Project Engineer – Black / Clean Utilities
View: 155
Update day: 24-04-2024
Category: High Technology Mechanical / Technical Electrical / Electronics Consulting / Customer Service Executive management
Industry: Medical Equipment Manufacturing Biotechnology Research Pharmaceutical Manufacturing
Position: Mid-Senior level
Job type: Full-time
Job content
Responsibilities
- Own, manage and deliver clean and black utility systems for Biopharmaceutical Facilities as project lead engineer during design, procurement, project execution and turn-over to operations
- Leading and guiding engineering partners, EPCMV contractors and equipment suppliers during the design and execution of CAPEX projects
- Interfacing and communicating effectively with stakeholders being involved such as project / design management, other discipline leads, MSAT, Operations & Maintenance Group, EHS, Qualification and QA
- Collaboration with all parties involved for tasks such as equipment and systems design, specification generation, tendering, expediting, FATs, SATs, commissioning, qualification and start up
- Reporting and providing input of status and forecast of utilities on cost and schedule
- Hands-on involvement in the creation and development of engineering documents and test plans
- Overseeing, aligning and reviewing of engineering documents created by the EPCMV contractor
- Contributing and representing the engineering group at HAZOP and GMP risk analysis
- Performing reviews of vendor design deliverables, scope of work, constructability, and schedule
Requirements
- More than 10 years of experience in an engineering environment and more than 5 years of experience in design engineering throughout phases from feasibility to detail design
- Must have record of accomplishment of on-site project engineering within the life science industry and successful design of clean / black utility systems for biopharmaceutical production facilities
- Experience in GMP environment and knowledge of pharmaceutical standard regulations and guidelines (ISPE, EU GMP Guidelines, ASME, CFR, etc.)
- Organized and structured attention to details, quality and safety in design with excellent documentation skills
- Fluency in English
Deadline: 08-06-2024
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