Quality Assurance Specialist - Manufacturing - Permanent position - 100%

• 06 août 2026 • 100% • Temporary • 1201 Genève • Log in to see the jobup.ch salary estimate Recognized and essential for over 40 years, Multi Personnel is an agency specialized in the provision of administrative and management personnel, temporary and permanent, in many economic sectors, such as banking, financial companies, multinationals, NGOs, SMEs, and local institutions. We wish to recruit a Quality Assurance Specialist - Manufacturing - Permanent position - 100% Responsibilities: ## • Ensure that activities related to production quality comply with company policies and Corporate Quality directives. Main contact in case of production deviation, • Lead and manage deviations, including those related to production, maintenance, packaging, and laboratory activities, by conducting and coordinating investigations in collaboration with the relevant functions, • Define, implement, and monitor corrective and preventive actions (CAPA) within the scope of responsibility, ensuring timely execution and effectiveness in accordance with defined deadlines, • Manage complaint investigations, • Participate in the review and approval of validation/qualification documentation related to the production area, • Ensure the timely creation, review, and update of QA operations documents, • Review/approve for issuance GMP documents related to the production area (SOP, specifications, protocols, reports..), • Participate in and/or lead risk analyses, in collaboration with cross-functional teams, • Participate in the change management process, • Auditor during self-inspections and external audits (lead auditor if qualified), • Support external audits, Notified Bodies, and Regulatory Authorities, • Review audit trails of GMP systems. • Training for classified areas • Review of production batch records • Release of incoming consumables • Review of packaging batch records • Promptly report any quality alerts or problems to the Quality Operations Manager and the Quality Unit Manager and actively contribute to the resolution of significant quality problems. • Ensure effective communication and collaboration with Production, Maintenance, Packaging, and other relevant functions to support product quality throughout its lifecycle *Management* • Indirect management of investigation teams. Profile: ## • University degree in Pharmacy, Chemistry, or Biochemistry • Minimum 5 years in quality management in the pharmaceutical industry, on a manufacturing site • Solid knowledge of cGMP, including Annex 1 • Experience in lyophilized products and aseptic processing • Indirect management in projects or investigations • Quality commitment, flexibility, initiative, and problem-solving skills. • Excellent team spirit with strong communication skills. • Mandatory proficiency in French and English Your contact person: ## Your contact for this position is Leila. With over 15 years of experience in the recruitment field, he/she will know how to accompany you, advise you, and provide answers to all your questions regarding the position. This job does not quite match what you are looking for but our values speak to you? Do not hesitate to send us your spontaneous application! *We will only respond to applications whose profile matches the requested description.*