Quality Assurance Engineer in Geneva

to support leading pharmaceutical projects within a dynamic and highly regulated environment. This role offers the opportunity to contribute to quality assurance and compliance activities across the pharmaceutical product lifecycle, ensuring adherence to GMP standards and regulatory requirements while collaborating with cross-functional international teams.ResponsibilitiesSupport and maintain Quality Management System (QMS) processes in compliance with GMP and applicable regulatory requirements.Manage and contribute to deviation investigations, CAPA implementation, change controls, and risk assessments.Participate in internal and external audits, inspections, and supplier qualification activities.Review and approve quality documentation, including SOPs, protocols, reports, and quality records.Ensure compliance with pharmaceutical regulations, company procedures, and industry best practices.Collaborate with Manufacturing, Engineering, Validation, Regulatory Affairs, and other stakeholders to drive quality initiatives.RequirementsBachelor's or Master's degree in Life Sciences, Pharmacy, Chemistry, Biotechnology, Engineering, or a related field.Minimum 5 years of experience in a Quality role within the Pharmaceutical, Biotechnology, or Life Sciences industry.Strong knowledge of GMP regulations and quality systems.Experience with deviations, CAPA, change control, risk management, and audit processes.Familiarity with international regulatory requirements and quality standards.Professional proficiency in English. #J-18808-Ljbffr