Facilities & Utilities Engineer

  • Salary: Competitive
  • REF Number: v-181288
  • Consultant: Robert Angrave
  • Contact: 01246 457716
  • Date Published: 07.04.2026
  • Industry: Pharmaceutical
  • Location: Neuchâtel, Switzerland
  • Functional Expertise: Other

Plant Engineer (Facilities & Utilities) – Interim Contract

Location: Switzerland

Duration: Short-term contract

We are currently supporting a leading pharmaceutical manufacturing site with the appointment of an experienced Plant Engineer (Facilities & Utilities) on an interim basis.

This role will provide critical engineering expertise to support site operations, ensuring the reliability, compliance, and continuous improvement of facilities and utility systems in a highly regulated environment.

Key Responsibilities

  • Act as Subject Matter Expert (SME) for Facilities & Utilities systems including HVAC, clean utilities, black utilities (chillers, boilers), buildings, and chemical storage/distribution.
  • Provide technical support for investigations, deviations, and recurring issues.
  • Lead and/or support design, installation, commissioning, and qualification activities.
  • Drive continuous improvement initiatives and system optimizations.
  • Ensure equipment and systems remain fit for purpose, proposing and implementing corrective actions where required.
  • Coordinate modifications, upgrades, and maintenance activities.
  • Ensure compliance with cGxP, Good Engineering Practices (GEP), and relevant industry standards.
  • Support internal and external audits as a technical expert.
  • Contribute to the development and implementation of engineering procedures and standards.
  • Ensure all activities are carried out in line with safety requirements.
Requirements

  • Degree in Mechanical Engineering, Chemical Engineering, Biotechnology, or related discipline.
  • Minimum 5 years’ experience within the pharmaceutical or biotech industry.
  • Strong background in Facilities & Utilities within GMP environments.
  • Experience with installation, commissioning, and validation of pharmaceutical systems.
  • Good understanding of cGxP, regulatory expectations, and industry guidelines.
  • Fluency in French and English (German is an advantage).
  • Strong problem-solving skills and a proactive, hands-on approach.
  • Ability to work effectively in a fast-paced, cross-functional environment.
Additional Information

This is an excellent opportunity for an experienced contractor to join a high-performing site and contribute to critical operations and improvement projects. If you are wanting to apply, please contact CK QLS on +41 444 990 468.

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