Junior QA Batch Record Reviewer | Hybrid & Training

Capgemini; Opfikon; Hybrid; CHF 60,000 - 85,000; Full time

Benefits offered by this job

5 weeks vacation

Employee referral bonus

Company shares program

Annual fitness subscription

Job summary

Capgemini Engineering seeks a Junior QA Batch Record Reviewer for a client site in Visp, Switzerland. The role focuses on timely, independent review of electronic batch records in MES Syncade, ensuring records are complete and QA-ready, and coordinating with Manufacturing and Quality teams.

The ideal candidate has GDP/GMP pharma experience, strong communication skills, and a structured, solution-oriented approach. Hybrid work and extensive training opportunities are offered.

Qualifications

• Experience in GDP and GMP regulated pharmaceutical/API industry.
• Experience in batch record review (preferred eBR) or in manufacturing is required.
• Ability to identify non-compliance and gaps from quality standards.
• Very good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation.
• Agile, highly motivated and dynamic drive.

Responsibilities

• Perform timely and independent review of executed electronic batch records (eBRs) in MES Syncade.
• Ensure operations batch records are accurately executed, complete, and ready for QA review.
• Collaborate with Manufacturing and Quality teams to clarify and resolve documentation issues.
• Initiate and support the management of Quality Records (CAPAs and Deviations) for Batch Record review related observations.
• Support preparation of documentation package to enable fast release by QA.

Skills

GDP/GMP experience

Communication skills

Team orientation

Agile mindset

Tools

eBR review

MES Syncade

Job description

Capgemini Engineering seeks a Junior QA Batch Record Reviewer for a client site in Visp, Switzerland. The role focuses on timely, independent review of electronic batch records in MES Syncade, ensuring records are complete and QA-ready, and coordinating with Manufacturing and Quality teams.

The ideal candidate has GDP/GMP pharma experience, strong communication skills, and a structured, solution-oriented approach. Hybrid work and extensive training opportunities are offered.