QA Batch Review Specialist at Visp

Details of the job offer

  2026-10-21
  Full time
  Temporary
Gi Group co-branding

QA Specialist - Batch Record Reviewer


Location: Valais, Switzerland (Onsite)

Contract: 6-Month Fixed-Term Contract

Start Date: Immediate


About the Role

We are currently seeking a Batch Record Reviewer to join a leading pharmaceutical manufacturing environment in Visp. This position is ideal for a detail-oriented professional with experience in GMP-regulated manufacturing or batch record review who is available to start immediately.

Working closely with Manufacturing and Quality teams, you will ensure the accuracy, completeness, and compliance of electronic batch records, supporting efficient batch release activities and overall quality compliance.


Key Responsibilities

  • Perform timely and independent review of executed electronic batch records (eBRs) within MES Syncade.
  • Ensure batch records are accurately completed, compliant, and ready for QA review.
  • Identify documentation discrepancies, compliance gaps, and quality-related issues.
  • Collaborate with Manufacturing, Operations, and Quality teams to investigate and resolve documentation observations.
  • Initiate and support the management of Deviations and CAPAs related to batch record review findings.
  • Support the preparation of documentation packages to facilitate timely QA batch release.
  • Ensure compliance with GMP and GDP requirements throughout the review process.
  • Contribute to continuous improvement initiatives focused on documentation quality and operational excellence.


Required Qualifications

  • Previous experience in a GMP and/or GDP-regulated pharmaceutical, biotechnology, or API manufacturing environment.
  • Experience in Batch Record Review (preferably electronic batch records) or within GMP Manufacturing Operations.
  • Strong understanding of GMP documentation requirements, deviations, CAPAs, and compliance processes.
  • Ability to identify non-compliance issues and documentation gaps against quality standards.
  • Experience with MES systems, ideally Syncade, is highly desirable.
  • Fluent in English (written and spoken).
  • German is a strong advantage.



  Pharmaceutical and biotechnology
  Pharmaceutical and biotechnology
  17388
  Wallis - Visp - Visp

Contact now

Bouchelil Thama
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CONTACT NOW
thama.bouchelil@gigroup.com

QA Batch Review Specialist
Temporary / Visp
Place of work - City:
Visp
Industrial sector:
Pharmaceutical and biotechnology
Professional area:
Pharmaceutical and biotechnology
Number of vacancies:
5
Reference code:
24338
Salary per:
Job offer insertion date:
2026-10-21

QA Specialist - Batch Record Reviewer


Location: Valais, Switzerland (Onsite)

Contract: 6-Month Fixed-Term Contract

Start Date: Immediate


About the Role

We are currently seeking a Batch Record Reviewer to join a leading pharmaceutical manufacturing environment in Visp. This position is ideal for a detail-oriented professional with experience in GMP-regulated manufacturing or batch record review who is available to start immediately.

Working closely with Manufacturing and Quality teams, you will ensure the accuracy, completeness, and compliance of electronic batch records, supporting efficient batch release activities and overall quality compliance.


Key Responsibilities

  • Perform timely and independent review of executed electronic batch records (eBRs) within MES Syncade.
  • Ensure batch records are accurately completed, compliant, and ready for QA review.
  • Identify documentation discrepancies, compliance gaps, and quality-related issues.
  • Collaborate with Manufacturing, Operations, and Quality teams to investigate and resolve documentation observations.
  • Initiate and support the management of Deviations and CAPAs related to batch record review findings.
  • Support the preparation of documentation packages to facilitate timely QA batch release.
  • Ensure compliance with GMP and GDP requirements throughout the review process.
  • Contribute to continuous improvement initiatives focused on documentation quality and operational excellence.


Required Qualifications

  • Previous experience in a GMP and/or GDP-regulated pharmaceutical, biotechnology, or API manufacturing environment.
  • Experience in Batch Record Review (preferably electronic batch records) or within GMP Manufacturing Operations.
  • Strong understanding of GMP documentation requirements, deviations, CAPAs, and compliance processes.
  • Ability to identify non-compliance issues and documentation gaps against quality standards.
  • Experience with MES systems, ideally Syncade, is highly desirable.
  • Fluent in English (written and spoken).
  • German is a strong advantage.



Call us now to book an interview.

Bouchelil Thama
thama.bouchelil@gigroup.com

https://ch.gigroup.com/job-offer-detail/visp-qa-batch-review-specialist/24338/