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- 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-basedOn 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
- Are you the person who actually enjoys the adrenaline of a surprise inspection? Do you find the "missing link" in a paper trail before anyone else even realizes it’s gone?Our client, a Randstad client, is looking for a Senior QMS & Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece.If you can stare down aAre you the person who actually enjoys the adrenaline of a surprise inspection? Do you find the "missing link" in a paper trail before anyone else even realizes it’s gone?Our client, a Randstad client, is looking for a Senior QMS & Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece.If you can stare down a
- Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventiveTitle: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive
