Senior QA Specialist Small MoleculesOn behalf of one of our clients, a fast-growing pharmaceutical company based in the canton of Vaud, we are looking for a Senior Quality Assurance Specialist – Small Molecules.Temporary mission until the end of the year, with the possibility of a role.You are responsible for the quality supervision of activities and controls carried out at subcontractors (CMOs) for a portfolio of products (raw materials, active substance, finished product).You act as a true QA reference throughout the product life cycle, ensuring compliance with cGMP requirements and regulatory files.Your responsibilities- Ensure quality supervision of CMOs (compliance, performance, action plans)- Manage QA activities throughout the product life cycle: development, transfers, registration- Manage quality events: OOS, CAPA, change controls- Participate in the qualification of CMOs and the management of Quality Agreements- Review and approve quality records (specifications, monographs, stability data)- Contribute to batch release decisions- Manage APQRs and ensure follow-up of quality indicators- Support interactions with health authorities- Ensure preparation for inspections and maintain a high level of GMP compliance- Actively contribute to continuous improvement (Lean, QA performance)Your profile- Scientific degree (Master or PhD – pharmacy, chemistry, biotechnology, engineering)- Minimum 5–6 years of experience in Quality Assurance in the pharmaceutical industry- Expertise in Small Molecules (ideally semi-solid products)- Confirmed experience in QA oversight of CMOs- Very good command of cGMP and regulatory requirements- Proficiency in drafting quality documents (APQR, SOPs)- High level of project management and technical transfer skills- Excellent communication and negotiation skills- Fluent English is essential- Availability for travel (up to 20%) jidc44f483aen jit0520aen jpiy26aen