QA Documentation Specialist / Batch Record Reviewer (7067)

CTC Resourcing Solutions; Wallis; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

CTC Resourcing Solutions is seeking a QA Documentation Specialist (German-speaking) for a contract role in Valais, Switzerland. The position is on-site and aims to review batch records and monitor critical metrics to ensure timely batch release. Fluency in German is mandatory, English preferred, with GMP experience and a scientific degree as prerequisites.

The contract runs until end-2026 with an option for extension. Suitable candidates will hold a valid Swiss/EU residency or permit.

Qualifikationen

• Bachelor’s or Master’s degree in a relevant scientific field (Pharma/Chemistry/Biotech) or equivalent experience.
• GMP experience in a production environment (min. 2 years).
• Batch record review experience is highly preferred.
• Proven ability to work in GMP environment and execute SOPs.

Aufgaben

• Review paper-based executed batch records within specified timeframe.
• Track, report and monitor batch record review and related metrics for on-time batch release.
• Raise meetings with Ops observers and escalate issues promptly.

Kenntnisse

German language

English language

Communication skills

Ausbildung

Bachelor's/Master's degree or equivalent

Jobbeschreibung

QA Documentation Specialist / 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.

Main Responsibilities:

• Review paperbased 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)
• Great communication skills
• Business fluent German is a MUST, English preferred