QA Batch Record Reviewer (7067)

CTC Resourcing Solutions; Wallis; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

CTC Resourcing Solutions is assisting a client in Valais, Switzerland to find a German-speaking QA Documentation Specialist on-site for a contract until end-2026 with extension option. The role requires careful batch record review to ensure regulatory and procedural compliance, with strong attention to detail and independence.

Ideal candidates hold a science degree (Pharma/Biotech/Chemistry/Pharmacy) and GMP experience.

Qualifikationen

• German language proficiency required; English preferred.
• Experience in GMP production environment and SOP execution.
• Bachelor’s or Master’s degree in Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy or related science.

Aufgaben

• Review batch records for compliance within the required timeframe.
• Track, report and monitor batch record review metrics to ensure on-time release.
• Raise operations-related observations and coordinate meetings as needed.

Kenntnisse

German fluency

Attention to detail

Independent worker

GMP experience

Ausbildung

Bachelor’s/Master’s in Pharma/Science

Jobbeschreibung

QA Batch Record Reviewer (German-speaking)

Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a QA Documentation Specialist for a contract position till end of 2026 (with option for extension) in Valais area, Switzerland.

This is an on-site position.

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.

Main Responsibilities:

• Review paper based executed batch records within the specified timeframe.
• Track, report and monitor batch record review and other relevant critical metrics to ensure on-time batch release.
• Raise meetings with Ops related observations in a timely manner.

Qualifications and Experience:

• Relevant working/residency permit or Swiss/EU-Citizenship required
• Professional experience in GMP production environment, quality procedures and SOP execution
• Bachelor’s/Master’s Degree or equivalent experience.
• Preferred area of study: Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy or equivalent scientific degree.
• Experience in batch record review is highly preferred.
• GMP experience (min. 2 years)
• Business fluent German is a MUST, English preferred