Looking to step into a new pivotal role within a global CMO? Ready to help shape the future of healthcare manufacturing?

Proclinical is seeking a detail-oriented and motivated individual to join as a QA Batch Record Reviewer. In this role, you will ensure that manufacturing processes comply with established procedures and regulatory requirements. You will play a key role in supporting batch release by reviewing executed batch records and collaborating with the operations and quality assurance teams.

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:

• Evaluate batch records, including production documentation and raw data.
• Ensure completeness and accuracy of documentation packages to support batch release.
• Address comments or discrepancies in batch records by clarifying with the operations team and consulting with the QA Manager.
• Assist in initiating deviations and investigations related to batch record observations.

Key Skills and Requirements:

• Academic background or relevant experience in Biology, Chemistry, Biotechnology, or a related field.
• Familiarity with GMP-regulated pharmaceutical or API industries is advantageous.
• Strong ability to identify non-compliance and quality gaps.
• Organized, precise, and open to new ideas with a proactive and dynamic approach.
• Fluent in English (written and verbal); German language skills are a plus.
  

If you are having difficulty in applying or if you have any questions, please contact Ashley Benentt 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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