CDI - Production Validation Manager M/F

Vetoquinol has been an independent veterinary pharmaceutical Group for over 90 years. Our fast-growing Group bases its development on the competence and involvement of its teams and on the search for innovative solutions in animal health (new projects are underway, modernization of our equipment and workspaces, a new customer approach, an opening towards biotechnologies…). More than 2500 employees distributed across 24 countries contribute daily to the satisfaction of our main client: the veterinarian. We place People at the heart of our concerns and our corporate strategy and do everything possible on a daily basis to support our Managers, develop agile skills and behaviors, and improve the well-being at work of all our employees. Strong values reflect our transformation today: Trust, Dare, and Collaborate! At Vetoquinol, we want to accomplish more, all together! We invite you now to discover our institutional video: https://player.vimeo.com/video/264055977

Job Summary: Guarantee the completion of initial, periodic, and continuous validations (qualification of equipment, utilities, automated and computerized systems, cleaning, and processes), within your scope of intervention, in a consistent and coherent manner with current regulations (GMP, specific guidelines, and other current standards) and with the strategy and investment projects of the Group industrial and quality management. You will report to the QA Manager of our Autonomous Production Unit - Solid Forms, your main missions as Solid Forms Validation Manager will be the following; Define and implement the validation master plan, integrate regulatory and investment project constraints into it, and operate with a focus on optimizing costs and deadlines. Participate in investment projects related to measuring devices, equipment, automated and computerized systems, utilities, and premises. Define and supervise the project validation cycle and provide the necessary technical and quality expertise. Perform regulatory monitoring in the technical, quality, and validation fields. Manage outsourcing activities in your field, from the definition of needs to the verification and monitoring of service provider deliverables. Supervise, coordinate, and lead your team's activity and ensure the achievement of assigned objectives and the development of their skills. Participate in the preparation and monitoring of budgets for your activity. Ensure the administrative follow-up of your field of activity by keeping associated procedures up to date and providing your expertise on the implemented procedures. Supervise activities related to technical change control and participate in decision-making if necessary. Ensure the safety of people at workstations and implement corrective actions in case of anomalies.

With a Master's degree (Bac+5) in a scientific field, Engineer, or Industrial Pharmacist, you have at least 5 years of experience in a similar position. Knowledge of solid forms will be highly appreciated. Thanks to your technical and quality expertise and your mastery of GMP, you are able to write and approve technical or quality documents. You are rigorous, organized, and have analytical and synthesis skills. You possess managerial skills that allow you to manage a team of employees. Your level of English allows you to communicate easily with various English-speaking interlocutors.

Conditions & benefits: Management position in CDI, based in Lure, available immediately. Base remuneration according to profile, holiday bonus, profit-sharing, participation, and company savings plan. Vetoquinol also offers meal vouchers, RTT, CSE actions, possibility of internal carpooling or 50% reimbursement of public transport subscriptions. Events/actions promoting well-being at work, Training and opportunities for evolution.