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

veröffentlicht
Kontakt
Thomas Hellmüller, Randstad Inhouse Services Lonza Visp
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Visp, Wallis
Sektor
Bau
Jobtyp
Temporär
Referenznummer
142523-751
Kontakt
Thomas Hellmüller, Randstad Inhouse Services Lonza Visp
Telefon
079 309 99 71

Stellenbeschreibung

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

Qualifikation

  • 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