QA Associate

Hobson Prior working closely with a global pharmaceutical who is seeking a QA Associate to join their team in Switzerland. In this role, you will focus on batch record reviews, supportive project work, and ensuring compliance with cGMP standards. Your contributions will be crucial in supporting the timely release of GMP-relevant documents and batches. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Receive and document incoming materials such as executed batch records, work orders, and vendor labels. Prepare necessary documentation for batch record reviews, including analysis reports and specifications. Support the timely release of GMP batches, including labels, primary packed materials, and investigational medical

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