Are you passionate about quality and precision? Join this team as a QA Associate and help ensure top-tier standards every day.
Proclinical is seeking a QA Associate QMS to support the timely release of GMP-relevant documents and batches, ensuring compliance with cGMP standards. This role involves routine tasks such as batch record reviews and supportive project work within the TRD GCS environment.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
Key Skills and Requirements:
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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