In this position, you will play a key role in ensuring that manufacturing batches meet all procedural and regulatory expectations. You will review executed batch records, verify documentation completeness, and align with quality standards. This role requires strong attention to detail, the ability to work independently, and a solid understanding of manufacturing processes within a regulated environment.

Start Date: 01/01/2026

Duration: 9 Months

Place of Work: Visp

Key Responsibilities

  • Review executed batch records including production documentation and raw data
  • Ensure full and accurate documentation to support batch release
  • Clarify record comments with operational teams and assess with the responsible QA Manager
  • Support the initiation of deviations and investigations related to record-review findings

Job ID 18408

Candidate Profile

  • Academic background or relevant work experience in Biology, Chemistry, Biotechnology, or a related field
  • Experience in GMP-regulated pharma or API manufacturing is an advantage
  • Ability to identify gaps or non-compliance with quality standards
  • Structured, precise, and well-organized working style; open to new ideas, agile, and highly motivated
  • Fluent English; German language skills preferred