QA Batch Record Reviewer

QA Batch Record Reviewer (m/w/d)

Techfirm industrie AG is looking for support! Are you interested in joining our team operating in the Wallis to work in the pharmaceutical production area? We are looking for a colleague to work on Batch Record Reviewing activities!

Main purpose of this role :

Making sure the batch was made properly, according to procedure and regulatory requirements. Reviewers should have great attention to detail, be able to work independently, and have a thorough knowledge of the manufacturing process they are reviewing.

What you’ll do:

Review of the Executed Batch Records (e.g. production documentation review, raw data etc).

Support batch release by ensuring the completeness of the documentation package.

Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager.

Support the initiation of deviations and investigations for Batch Record review related observations.

What we’re looking for:

Academic degree OR relevant work experience in Biology/Chemistry/Biotechnology or other related field.

Previous experience in GMP regulated pharmaceutical / API industry is an advantage.

Ability to identify non‑compliance and gaps from quality standards.

Structured, precise and well‑organized working attitude; open‑minded for new ideas and suggestions; agile, highly motivated and dynamic drive.

Fluent English (written and verbal) is required, German language skills preferred.

• Work location
  : 3930 Visp (VS)
• Additional information on the place of work
  : 2 days remote working possible after onboarding
• Workload
  : 100%
• Employment start
  : 05.01.2026
• Employment duration
  : 30.09.2026
• Qualification
  : skilled
• Work experience
  :
  More than 1 year
• Education
  :
  Master’s degree from a university of applied sciences or equivalent
• English
  :
  Orally – Very good knowledge, Written – Very good knowledge
• By email
  : g.killig