QA Documentation Specialist

MANPOWER AG – Your career, our focus!

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ManpowerGroup is the world's leading company for workforce solutions.
With our three brands – Manpower, Experis, and Talent Solutions – we support companies from various industries with their recruitment needs. For 75 years, we have been operating in over 75 countries and accompany our clients throughout Switzerland to successfully carry out their tasks and projects.

Purpose of the Role Responsible for reviewing executed paper-based batch records to ensure manufacturing activities were performed according to GMP procedures, internal SOPs, and regulatory requirements. The role requires strong attention to detail, independence, and a solid understanding of pharmaceutical manufacturing processes.

• Review executed paper-based batch records within agreed timelines.
• Verify compliance with GMP requirements, SOPs, and manufacturing procedures.
• Track, monitor, and report batch review progress and critical release metrics.
• Support on-time batch release activities.
• Identify observations/deviations and raise them with Operations in a timely manner.
• Participate in discussions and meetings related to batch documentation findings.

• Bachelor's or Master's degree in:
  • Pharmaceutical Technology
  • Biotechnology
  • Chemistry
  • Pharmacy
  • Or another relevant scientific discipline
• Equivalent industry experience may be considered.

• Minimum 2 years of GMP experience in a pharmaceutical or biotech manufacturing environment.
• Experience with quality procedures and SOP execution.
• Batch Record Review experience is highly preferred.
• Knowledge of pharmaceutical manufacturing documentation and compliance requirements.

• Strong attention to detail.
• Ability to work independently.
• Excellent communication and stakeholder management skills.
• Strong understanding of GMP regulations and documentation practices.

• Business-fluent German (mandatory)
• English preferred.

• 100% On-Site in Visp
• No home office / remote work option.
• Paper-based documentation environment.

A GMP professional with pharmaceutical manufacturing experience who has hands-on exposure to batch record review, is highly detail-oriented, fluent in German, and capable of managing documentation review timelines to support compliant and timely batch release.