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レベル: Entry level
ジョブタイプ: Full-time
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仕事内容
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
- 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
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締切: 10-01-2026
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