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 preventive
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 preventive
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
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 a
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 a
For our client, an international company based in Visp, we are looking for a Junior Buyer (Capex). The Junior Buyer (Capex) supports the execution of capital expenditure procurement activities within assigned projects and operational buying scopes. This role focuses on operational procurement execution, supplier coordination, and ensuring compliance with procurement processes while working under the guidance of senior procurement leadership to support
For our client, an international company based in Visp, we are looking for a Junior Buyer (Capex). The Junior Buyer (Capex) supports the execution of capital expenditure procurement activities within assigned projects and operational buying scopes. This role focuses on operational procurement execution, supplier coordination, and ensuring compliance with procurement processes while working under the guidance of senior procurement leadership to support
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
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
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