Batch Record Reviewer

Work Setup: Fully on-site (paper-based documentation; no remote option)

Summary

We are seeking a detail-oriented Batch Record Reviewer to support GMP manufacturing operations on a 3-month on-site contract in Visp. In this role, you will ensure that executed batch records are reviewed accurately and in full compliance with internal procedures and regulatory requirements.

The ideal candidate has strong experience in GMP environments, excellent attention to detail, and the ability to work independently while collaborating effectively with Operations and Quality teams.

Key Responsibilities

• Review paper-based executed batch records within defined timelines.
• Ensure all documentation complies with GMP standards, internal procedures, and regulatory requirements.
• Identify documentation discrepancies, deviations, or inconsistencies and elevate appropriately.
• Track, monitor, and report batch record review status and key performance indicators to ensure timely batch release.
• Organize and lead meetings with Operations to address observations and resolve documentation issues promptly.
• Contribute to continuous improvement of review processes and quality standards.

Requirements

Education & Experience

• Bachelor’s or Master’s degree in Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy, or a related scientific discipline — or equivalent professional experience.
• Minimum 2 years of experience in a GMP-regulated production environment.
• Strong knowledge of quality procedures and SOP execution.
• Proven experience in batch record review is highly preferred.
• Exceptional attention to detail and accuracy.
• Ability to work independently and manage deadlines effectively.
• Strong understanding of manufacturing processes within a pharmaceutical or biotech environment.
• Excellent communication and stakeholder coordination skills.
• Business-fluent German (mandatory).

Interested? Apply now or send your CV to

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