Pharma Project Engineer & Technical Lead (Contract)

BioTalent

Oberwallis

Vor Ort

CHF 120.000 - 160.000

Vollzeit

14 Tage+

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Zusammenfassung

BioTalent in Switzerland is seeking a Project Engineer / Technical Project Lead to translate requirements into engineering solutions and coordinate multidisciplinary activities across projects. You will review and approve critical documentation and develop P&IDs to ensure project milestones are met.

Role requires GMP experience, hands-on process equipment knowledge, and strong collaboration with vendors and stakeholders to drive successful outcomes in a regulated environment.

Qualifikationen

  • 3–5 years in project engineering or project management.
  • Experience in pharmaceutical, biotech, or chemical industries.
  • Hands-on experience with process equipment in GMP environments.
  • Proven ability to deliver engineering projects.

Aufgaben

  • Translate user requirements into technical engineering solutions.
  • Coordinate multidisciplinary engineering activities across projects.
  • Review and approve engineering documentation (URS, FS, TS, design specs, FAT/SAT, validation reports).
  • Develop and review P&IDs (from design to final status).
  • Support P&ID walkdowns, mechanical completion, and punch list closure.
  • Ensure compliance with the client's standards and GMP regulations.
  • Support commissioning, qualification, and validation activities.
  • Manage external vendors, contractors, and equipment suppliers.
  • Act as a liaison between technical and non-technical stakeholders.
  • Drive project execution and ensure delivery of technical milestones.

Kenntnisse

Project management
Engineering
Stakeholder management

Tools

P&IDs
URS/FS/TS
FAT/SAT
MS Office
Visio

Jobbeschreibung

BioTalent in Switzerland is seeking a Project Engineer / Technical Project Lead to translate requirements into engineering solutions and coordinate multidisciplinary activities across projects. You will review and approve critical documentation and develop P&IDs to ensure project milestones are met.

Role requires GMP experience, hands-on process equipment knowledge, and strong collaboration with vendors and stakeholders to drive successful outcomes in a regulated environment.

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