Chargé Qualité Produit

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, ACO®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to a blended-branded business to win in self-care. **Description générale**: The Chargé Qualité Produit covers transversal activities related to Quality Assurance for a combination of Medical Devices, Cosmetic and General products: - Product complaint management. - Batch release activities. - Support to trending activities. - Support to QMS activities. **Périmètre du poste**: Product complaint management. You dispatch, follow-up and close complaints in a timely manner as per internal procedure, build a relationship with all stakeholders involved in the complaint flow and ensure mutual support. You support process improvement initiatives and harmonization activities. You are responsible for batch release activities and for the timely release of batches to meet the needs of the business while ensuring that all quality aspects are covered. In this position, you will become proficient in the use of the ERP system and coordinate the release of products under quarantine following internal procedures. The job includes the preparation and monitoring of reports and trend analysis. You own sections of the monthly complaint analysis and provide inputs in preparation of the management review. Support quality activities performed at Perrigo. You actively participate in the maintenance of the QMS and in NB audits and support the team with the creation and revision of quality documents, coordinate rework/relabeling activities, support the handling of quality processes (CAPA, Deviations, Non-Conformities ). Within the ISO13485:216 certification scope of HRA Pharma, you are the backup of the “Subcontracted Production Control” Process owner for piloting the process, handling periodic KPI review and follow-up analysis. **Expérience requise**: - Master degree with a scientific background, with 2-3 years of experience in a pharmaceutical or medical devices company - 2-3 years experience within quality assurance - Fluency in French and Operational English is necessary - Good knowledge of ISO13485 and GMP processes - IT proficient, SAP knowledge of advantage **Benefits** We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more about Total Rewards at Perrigo. **Hybrid Working Approach** We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles. We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. Our full Equal Employment Opportunity and Affirmative Action Policy Statement is available on our main career site in English and Spanish and will be provided in other accessible forms for persons with disabilities. #DIV #weareperrigo