Project Engineer
il y a 3 jours
Évreux
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2,000 employees across Europe, Asia, and the Americas. Due to our constant growth, we are looking for a Project Engineer – Secondary Works (Pharma & Non-Pharma) to support our projects at a pharmaceutical manufacturing site in Evreux, France. Your Responsibilities As a Project Engineer – Secondary Works, you will be responsible for the management, coordination, and execution of secondary works (pharmaceutical and non-pharmaceutical) in compliance with GMP and local regulations. Your main responsibilities include: • Acting as the interface with the Engineering Design Office (MOE) during detailed design, construction, and up to mechanical completion and commissioning, • Collecting and consolidating all required data for detailed engineering studies, • Reviewing, controlling, and monitoring detailed design deliverables from contracted companies, • Coordinating and leading the Secondary Works package (pharma & non-pharma) internally with teams and externally with engineering partners, • Managing and supervising subcontractors and external companies on site, • Monitoring construction execution schedules and proactively anticipating deviations, • Tracking and controlling project costs for contracted companies, • Ensuring alignment between costs, schedule, and quality of deliverables in accordance with tender requirements, • Performing commissioning and qualification activities for the concerned packages in collaboration with the dedicated C&Q team, • Ensuring compliance with:, • Good Manufacturing Practices (GMP), • Site procedures and instructions, • Health and safety rules, • French regulations, laws, and decrees in force About You • Minimum 15 years of experience in secondary works within the pharmaceutical industry, • Strong experience with cleanrooms (CNC / Grade D / Grade C) including:, • Floors, partitions, ceilings, doors, and accessories, • Design, construction, commissioning, and qualification phases, • Proven experience in:, • Pharmaceutical changing rooms, • Offices and ancillary areas within pharmaceutical production buildings, • Experience acting as Design Lead for Secondary Works, serving as the single point of contact between the site project team and engineering departments, • Experience working in ATEX zones, • Experience on Seveso-classified sites is a strong plus, • Fluent English is mandatory (French required for site coordination), • Strong organizational, coordination, and stakeholder management skills, • Ability to work in regulated, high-compliance industrial environments Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there is a positive outcome, a technical interview with the Hiring Manager will be arranged. Following a positive technical interview, the recruiter will contact you to discuss next steps and our proposal. If the outcome is negative, you will be informed accordingly and the recruitment process will be closed. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group offers the opportunity to work on international projects, continuously develop your skills, and collaborate with colleagues from all over the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step toward an amazing future with us.