.Pre-Clinical Quality ManagerWith a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermo-cosmetics, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ – the skin – meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals.We are looking for a professional to assure the quality and GLP compliance of Pre-Clinical Development activities sponsored by Galderma as well as related processes and systems.Key ResponsibilitiesEstablish the R&D Auditing strategy dedicated to pre-clinical development activities related to Prescription, Aesthetics and Cosmetics Galderma sponsored projects.Define, manage, implement and, as necessary, adapt with R&DQA/Innovation Quality partners the audit program.Conduct internal and external audits.Assure the compliance of pre-clinical development activities with the company outsourcing governance.Contribute to the development and optimization of the Quality Management System dedicated to Pre-Clinical Development.Support regulatory intelligence activities.Provide appropriate training ensuring the buy-in by R&D employees of the quality management system and corresponding regulations and guidelines.Participate in the quality analyses of Galderma first-priority projects to identify any compliance trend that would potentially jeopardize the admissibility of their results by Competent Authorities.Assure international inspection readiness of Galderma R&D activities and coordinate GLP regulatory inspections conducted by Competent Authorities worldwide.Skills & QualificationsEffective experience in R&D activities and Quality Assurance.Robust experience in R&D audits, inspections and development/implementation of Quality Management Systems.Be familiar with R&D IT environment, tools (Documentum platform, Trackwise, Trial Interactive....) and validation approach (GAMP, 21CFR part 11...).Confirmed expertise in Good Laboratory Practices and associated regulations.What we offer in returnYou will be working for an organization that embraces diversity & inclusion and believes we will deliver better outcomes by reflecting the perspectives of our diverse customer base.You will receive a competitive compensation package with bonus structure and extended benefit package.You will be able to work in a hybrid work culture.You will participate in feedback loops, during which a personalized career path will be established.You will be joining a growing company that believes in ownership from day one where everyone is empowered to grow and to take on accountability