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:
Assist with investigations and corrective and preventive action (CAPA) relating to quality systems.
Participates in authoring, reviewing, and approving Standard Operating Procedures (SOPs)/ Deviations/Change Controls and other types of controlled documents.
Participates in internal audits and walkthroughs on behalf of the QA department to ensure site compliance to GMP.
Organising site training on QMS elements such as GMP Induction, GMP refresher.
Education and Experience:
4+ years of relevant experience in a GMP environment related field and a BS.
Working 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.
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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