Job Description
:
As a QA Specialist you will support the QA management personnel in the execution and maintenance of the company's GxP Quality Systems.
Daily Responsibilities:
As the QA Specialist you will participate in the administration of the company's GxP Quality Systems (not limited to: Document Control System, Training Program, Deviations, and CAPA).
You will manage QA GxP documentation (audit files, raw data, reports, batch records, training records, deviations, CAPA, etc.)
Participates in internal audits and walkthroughs on behalf of the QA department to ensure site compliance to GMP.
Coordinating and providing site training on QMS elements such as GMP Induction, GMP refresher.
Education and Experience:
Knowledge of current Good Manufacturing Practices (cGMPs) (FDA / EMEA standards and quality systems).
Knowledge of OPEX Lean tools, and root cause analysis tools used for identifying and correcting deviations.
4+ years of relevant experience in a GMP environment related field and a BS.
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
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