Project Engineer (f/m/d)

☞ Lonza

전망: 155

갱신일: 26-11-2025

위치: Verviers Liège

범주: 첨단 기술 IT-소프트웨어

산업: Biotechnology Research

수평: Entry level

직업 종류: Full-time

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작업 내용

Belgium, VerviersToday, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.In our Site in Verviers, Belgium | Lonza we are looking for a Project engineer who will be responsible to ensure all critical GMP regarding equipment, facility and/or systems are designed din accordance to GMP, validated and maintained in compliance with user requirements, process parameters and global regulatory guidelines. The specialist works closely with Operations, Quality Assurance, our clientele, and regulatory bodies with scientifically sound, documented evidence that our systems and processes will perform as required so they can be assured of a quality, compliant manufacturing environment. At this level the specialist must possess a full grasp of the duties of Engineering / Validation and is a resource to less experienced members.Key Responsibilities
  • Ensure the CAPEX projects management of Equipment, Utilities, HVAC and Building in a Pharmaceutical sector
  • Take the ownership of all phases or steps included in a project: URS, feasibility, concept, basic & detail Design, budget, timeline, schedule, coordination as well as execution, qualification (FAT, SAT, IOQ, PQ), commissioning, training, start-up and management of validation interfacing
  • Take the lead during the shutdown period and control the work performed
  • Adapt the execution of the shutdown planning in function of issues, delays for delivery or sub-contractors.
  • Manage, complete & check the completion of Change Request Tasks, CAPAs, Deviation & EHS Corrective Actions
  • Offer a great autonomy of work but able to work in a perfect collaboration with a team of engineers
Key Requirements
  • Degree in Engineering (ideally Electro-Mechanics) or equivalent work experience
  • Extensive knowledge and experience in all technical disciplines regarding the project in the pharmaceutical factory
  • Experience handling multiple projects (3-5) simultaneously, keeping track of costs and schedule and ensuring compliance with quality and safety standards.
  • Experience in the field of CSV (Computer System Validation)
  • Experience with SAP, Document Management System preferred
  • Fluent in French and English
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.Reference: R48584Apply
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마감 시간: 10-01-2026

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