Commissioning Manager

Alsinova

Limburg

Sur place

EUR 100 000 - 160 000

Plein temps

14 jours+
Générateur de candidature

Une candidature sur mesure pour ce poste — un CV et une lettre de motivation personnalisés qui correspondent à l’offre.

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Résumé du poste

Alsinova seeks an experienced Commissioning Lead to drive the commissioning and handover of a GMP and nuclear facility. You will manage strategy, sequencing, testing and gatekeeping across building, utilities, process and automation systems, coordinating vendors and regulatory stakeholders including FANC.

You will ensure documentation completeness, transfer to Operations/CMMS and safe execution of activities such as LOTO. Fluency in English is required, with French/Dutch a plus.

Qualifications

  • 10+ years of experience in commissioning within pharmaceutical, nuclear or other highly regulated industries.
  • Strong experience with FAT/SAT, IQ/OQ/PQ and GMP environments.
  • Broad understanding of HVAC, utilities, process, electrical and control systems.
  • Proven ability to coordinate multiple stakeholders and manage complex project interfaces.
  • Fluent in English. French and/or Dutch is a plus.

Responsabilités

  • Manage the overall commissioning strategy, sequencing, testing and handover plan.
  • Coordinate integrated commissioning activities across building, utilities, process and automation systems.
  • Lead cross-functional testing and ensure readiness for operational handover.
  • Maintain the commissioning register and enforce acceptance and testing gates.
  • Coordinate vendors, contractors, operations teams and regulatory stakeholders (including FANC).
  • Ensure commissioning documentation is complete, compliant and transferable to Operations and CMMS.
  • Drive safe execution of commissioning activities, including LOTO management.

Connaissances

Commissioning leadership
IQ/OQ/PQ validation
GMP environments
HVAC understanding
Stakeholder coordination
Regulatory liaison
English fluent

Description du poste

Join a pioneering radiopharmaceutical manufacturing project and lead the commissioning and operational handover of a highly regulated GMP and nuclear facility.

Key Responsibilities
  • Manage the overall commissioning strategy, sequencing, testing and handover plan.
  • Coordinate integrated commissioning activities across building, utilities, process and automation systems.
  • Lead cross-functional testing and ensure readiness for operational handover.
  • Maintain the commissioning register and enforce acceptance and testing gates.
  • Coordinate vendors, contractors, operations teams and regulatory stakeholders (including FANC).
  • Ensure commissioning documentation is complete, compliant and transferable to Operations and CMMS.
  • Drive safe execution of commissioning activities, including LOTO management.
Profile
  • 10+ years of experience in commissioning within pharmaceutical, nuclear or other highly regulated industries.
  • Strong experience with FAT/SAT, IQ/OQ/PQ and GMP environments.
  • Broad understanding of HVAC, utilities, process, electrical and control systems.
  • Proven ability to coordinate multiple stakeholders and manage complex project interfaces.
  • Fluent in English. French and/or Dutch is a plus.
Personal Qualities

We are looking for someone who is:

Structured, pragmatic and results-driven.

Comfortable enforcing project gates and escalating critical issues.

A natural integrator who thrives in multidisciplinary environments.

Motivated by contributing to the scale-up of life‑saving radiopharmaceutical production.

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