QA Specialist

QA Specialist - Denmark, Copenhagen - 2-4 Month Contract

Our client, a global organisation within the pharmaceutical industry, needs a QA Specialist to join their large-scale CAPEX project based near Copenhagen. This is a fantastic opportunity for a professional in the life sciences sector to advancing their career within a globally recognised pharmaceutical environment.

What you’ll do:

• Review and approve batch records
• QA Review Activities - Perform timely and thorough QA review of QC laboratory documentation, manufacturing batch records, test results, and associated GMP records.
• Deviation Management - Write, review, and approve deviations; ensure strong root cause analysis and effective CAPA implementation.
• GMP Oversight - Provide QA support to QC and DSM operations, ensuring compliance with cGMP, internal procedures, and regulatory expectations.

What you’ll need:

• Extensive QA or Quality Systems experience in a GMP-regulated pharma/biotech environment.
• Demonstrated expertise in writing, investigating, and approving deviations, including strong root cause analysis skills.
• Proficiency with eQMS and ERP systems such as Veeva, TrackWise, SAP, and MS Office/365.

Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!

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