Engineer- ADD

    PCI Pharma Services (Rockford, IL)
    …Objective:** Design packages, processes, and tooling for assembly and packaging pharmaceutical products in a consistent, high-quality package that complies with ... planned expenditure. + Design assembly and package line layouts for pharmaceutical products weekly. Design/purchase tooling for Assembly and packaging equipment… more
    PCI Pharma Services (09/19/25)
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  • Principal Associate - QA Incoming Batch…

    Lilly (Durham, NC)
    …+ Performs batch disposition of raw materials, components, active pharmaceutical ingredient (API), and consumables to ensure high quality medicine ... and/or provide support during internal/external regulatory inspections. + Effectively review /approve GMP documents to ensure quality attributes are met (ie:… more
    Lilly (09/18/25)
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  • Labs FSP Scientist - GMP, Chemistry

    ThermoFisher Scientific (Boston, MA)
    …you, the employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. As a Scientist, ... values. Additional key responsibilities for the role on site at a major pharmaceutical company: + Oversee RSL method validations and/or method transfer activities to… more
    ThermoFisher Scientific (09/18/25)
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  • Associate Scientific Director Laboratory Sciences,…

    Charles River Laboratories (Reno, NV)
    …in compliance with SOPs, protocols, regulatory requirements as needed. + Review and approve Standard Operating Procedures (SOPs), protocols, policies, best practices ... 10 or more years' experience in the contract research or pharmaceutical industry conducting scientific research. Experience in a GLP (discovery) environment… more
    Charles River Laboratories (09/18/25)
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  • Pharmacist

    State of Arkansas (Little Rock, AR)
    …- $175,231 Job Summary The Pharmacist is responsible for providing pharmaceutical services within a state government facility. This includes dispensing medications, ... and Skills Extensive knowledge of pharmacology, therapeutics, pharmacokinetics, and pharmaceutical law. Strong understanding of drug interactions, side effects, and… more
    State of Arkansas (09/18/25)
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  • Manufacturing Specialist II

    Curia (Boston, MA)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... technology to deliver high quality sterile products to the pharmaceutical industry. This role also provides shift support to...entry and correct/troubleshoot entries into Ross ERP system + Review all Master Batch Records for content, clarity, and… more
    Curia (09/18/25)
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  • Principal Quality Officer

    Fujifilm (Research Triangle Park, NC)
    …and addressing sites exceeding agreed action limits) + Auditing: Peer- review colleagues' audit reporting + Auditing: Support companies/sites with consultative ... Science or similar + Profound experience (+10 years) withinGxPfrom the biotech/ pharmaceutical industry and extensive knowledge of relevant regulatory requirements +… more
    Fujifilm (09/18/25)
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  • HSE Permit Writer

    Lilly (Lebanon, IN)
    …constructing an advanced manufacturing facility for production of API (Active Pharmaceutical Ingredient) molecules located in Lebanon, IN. This facility is Lilly's ... supplies. + Perform safety audits and maintain an audit ready status. + Review and monitor relevant Standard Operating Procedures (SOPs) and SOP updates. Execute… more
    Lilly (09/18/25)
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  • Label Room Associate

    Unither Pharmaceuticals (Rochester, NY)
    Label Room Associate Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify ... Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 300 employees.… more
    Unither Pharmaceuticals (09/18/25)
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  • Principal Scientific Advisor

    Charles River Laboratories (Wilmington, MA)
    …may perform gap analyses, support due diligence procedures, and perform scientific review of discovery and/or safety assessment data or reports. This role provides ... immunology, etc.). * Experience: Minimum 20 years' experience in pharmaceutical /biotech sector, nonclinical contract research or consulting including at least… more
    Charles River Laboratories (09/18/25)
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