We are seeking a highly detail-oriented Batch Record Reviewer to ensure that manufacturing batches are executed and documented in full compliance with GMP standards and internal procedures. The ideal candidate brings strong analytical skills, a solid understanding of pharmaceutical or biotech manufacturing processes, and the ability to work independently in a fast-paced, paper-based documentation environment.
Type of employment: Payroll
Skills: Batch record review
Project start: 02.03.2026
Tasks:
* Review executed paper-based batch records within defined timelines to support on-time batch release.
* Verify accuracy, completeness, and GMP compliance of all manufacturing documentation.
* Track, monitor, and report critical metrics related to batch record review and release readiness.
* Identify deviations, inconsistencies, or documentation gaps and escale observations promptly.
* Initiate and lead discussions with Operations to clarify issues and ensure timely resolution.
* Collaborate closely with Quality Assurance, Production, and other cross-functional teams.
Qualifications:
* Professional experience in a GMP-regulated production environment (minimum 2 years).
* Strong understanding of quality procedures, SOPs, and manufacturing processes.
* Experience in batch record review is highly preferred.
* Bachelor’s or Master’s degree in:Pharmaceutical / Technology / Biotechnology / Chemistry / Pharmacy / or another relevant scientific field
* Excellent attention to detail, accuracy, and organizational skills.
* Strong communication skills and ability to work independently.
* Business fluent German
* Comfortable working with paper-based documentation systems.
* On-site presence in Visp (no home office).
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