On-Site Batch Record Reviewer (GMP/GDP) – Valais

CTC Resourcing Solutions AG; Wallis; Sur place; CHF 62 000 - 96 000; Plein temps

Résumé du poste

CTC Resourcing Solutions AG and our client seek a Batch Record Reviewer for an on-site 7-month contract in the Valais region of Switzerland. The role focuses on independent review of executed electronic batch records (eBRs) in MES Syncade and ensuring records are complete for QA.

The ideal candidate has GDP/GMP experience in pharma, strong quality focus, excellent communication, and the ability to work under pressure in a collaborative environment.

Qualifications

• Swiss/EU citizenship or valid work permit required.
• 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.
• Structured, focused and well-organized working attitude.
• Open-minded for new ideas and suggestions; solution-oriented.
• Agile, highly motivated and dynamic drive.
• Ability to produce reliable results under stress.

Responsabilités

• Perform timely and independent review of executed electronic batch records (eBRs) in MES Syncade.
• Ensures that 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 in 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.

Connaissances

Batch record review

GDP/GMP experience

eBR experience

Communication skills

Quality compliance

Outils

MES Syncade

Description du poste

CTC Resourcing Solutions AG and our client seek a Batch Record Reviewer for an on-site 7-month contract in the Valais region of Switzerland. The role focuses on independent review of executed electronic batch records (eBRs) in MES Syncade and ensuring records are complete for QA.

The ideal candidate has GDP/GMP experience in pharma, strong quality focus, excellent communication, and the ability to work under pressure in a collaborative environment.