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Clean Utilities Engineer for biopharmaceutical facilities (long term contract)

Ref: JN-062021-182540

Publié le 26 July 2021
Location
Valais
Catégorie
Ingénierie & production

This is a very exciting long term Modis project role a very exposed life sciences company in the beautiful Swiss-Valais area. You have the chance to make an impact on the forefront of life sciences engineering, whilst you live in a very beautiful landscape.

• Project Engineering for clean utility systems for biopharmaceutical facilities

• Leading and guiding engineering partners, contractors and equipment suppliers during the design and execution of projects within the site

• Interfacing and communicating effectively with stakeholders being involved such as project / design management, other discipline leads

• Collaboration with all parties involved for tasks such as equipment and systems design, specification generation, tendering, expediting

• 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 contractor.

• Making sure that 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 risk analysis.

• Ensuring incorporation of lesson learnt and required changes into design.

• Performing reviews of vendor design deliverables, scope of work, constructability, and schedule.

• Track record of on-site project engineering within the life science industry / high technology sector,

• 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

• 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.

• English fluent / German basics are a nice to have