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    SR. Validation Specialist - Parsippany, United States - Insight Global

    Insight Global background
    Description
    Insight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full-time position. This position will be 5 days a week onsite, in Parsippany, NJ. This individual will play a crucial role in ensuring quality and compliance of pharmaceutical equipment. The ideal individual will have experience developing validation protocols for various process equipment and systems. This individual will have to execute validation test according to established protocols (IQ, OQ, PQ).

    We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day.

    We are an equal opportunity/affirmative action employer that believes everyone matters.

    Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances.

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    Knowledge of Capa and Deviations.
    5+ years Validation specialist or engineer within Pharma or Biopharma.

    Experience executing and writing test protocols Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ). Comprehensive knowledge of production processes.

    Experience with Trackwise or Veeva.

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