Batch record reviewer m​/f​/d

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).