Il y a 6 heures
QA Batch Record Reviewer
- 27 février 2026
- 100%
- Temporaire
- allemand (Courant)
- Visp
À propos de cette offre
Jobdescription
On behalf of a client company, we are looking for a QA Batch Record Reviewer to ensure that production batches have been manufactured correctly, in accordance with established procedures and regulatory requirements. The ideal reviewer has great attention to detail, is able to work independently, and possesses a thorough knowledge of the manufacturing process they are reviewing.
Location: On-Site in Visp (no home office) - Dealing with paper-based documentation.
Key Responsibilities
On behalf of a client company, we are looking for a QA Batch Record Reviewer to ensure that production batches have been manufactured correctly, in accordance with established procedures and regulatory requirements. The ideal reviewer has great attention to detail, is able to work independently, and possesses a thorough knowledge of the manufacturing process they are reviewing.
Location: On-Site in Visp (no home office) - Dealing with paper-based documentation.
Key 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 Operations (Ops) related observations in a timely manner.
- Professional experience in a GMP production environment, quality procedures, and SOP execution, and/or a 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 (minimum 2 years).
- Great communication skills.
- Business fluent German is a MUST, English is preferred.
Luciana Sardo
À propos de l'entreprise
Avis
4.7
- Style de management4.5
- Salaire et avantages3.5
- Opportunités de carrière4.0
- Ambiance et conditions de travail4.5
