Location: Hoofddorp (North Holland)
Duration: 6 months contract (extension is possible)
Working: Full time (40 hours)
Our client is one of the leading companies in biopharmaceutical industry, commited to promote new ways of treatment in serious diseases by developing innovative immunotherapies.
As QA Specialist you will be responsible to ensure that the Final Product meets the critical quality attributes. You will also be part of the disposition team by assisting with the preparation of binders. Other related tasks involve reviewing various GMP documentation.
Responsibilities-Performing a wide variety of QA activities by ensuring compliance to internal processes.
-Maintaining programs and processes by ensuring compliance with Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs).
-Conducting Corrective and preventive action (CAPA) and reviewing complex deviations.
-Contributing to projects related to QA.
Requirements-4+ years of experience in a GMP environment and a BSc degree OR
-2+ years of experience in a GMP environment related and MS (Master in Science).
Experience in Pharma/Bio industry is preferred
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