Expert assurance Offres d'emploi - Corsier-sur-Vevey, VD

In this role, you will be responsible for developing technical solutions, optimizing the Manufacturing platform, and integrating new molecules. You will act as a catalyst and facilitator for organizational and operational initiatives related to efficiency, productivity, reliability (obsolescence, technology watch), compliance, cost and energy considerations. This is an excellent opportunity to oversee a wide variety of manufacturing techniques, including fed-batch, intensified, and continuous processes across different manufacturing suites and products (commercial and clinical). Key Responsibilities : Lead and / or participate in cross-functional projects and task forces, such as tech transfer of new molecules, implementation of new technology, continuous improvement, and major non-conformity investigations.Identify opportunities, build business cases, and promote the deployment of new technology.Ensure complete adoption of changes in the field in a tactful and diligent manner, monitor effectiveness, and ensure compliance with EHS and cGMP requirements (including management of change controls, corrective & preventive actions in the QMS system, and writing and / or reviewing project charters, risk analysis, protocols, and reports as appropriate).Participate in the evaluation of internal and external new molecules on the manufacturing platform.Foster harmonization, synergies, and ensure consistency between different production units.Act as a subject matter expert during internal and external audits and present report-outs to stakeholders and senior management. Your Profile : Strong knowledge and interest in biotechnological processes (preferably USP), detailed manufacturing operations (including automated & execution systems, engineering designs, P&ID, etc.), and new technologies.Ability to manage priorities in a fast-paced environment, fostering pragmatic, solution-oriented, and resilient approaches.Appetite for working cross-functionally, demonstrated leadership in a matrix configuration.Ability to describe complex technical processes or problems in simplified explanations adapted to different audiences.Excellent communication skills, both written and oral. Fluency in French and an excellent command of English.Master’s degree in Biotechnology with 3-5 years of experience within a cGMP biopharmaceutical environment (manufacturing, MSAT, or development functions) ideally.If you are passionate about innovation, have strong leadership skills, and thrive in a team-based culture, we encourage you to apply for this exciting opportunity.