QA Batch Record Reviewer (7067)

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

Zusammenfassung

CTC Resourcing Solutions seeks a QA Batch Record Reviewer (German-speaking) for a contract in Valais, Switzerland. You will review batch records to ensure compliance with GMP, quality procedures and SOPs; this role is on-site and through end of 2026 with extension option.

The ideal candidate holds a Bachelor's or Master's in Pharmaceutical fields, fluent German (English preferred), and strong attention to detail with GMP experience.

Qualifikationen

• 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

Aufgaben

• 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

Kenntnisse

German language

English language

Ausbildung

Bachelor’s/Master’s Degree in Pharmaceutical Sciences

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