• Quality Systems Validation

    WuXi AppTec (St. Paul, MN)
    **Overview** The Quality Systems (QS) Validation Specialist serves as a key resource for providing oversight and guidance to ensuring equipment and ... and corrective actions. * Resource for equipment qualification and validation through quality systems (ie MasterControl, Non Conformances (NCE), Deviations,… more
    WuXi AppTec (01/22/25)
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  • Computer Systems Validation

    Robert Half Technology (New Haven, CT)
    Description We are offering an exciting opportunity for a Computer Systems Validation Specialist in New Haven County, Connecticut. As part of our team, you ... validation plans, protocols, and summary reports for computer systems to ensure regulatory compliance and quality ...Minimum of 3 years of experience as a Computer Systems Validation Specialist or similar… more
    Robert Half Technology (01/10/25)
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  • Systems Validation Specialist

    ICON Clinical Research (San Antonio, TX)
    Systems Validation Specialist - San Antonio,...**What ICON can offer you:** Our success depends on the quality of our people. That's why we've made it a ... our mission to shape the future of clinical development. We are currently seeking a Systems Validation Specialist to join our diverse and dynamic team. As a … more
    ICON Clinical Research (01/16/25)
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  • Validation Specialist

    Astellas Pharma (Westborough, MA)
    ** Validation Specialist , Quality Assurance** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, ... research programs. AIRM is headquartered in Massachusetts. Astellas is announcing a ** Validation Specialist , Quality Assurance** opportunity at their… more
    Astellas Pharma (01/16/25)
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  • Computer Systems GxP Validation

    University of Washington (Seattle, WA)
    …of Laboratory Medicine and Pathology** has an outstanding opportunity for a **Computer Systems GxP Validation Specialist ** **WORK SCHEDULE** + Temporary ... of computerized system validation principles, regulatory requirements, and quality management systems . + Excellent project management skills, with… more
    University of Washington (12/11/24)
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  • Quality Assurance Computerized System…

    Fujifilm (Thousand Oaks, CA)
    systems with all internal Quality requirements. **Job Description** **QA Computerized Systems Validation (CSV) Specialist ** The QA CSV Specialist ... + High school diploma with 9+ of applicable industry experience + Computerized systems validation experience in the pharmaceutical industry supporting cGMP … more
    Fujifilm (01/10/25)
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  • Sr. Quality Assurance Validation

    Bayer (Berkeley, CA)
    …and diverse minds to make a real difference, there's only one choice.** **Sr. Quality Assurance Validation Specialist - Berkeley, CA** **Sr. Quality ... Validation Specialist - Berkeley, CA** **PURPOSE** Quality Control Support SME to provide quality ...contractors as needed; + Utilize in-depth knowledge on GMP quality systems to support assessment of critical… more
    Bayer (12/22/24)
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  • Senior Cleaning Validation

    Catalent Pharma Solutions (St. Petersburg, FL)
    …vessels, clean-in place systems , and parts washers. The **Senior Cleaning Validation Specialist ** also responsible for supporting the design, execution and ... **Senior Cleaning Validation Specialist ** **Position Summary** Catalent, Inc....manufacture of drug product intended for human consumption. This validation group within the Quality Assurance department… more
    Catalent Pharma Solutions (11/22/24)
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  • Associate Validation Specialist

    Kedrion Biopharma (Melville, NY)
    …agencies, vendors, consultants, and other intended parties. The Associate Validation Specialist has the objective of maintaining high quality standards for ... hematology, immunology, neurology, and transfusion medicine. **JOB SUMMARY** The Associate Validation Specialist at Kedrion provides technical input to Kedrion's… more
    Kedrion Biopharma (01/22/25)
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  • Principal Specialist , Computer System…

