Engineer / F/H/LAPORTE Euro is the European subsidiary of Laporte & Associés, a Canadian company with over 500 people, specializing in engineering for the pharmaceutical, agri-food, and bio-industrial industries. LAPORTE Euro offers a range of services in the disciplines of processes, clean rooms and utilities, packaging, and compliance, with offices in France (Nantes, Paris, Lyon, Pau, and Strasbourg), Switzerland (Geneva and Vevey), and Belgium, south of Brussels. LAPORTE Euro is intensifying its proximity service for its clientele. As a growing company, LAPORTE Euro is actively committed to diversity and works to create an inclusive work environment where everyone feels valued and respected, regardless of their gender, age, ethnic origins, sexual orientation, gender identity, disability, or any other characteristic that makes us unique. LAPORTE Euro is also committed to a sustainable development policy. LAPORTE Euro has implemented a fair and equitable recruitment process to ensure equal opportunities for all. The process takes place in several stages: - Pre-interview via Teams with the HR team - Second technical interview with the agency manager - Third interview with management. We commit to providing feedback to each candidate. Once you join our teams, you will benefit from a comprehensive onboarding process, including all interviews and reviews. We invite you to learn more about our company by visiting our website and following us on LinkedIn for our latest news! Job Description for the Manager / You will evolve within a growing company, in a friendly work atmosphere, and through different phases of the project. Thanks to your expertise, you will provide technical solutions in compliance with the applicable standards and will have the following responsibilities: Define and implement Master Plans / protocols and justification of critical points to be verified in a process through criticality analysis tools, manage non-conformities and their follow-up. Ensure project documentation related to the (Writing, Execution of protocols, reports): VMP, AC, QC, QI, QO, QP. Plan and ensure the monitoring of field activities such as QI QO tests as well as support for the QP, cleaning, and possibly to the manufacturer and client. Participate in the phases of instrument calibration and writing of calibration and metrology protocols associated with the control of systems (review of protocols and test sheets, monitoring of test execution) which would be complementary. You will be able to continue developing your skills by participating in projects and through mobility within the group, according to opportunities. Our company culture allows you to evolve in an environment that promotes collaboration and growth. The profile we are looking for: - Higher education level in chemical engineering, pharmaceutical or biotechnology, with 3 to 5 years of experience on pharmaceutical, cosmetic industrial projects, or technical knowledge of instruments and certain equipment (autoclave, washer, CIP/SIP) is a plus - Knowledge of Good Manufacturing Practices (GMP/cGMP), regulatory and pharmaceutical standards - You are mobile in Switzerland; regular travel to our clients' sites will be expected - Proficient in professional English All our offers are open to persons with disabilities. What we offer: - 2 days of telecommuting/week subject to conditions - Reimbursement of public transport costs up to 100 CHF/month - The agency is located within a brand-new Business Center, equipped with a cafeteria and an on-site restaurant. Parking spaces are available in the industrial zone, and the site is also accessible by public transport. Numerous shops and gyms are also located in the industrial zone. It is located 5 minutes from the Bardonnex border. jidf7d6960aen jit0414aen jpiy26aen