• 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 ... Specifications. If completed by an external company, the computer systems validation (CSV) specialist will be responsible for obtaining these documents… more
    Unither Pharmaceuticals (05/08/25)
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  • Validation Specialist

    Kedrion Biopharma (Melville, NY)
    _Kedrion is looking for a_ **_Validation Specialist - Computer Systems_** _to join our team and play a critical role in ensuring the compliance and reliability ... EU, and GAMP 5 standards._ **_Job Role and Responsibilities_** + _Lead validation projects for GxP systems -authoring and executing protocols and documentation… more
    Kedrion Biopharma (05/06/25)
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  • Sr. Specialist /Principal Specialist

    Boehringer Ingelheim (St. Joseph, MO)
    …similar manufacturing environment. + Relevant experience must include conducting computerized systems validation in a regulated industry such as pharmaceutical ... similar manufacturing environment. + Relevant experience must include conducting computerized systems validation in a regulated industry such as pharmaceutical… more
    Boehringer Ingelheim (07/26/25)
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  • Senior QA Validation Specialist

    Curia (Rensselaer, NY)
    Senior QA Validation Specialist - CSV Systems...experience working in a cGMP regulated industry specific to computer systems validation + ... Engineer Summary: The Senior QA Validation Specialist - CSV Systems Engineer is an...team. This role is responsible for supporting Quality Management Systems and Computer System Validation more
    Curia (06/20/25)
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  • Senior Validation Specialist

    Regeneron Pharmaceuticals (Cambridge, MA)
    We are seeking a highly skilled, self-motivated **Senior Validation Specialist - CSV** to ensure compliance of computerized systems with regulatory ... 11, GAMP 5, and Annex 11. **As a Senior Validation Specialist , a typical day might include:**... validation documentation and explanations and communicates company's computer validation policies. + Generating, reviewing, editing,… more
    Regeneron Pharmaceuticals (07/26/25)
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  • Lead/Sr Computer System Validation

    Cognizant (Muskegon, MI)
    …engineering project work. The CSV Lead will have 10 plus years of experience of automation systems computer systems validation in a GMP environment. The ... Sr/Lead CSV Specialist Cognizant Technology Solutions in LSMG is seeking...MES, ABB as well as other DCS and OT systems . **Requirements** : The Validation Lead responsibilities… more
    Cognizant (07/09/25)
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  • Senior Validation Specialist

    Catalent Pharma Solutions (St. Petersburg, FL)
    **Senior Validation Specialist ** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... offer a broad range of integrated formulation. The **Senior Validation Specialist ** with guidance from the ...procedures and processes to assure that Catalent facilities, equipment, computer , and supporting systems are fit for… more
    Catalent Pharma Solutions (07/24/25)
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  • Lead Specialist , QA Validation

    Catalent Pharma Solutions (Harmans, MD)
    …This position will provide continuous improvement support to process, equipment, utilities and computer systems and serve as the key Quality resource for the ... **Lead Specialist , QA Validation & Engineering** Catalent...as IQ/OQ/PQ for various equipment such as bioreactors, chromatography systems , controlled temperature units, filling/stoppering machines, autoclaves and critical… more
    Catalent Pharma Solutions (07/24/25)
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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....department is responsible for ensuring that all facilities, processes, equipment/ systems and automated equipment used for GMP/GLP critical purposes… more
    Catalent Pharma Solutions (06/18/25)
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  • Validation Quality Specialist

    Belcan (Durham, NC)
    …* Assists in the development of cGMP operating procedures that relate to process, computer systems , and equipment validation . * Assures compliance with SOPs ... Validation Quality Specialist Job Number: 358838...* Ensures current Good Manufacturing Practices (cGMP) and Quality Systems are adhered to throughout the evaluation, review and… more
    Belcan (07/22/25)
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