Project Engineer - Clean & Process Utilities

Are you a Project Engineer - Clean and Process Utilities interested in working for one of the most interesting names in High-Tech Biopharmaceuticals?

Are you looking for something new?!

Title: Project Engineer - Clean and Process Utilities

Location: Visp, Switzerland

Rate: Open

Openings: 1 Engineer

Contract/Perm: Contract (12-Months)

A Fantastic new role has just opened up at one of our leading COUNTRY based clients offering the successful candidate the opportunity to join a hard-working team working on exciting projects in the pharmaceutical sector.

Responsibilities:

• Own, manage and deliver clean and process 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 within the Ibex site in Visp.
• 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.
• Making sure that the clients internal standards and requirements are correctly incorporated.
• Ensuring that designs follows good engineering practices, code and standards.
• Organizes, leads and protocols coordination design review workshops and progress meetings
• Contributing and representing the engineering group at HAZOP and GMP risk analysis.
• Ensuring incorporation of lesson learnt and required changes into design.
• Performing reviews of vendor design deliverables, scope of work, constructability, and schedule.
• High proficiency in general technical understanding and in depth knowledge of clean / process and black utility requirements for biopharmaceutical production facilities.
• Comprehensive GMP skills and knowledge of pharmaceutical standard regulations and guidelines (ISPE, EU GMP Guidelines, ASME, CFR, etc.).
• Ability to drive commercial and schedule awareness during all phases of the project cycle.
• Strong analytical thinking.
• Organized and structured attention to details, quality and safety in design with excellent documentation skills.
• Cross culturally aware and adaptable.
• Willing to rise to new challenges and willing to take risks.
• Self-starter, proactive, excellent in problem-solving and communication in a highly agile environment.

Requirements:

• Shall have background in design engineering throughout phases from feasibility to detail design.
• Must have track record of on-site project engineering within the life science industry / high technology sector, incl. start-up and qualification phases.
• Successfully designed clean / process utility systems.
• Significant experience in an engineering environment with focus on execution and projects delivery
• Languages: German and English.
• University degree in process, mechanical engineering or equal

If you are interested, please do not hesitate to email or call me!

S.Hubert@Proclinical.com

DL: +44 203 949 8594

CH: +41 61 508 7073

Mob: +44 7592 053 700