    Boehringer Ingelheim (Athens, GA)
    …programs reflect Boehringer Ingelheim's high regard for our employees. The Principal Specialist , Validation manages all phases of higher level, more complex ... and requirements and are suitable for their intended purposes. The Principal Specialist , Validation will lead project management efforts for validation more
    Boehringer Ingelheim (01/11/25)
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  • QA Specialist III, QA Validation

    Fujifilm (College Station, TX)
    …understanding of Computer cGMP regulations and practices pertaining to computer validation principles, manufacturing processes, quality systems , engineering ... validation protocols and final reports and discrepancies for Quality Assurance. The QA Compliance Specialist III,...discrepancies for Quality Assurance. The QA Compliance Specialist III, QA Validation , will handle all… more
    Fujifilm (01/04/25)
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  • Validation Specialist

    Actalent (Azusa, CA)
    …Title: Validation SpecialistJob Description We are seeking a detail-oriented Validation Specialist to execute the day-to-day activities of our calibration ... and validation program, adhering to established procedures, deliverables, and monitoring...will also assist in sourcing and implementing electronic CAL/PM systems for equipment management and perform calibration and certification… more
    Actalent (01/18/25)
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  • Validation Specialist 2

    BioFire Diagnostics, LLC. (Lombard, IL)
    The Validation Specialist will develop, implement, and manage validation activities across multiple domains, including equipment, process, software, ... and internal procedures, minimizing risks while supporting operational excellence. The Validation Specialist will work closely with cross-functional teams,… more
    BioFire Diagnostics, LLC. (11/22/24)
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  • QA Specialist - Validation

    Regeneron Pharmaceuticals (Cambridge, MA)
    validation activities including analytical instruments, enterprise and laboratory computer systems validation , facility, utility, systems , and equipment ... We are seeking a ** Quality Assurance Specialist ** to join our...will support the lifecycle of GxP equipment, instruments, computer systems , facilities, and IT infrastructure critical to both internal… more
    Regeneron Pharmaceuticals (12/03/24)
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  • Validation Area Specialist - FFEx…

    Novo Nordisk (Clayton, NC)
    …compliance & technical reviews/approvals of protocols & protocol data + Author project quality masterplans (PQMP's), validation plans (VPL's), & other key ... source of expertise in the group for validating new systems + Ensure compliance of validation protocols...Master's Degree preferred + Minimum of seven (7) years validation or quality related discipline experience in… more
    Novo Nordisk (01/18/25)
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  • Cleaning Validation Specialist (CQV)…

    Verista (Los Angeles, CA)
    …experiences to enhance our collective expertise CQV Engineer Responsibilities: The Cleaning Validation Specialist for Operations is responsible for ensuring the ... + Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/ systems / software, and processes… more
    Verista (12/22/24)
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  • Validation Specialist

    Actalent (Azusa, CA)
    Description * Execute the calibration and validation program's day-to-day activities, adhering to established functional procedures, deliverables, and monitoring ... requirements. * Develop, review, and execute validation lifecycle documents for equipment and facilities commissioning, as outlined in the validation master plan… more
    Actalent (01/12/25)
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  • System Validation Specialist

    Charles River Laboratories (Newark, DE)
    …that you can feel passionate about. **Job Summary** Develop and manage validation and qualification activities associated with computerized systems to ensure ... ⦁ Write, revise, and oversee the approval of all required validation deliverables including: User Requirements Specification, Validation Plan, Functional… more
    Charles River Laboratories (01/16/25)
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  • CQV Specialist / Senior Validation

    Verista (Warren, NJ)
    validation in cGMP environments + Comprehensive knowledge of cGMP regulations, validation guidelines, and quality management systems + Exceptional ... + Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/ systems / software, and processes… more
    Verista (01/08/25)
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  • CQV Specialist / Senior Validation

    Verista (Warren, NJ)
    …with cGMP standards + Collaborate with cross-functional teams, including QC and Quality Assurance, to ensure successful execution and validation + Maintain ... + Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/ systems / software, and processes… more
    Verista (01/08/25)
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