• Legend Biotech USA, Inc. (Raritan, NJ)
    …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a QA Validation Specialist III as part of the Quality team based in Raritan, ... NJ.Role OverviewThe QA Validation Specialist role is an exempt level...position with responsibilities for providing quality oversight over the validation and qualification activities for equipment, systems, computer more
    HireLifeScience (11/11/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …strongly preferred.Experience with Manufacturing Execution Systems (MES) design/development and validation is preferred.Experience with Computer System ... of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Specialist , QA Process Excellence as part of the Quality team based in Raritan,… more
    HireLifeScience (12/09/25)
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  • Cipla (Fall River, MA)
    Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM ... is searching for experienced candidates for the position of Documentation Specialist . The Documentation Specialist is responsible for the creation… more
    HireLifeScience (10/30/25)
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  • Cipla (Fall River, MA)
    Job Title IT Specialist Organization Name InvaGen Pharmaceuticals, Inc Location 927 Currant Rd., Employment Type (Hourly/ Full Time) Exempt/Professional Salary Range ... role will perform IT Systems Support including Systems Implementation, Validation , Administration etc., for Manufacturing, Packaging, Warehouse, Quality etc., IT… more
    HireLifeScience (12/05/25)
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  • Insmed Incorporated (NJ)
    …GxP system owners. Who You Are:3+ years' hands on experience in a validation role with responsibility for computer systems specifically LIMS, Empower, BMRAM, ... management, and reviews of validated systems. Author CSV Documents ( Validation Plans and Summary Reports) Assist/co-author requirements, testing, specification, and… more
    HireLifeScience (11/01/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma.Legend Biotech is seeking Document Control Specialist as part of the Quality team based in Raritan, NJ.Role OverviewThe ... QA Document Control Specialist role is an exempt level position with responsibilities...and approve SOPs, and other documentation.Drive continuous improvement.Have advanced computer skills to increase department's productivity, as well as… more
    HireLifeScience (12/03/25)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionThe Specialist , Advanced Analytics will work with our partners across GCTO to help address critical business questions beyond simple descriptive or ... prescriptive, & machine learning/AI capabilities Build prototypes for early user validation Identifying and acquiring data based on business needs to enhance… more
    HireLifeScience (12/12/25)
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  • Takeda Pharmaceutical (Los Angeles, CA)
    …About the role: Takeda's Los Angeles Quality Control team is seeking a QC Specialist III who will serve as the primary LIMS subject matter expert (SME) for ... full lifecycle implementation of LabWare changes-requirements, design, configuration, testing, validation , and deployment. Evaluate and implement LIMS functionalities and… more
    job goal (12/15/25)
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  • The Computer Merchant, LTD. (Manassas, VA)
    JOB TITLE: Test & Evaluation Engineering Support Specialist JOB LOCATION: Manassas, VA WAGE RANGE*: 39-40.66 JOB NUMBER: 25-03809 JOB DESCRIPTION: Our client, a ... defense contractor, has an immediate opening for a Test & Evaluation Engineering Support Specialist to work from their Manassas, VA facility. Our client are on the… more
    job goal (12/14/25)
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  • Computer Systems Validation

    Unither Pharmaceuticals (Rochester, NY)
    Computer Systems Validation Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that ... and Design Specifications. If completed by an external company, the computer systems validation (CSV) specialist will be responsible for obtaining these… more
    Unither Pharmaceuticals (11/25/25)
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  • Senior Validation Specialist I,…

    Catalent Pharma Solutions (Kansas City, MO)
    **Senior Validation Specialist I, BioAnalytics Computer System Validation (CSV) & Compliance** **Position Summary:** Catalent, Inc. is a leading global ... in Kansas City, MO (KCM) is hiring a Senior Validation Specialist I, BioAnalytics CSV & Compliance.... is primarily responsible for leading, implementing and managing Computer System Validation (CSV) and Data Integrity… more
    Catalent Pharma Solutions (11/13/25)
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  • Principal QA Validation Specialist

    Regeneron Pharmaceuticals (Troy, NY)
    We are hiring a Principal QA Validation Specialist to support validation and qualification of computer systems within IOPS. The Principal QA ... Validation Specialist would also plan, coordinate and participate in compliant computer system validation (CSV) process for systems which require formal … more
    Regeneron Pharmaceuticals (12/06/25)
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  • Lead Validation Specialist

    System One (Princeton, NJ)
    Lead Validation Specialist Location: Remote (Preference for East Coast candidates) Salary: $125,000-$150,000/year + bonus potential About the Role We're seeking ... an experienced Lead Validation Specialist with a strong background in clinical systems and computer systems validation to join our growing team. In this… more
    System One (12/14/25)
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  • Sr. Specialist , Manufacturing Quality…

    AbbVie (North Chicago, IL)
    …YouTube and LinkedIn. Job Description Purpose: The primary responsibility for the Quality Validation Specialist is the Quality oversight and overall approval of ... in Manufacturing and/or Packaging, Quality or Engineering including 4 major validation subjects (eg Computer , Equipment, Cleaning, Process, etc.) preferred… more
    AbbVie (11/11/25)
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  • Jt614 - Validation Specialist

    Quality Consulting Group (Villalba, PR)
    …systems on existing work instructions and processes. + Prepare and execute computer system validation protocols and generate comprehensive reports. + Develop ... + Technical writing knowledge + Organization and Communication skills + Process Validation and Computer software validation knowledge + Experience in SDLC +… more
    Quality Consulting Group (12/13/25)
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  • Compliance Validation Specialist

    TestPros (Sterling, VA)
    …Analysis, Cyber Security, NIST SP 800-171 Assessment and Compliance, Computer Forensics, Software Assurance, Software Testing, Test Automation, Section 508 ... and WCAG Accessibility Assessment, Localization Testing, Independent Verification and Validation (IV&V), Quality Assurance (QA), Compliance, and Research and… more
    TestPros (11/18/25)
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  • Validation Scientist

    Kelly Services (Bristol, TN)
    **Senior Validation Specialist - Direct Hire (Permanent)** **Location:** Bristol, TN **Reports to:** Technical Operations / Quality Leadership **Schedule:** ... **LabVantage LIMS** , scheduled for go-live in late February/early March. + Oversee ** computer system validation ** (CSV) for LIMS, Waters Empower (HPLC), SAP… more
    Kelly Services (11/26/25)
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  • Specialist , Product Sterilization…

    Terumo Neuro (Aliso Viejo, CA)
    **12989BR** **Title:** Specialist , Product Sterilization (Temporary, 6-8 month contract) **Job Description:** Salary Range $36.50 - $40.00/hour Financial ... quality assurance projects and activities to meet the sterilization validation requirements of medical products. Lead sterilization process commissioning, initial… more
    Terumo Neuro (12/10/25)
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  • Senior Specialist , Digital & Data Quality

    Merck (Wilmington, DE)
    …and/or maintenance of training programs in the principles of computerized systems validation , computer software assurance, and regulatory requirements in ... Accountability, Adaptability, Business Continuity, cGMP Regulations, Change Management, Communication, Computer System Validation (CSV), Deviation Management, Disaster… more
    Merck (12/09/25)
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  • NPI Quality Specialist

    DEKA Research & Development (Manchester, NH)
    The New Product Introduction (NPI) Quality Specialist supports design transfer activities and quality operations in an innovative, fast-paced, medical ... development, review and maintenance of control plans, risk management files, validation protocols, process capability studies; and other QMS documentation to support… more
    DEKA Research & Development (11/15/25)
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