• Validation Lead ( GxP…

    Cognizant (Boston, MA)
    **Cognizant Technology Solutions** is looking for " ** Validation Lead ( GxP & Life Sciences Domain)** " to join in our team of IT professionals in a ... and Digital Business Assurance in Gartner Magic Quadrant! ** Validation Lead ( GxP & Life Sciences Domain)** **Location: Boston, MA (Remote)** **Required… more
    Cognizant (09/09/25)
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  • GxP Validation Lead : QA…

    Cognizant (Boston, MA)
    ** GxP Validation Lead : QA Life Sciences (Remote)** **_This is a remote position open to any qualified applicant in the United States_** Cognizant ... Technology Solutions is seeking a " ** GxP Validation Lead : QA** ** Life Sciences(Remote)",** to join our team of IT professionals in a permanent role. If… more
    Cognizant (09/10/25)
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  • Senior Manager, IT - GxP Computer Systems…

    Bristol Myers Squibb (Indianapolis, IN)
    …global leader in radiopharmaceuticals. The Sr. Manager, IT - GxP Computer Systems Validation & IT Process Lead is an integral part of bringing RayzeBio's ... **Working with Us** Challenging. Meaningful. Life -changing. Those aren't words that are usually associated...Responsibilities** + Manage and Deliver applicable risk-based Computer Systems Validation across RayzeBio Digital and IT teams. + Ensure… more
    Bristol Myers Squibb (09/09/25)
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  • IT Compliance Expert - GxP

    Nestle (Bohemia, NY)
    …to business stakeholders. Your will be responsible for the selection, development, validation and maintenance of enterprise GxP systems, including but not ... and manage them through the IT governance process, drive the planning, implementation, validation and support of enterprise GxP applications. If you are… more
    Nestle (08/19/25)
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  • Validation Lead (ALM) : QA…

    Cognizant (Boston, MA)
    ** Validation Lead (ALM) : QA Life...Validation and test scripts that confirm systems meet GxP and CSV/CSA standards, ensuring they are audit-ready. . ... Sciences(Hybrid)** Cognizant Technology Solutions is seeking a " ** Validation Lead (ALM) : QA** ** Life ...management tool Regulatory Knowledge: Strong understanding of FDA, EMA, GxP , and 21 CFR Part 11 requirements; experience with… more
    Cognizant (09/10/25)
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  • Head Global Quality Equipment and Facilities…

    Takeda Pharmaceuticals (Lexington, MA)
    …**Job Description** **OBJECTIVES/PURPOSE** * Provides governance and oversight to all GxP Engineering and associated Equipment validation activities including ... oversight for GxP systems such as evaluation and approval of all GxP classification evaluation and system validation activities. * Collaborates with Global… more
    Takeda Pharmaceuticals (08/28/25)
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  • Veeva QMS Validation and QA Lead

    CGI Technologies and Solutions, Inc. (Burlington, MA)
    …QMS processes. * Ensure compliance with GxP and 21 CFR Part 11 regulations, and lead validation efforts using tools such as HP ALM to maintain validation ... **Veeva QMS Validation and QA Lead ** **Category:** Business...be successful in this role:** * Bachelor's degree in Life Sciences, Computer Science, Engineering, or related field. *… more
    CGI Technologies and Solutions, Inc. (08/20/25)
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  • Principal Specialist, Validation

    Boehringer Ingelheim (Athens, GA)
    …validation project activities at the BIAH location from concept through process validation ensuring GxP regulatory compliance continues as outlines in BIAH's ... and requirements and are suitable for their intended purposes. The Principal Specialist, Validation will lead project management efforts for validation … more
    Boehringer Ingelheim (08/16/25)
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  • Validation Engineer

    Actalent (Winston Salem, NC)
    Validation Engineer Job Description This validation Engineer is tasked with supporting laboratory instrumentation and computerized systems within a GMP-regulated ... principles, GMP regulations, and internal policies. + Manage qualification, validation , and periodic review activities for laboratory instruments and computerized… more
    Actalent (09/05/25)
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  • QA Lead Technical Operations - CAPA

    Sokol Materials & Services (Skillman, NJ)
    QA Lead Technical Operations - CAPA Job Location Devens,...Level of relevant experience in a GMP, GCP, or GXP with at least 8 years focused on product ... * Review and approve documents related to Quality, Quality Control, Validation , and Automation. * Review and approve Standard Operating Procedures (SOPs).… more
    Sokol Materials & Services (07/31/25)
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