• Lead Validation Engineer or Specialist,…

    United Therapeutics (Silver Spring, MD)
    … professional looking to apply your expertise in a dynamic biotech and pharmaceutical environment? As a Lead Validation Engineer, Equipment, you'll be a ... title will be as a Validation Specialist) + 8+ years of relevant validation experience in a pharmaceutical /cGMP environment + Proficient knowledge of US and… more
    United Therapeutics (05/01/25)
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  • Validation Area Specialist

    Novo Nordisk (Durham, NC)
    …Support - OFP. Essential Functions + Participate & provide feedback to international corporate validation process group + Must be ability to work & communicate ... sites + Perform & review system, equipment, utility, & process revalidation per corporate science & risk-based validation...experience required + Minimum of five (5) years of validation related discipline experience in pharmaceutical or… more
    Novo Nordisk (04/23/25)
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  • Validation Engineer II

    Charles River Laboratories (Memphis, TN)
    validation protocols for cell processing equipment, lab instruments, cleaning, process , shipping, test method and other validation activities as ... that you can feel passionate about. **Job Summary** Reporting to the Manager Validation , the Validation Engineer II supports the qualification/ validation more
    Charles River Laboratories (05/27/25)
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  • Senior Principal Validation Engineer

    Curia (Albuquerque, NM)
    …Engineering, or relevant field + Fifteen (15) years relevant experience in pharmaceutical validation (aseptic/sterile product facility) + Experience with ... + Review and approve qualification, validation , re-qualification, and re- validation documents for equipment and manufacturing process protocols and… more
    Curia (04/04/25)
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  • Validation Engineer I

    Novo Nordisk (West Lebanon, NH)
    …The Position The person in this role will also be responsible for validation activities in several areas of pharmaceutical manufacturing including, but not ... or engineering + Work Experience + A minimum of three (3) years validation experience in the pharmaceutical or biotechnology industry + Experience preparing… more
    Novo Nordisk (05/17/25)
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  • Engineer - Validation I/II…

    Grifols Shared Services North America, Inc (Clayton, NC)
    …manages and completes all phases of assigned equipment, facilities, utilities and process qualification and validation activities. * Facilitates cross functional ... requires a minimum of 4 years' experience in the pharmaceutical industry **Engineer I** - Validation -...of the following: Utilities (HVAC, WFI, clean steam, compressed process air and nitrogen), Filtration (Sterile, depth, filter presses),… more
    Grifols Shared Services North America, Inc (05/13/25)
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  • Sr Process Controls & Validation

    Regeneron Pharmaceuticals (Rensselaer, NY)
    process development team. + Analyzing development studies, enrichment studies, process validation and characterization studies, chemical stability studies, ... Regeneron is looking for a Sr. Process Controls & Validation Scientist for...in-depth knowledge of liquid chromatography; experience in analytical chemistry, pharmaceutical sciences and protein characterization using a variety of… more
    Regeneron Pharmaceuticals (04/23/25)
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  • Principal Engineer, Validation

    Novo Nordisk (Bloomington, IN)
    …+ Understand other validation technical disciplines, such as cleaning, computer system validation , and process validation , and be able to integrate ... family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability...+ Execute validation protocols for cleaning method validation and cleaning process validation more
    Novo Nordisk (05/14/25)
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  • Senior Quality Validation Specialist

    Curia (Rensselaer, NY)
    …Review the Master Batch Records (MBRs) of commercial products and assess the need of process validation based on the proposed process changes + Conduct ... to support the overall project timeliness and on-going projects + Author/review/approve process and cleaning validation protocols and master plans, supervises … more
    Curia (04/10/25)
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  • Senior Director, QMS Process Owner…

    BeOne Medicines (San Mateo, CA)
    …operations. + Lead the design, implementation, maintenance, and continuous improvement of validation and manufacturing process elements in the QMS. + Define ... **General Description:** Senior Director, Business Process Owner (BPO) for GxP processes, with a...(BPO) for GxP processes, with a specific focus on ** Validation and select Manufacturing** processes within the **Quality Management… more
    BeOne Medicines (04/26/25)
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