Engineer / F/H/XLAPORTE Euro is the European subsidiary of Laporte & Associés, a Canadian company with over 500 employees, specializing in engineering for the pharmaceutical, agri-food, and bioindustrial industries. LAPORTE Euro offers a range of services in the disciplines of processes, clean rooms, utilities, packaging, and compliance with offices in France (Nantes, Paris, Lyon, Pau, and Strasbourg), in Switzerland (Geneva and Vevey), and in Belgium, south of Brussels. LAPORTE Euro enhances its local service for its clients. 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 gender, age, ethnic origin, 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 established a fair and equitable recruitment process to ensure equal opportunities for all processes, which takes place in several stages:- Pre-interview via Teams with HR team- Second technical interview with the agency manager- Third interview with managementWe are committed to providing feedback to each of you. When you join our teams, you will benefit from a comprehensive onboarding process from your arrival to the entire interview and evaluation process. We invite you to learn more about our company by visiting our website and following us on LinkedIn for our latest updates!Job Description for the Responsible / you will evolve within a rapidly developing company, in a friendly work atmosphere and different phases of the project. Thanks to your expertise, you will provide technical solutions in compliance with applicable standards and will have the following responsibilities:- Define and implement Master Plans and protocols, and justify critical points to check in a process through criticality analysis tools, manage non-conformities and their follow-up.- Ensure project management on documentation related to the protocols (Writing, Execution of protocols, reports): VMP, AC, QC, QI, QO, QP.- Plan and monitor the activities of on-site tests of QI QO as well as support to QP, cleaning, and possibly to the constructor and client.- Possibly participate in calibration phases of instruments and drafting calibration protocols and metrology associated with the systems (review of protocols and test sheets, monitoring the execution of tests) 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 corporate culture allows you to evolve in an environment that fosters personal and professional growth.The profile we are looking for:- Higher-level engineer with a degree in chemical, pharmaceutical, or biotechnological engineering, you have 3 to 5 years of experience in 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), and pharmaceutical regulations.- You are mobile in Switzerland, with regular travel to our clients' sites.- Proficiency in professional English.All our offers are open to people with disabilities. What we offer:- 2 days of remote work/week according to arrangements- Transportation costs reimbursed up to 100 CHF/month- Our 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 fitness centers are also established in the industrial zone. It is located 5 minutes from the Bardonnex border. jid71e9711aen jit0414aen jpiy26aen