Banner Image

Location: Hoofddorp (North Holland)
Duration: 6 months contract (extension is possible) 
Working: Full time (40 hours)

Company

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.

Job description

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).

 

Other information
Experience in Pharma/Bio industry is preferred

 

Are you ready for your next challenge in your career? Then click the apply button below!

Need more iformation about either this or one of our other exciting positions? Don’t hesitate to contact us!