Beschreibung

Process 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, 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), in Switzerland (Geneva and Vevey) and in Belgium, south of Brussels. LAPORTE Euro is intensifying its proximity service for its clients. 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 backgrounds, 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. The process takes place in several stages: - Pre-interview via Teams with the HR team - Second technical interview with the branch manager - Third interview with management. We are committed to providing feedback to each candidate. When you join our teams, you will benefit from a comprehensive onboarding process from your arrival throughout all interviews and assessments. We invite you to learn more about our company by visiting our website and following us on LinkedIn for our latest updates! Job DescriptionAs the Agency Manager of the Geneva agency, you will evolve within a rapidly developing company, in a friendly work environment through different phases of the project (Audit, APS, APD, calls for proposals, monitoring). You will bring your expertise in processes and propose technical solutions while respecting regulatory requirements, deadlines, costs, and the budget defined with the client. Some responsibilities regarding the definition of the need: Identifying client needs and translating them into technical solutions; Definition and development of process flow diagrams; Development of balances (flow rate, pressure loss) and thermal analyses; Preliminary sizing of equipment and instruments necessary for process implementation and defining their parameters and P&IDs; Sizing equipment by performing calculation notes, design studies, and piping routes; Drafting various technical documents adapted to client requests; Launching calls for proposals to suppliers until the order phase by evaluating suppliers from a technical, cost, quality, and planning perspective; Analyzing supplier offers/technical evaluations; Monitoring project documents and phases from the start of work through to completion, including risk analyses and project reviews (HAZOP, FMEA… to QI/QO/QPA). Through this technical work, you will also develop in project management, where quality, scheduling, and budget tracking will be crucial. You will be able to further develop your skills by participating in projects and through mobility within the group, depending on opportunities. Our corporate culture allows you to evolve in an environment that promotes personal development and growth.Profile we are looking for:Higher education at the engineering level in process engineering, biological engineering, or related fields, with at least 5 years of experience related to pharmaceutical processes. Desirable knowledge of Good Manufacturing Practices (GMP), pharmaceutical regulations, and standards. You are mobile in Switzerland, with occasional travel expected to our clients' sites. Proficiency in professional English. Knowledge of clean utilities production and distribution systems (water and gas) would be a plus. All our job offers are open to people with disabilities.What we offer:2 days of remote work per week, transportation costs covered. jid2831ac0aen jit0206aen jpiy26aen