Project Engineer Clean and Process Utilities m/f 100% in Visp

Thomas Hellmüller, Randstad Inhouse Services Lonza Visp
jetzt bewerben

job details

Visp, Wallis
Thomas Hellmüller, Randstad Inhouse Services Lonza Visp
079 309 99 71


On behalf of Lonza AG in Visp, we are looking for a project manager for a temporary assignment for 18 to 24 months from January 1st, 2021.

Roles & 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 Lonza 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 lessons 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

  • Languages: German and English

  • University degree in process, mechanical engineering or equal