Commissioning Project Manager - Equipment/Process (M/F)

Meent Life SciencesSeine-MaritimeEURESpublished 09/22/2026
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Machine translation — original language: French.Show original

Joining Meent means?

Joining an engineering company expert in Life Science, created in 2023, which values the talent and energy of its employees to carry out innovative and ambitious projects.

At Meent Life Science, we build an adventure with our employees based on:

  • Mutual aid and team spirit
  • Benevolence and stability
  • Fulfillment and professional progression

We believe that a fulfilled employee is a high-performing employee. That is why we offer a stimulating environment, training opportunities, and long-term support in your career.

The position:

  • Lead activities related to the integration of new process equipment in a pharmaceutical industrial environment.
  • Ensure the interface with the project management and contracted companies, from detailed studies to commissioning.
  • Collect, structure, and transmit the data necessary for technical studies.
  • Control and monitor the detailed study deliverables produced by partner companies.
  • Coordinate process equipment packages, particularly on perimeters related to propellant gases and vapor recovery units.
  • Perform technical installation audits on-site.
  • Verify the compliance of installations with current pharmaceutical standards, regulations, and requirements.
  • Contribute to commissioning and equipment qualification activities, in connection with the dedicated C&Q team.
  • Proactively monitor the execution schedule and anticipate any deviations.
  • Ensure the monitoring of company costs and ensure compliance with budgetary commitments.
  • Guarantee the adequacy between costs, deadlines, quality of deliverables, and requirements defined in the tender.
  • Collaborate with internal teams, external partners, and project stakeholders in a demanding technical context.

Profile sought:

  • You have at least 10 years of experience in project management for equipment, process, or new works in industry.
  • You have worked in a pharmaceutical environment.
  • You are familiar with GMP / GxP requirements and the compliance issues associated with industrial installations.
  • You have already worked on projects involving an EPCM contractor or external project management.
  • You master the monitoring of studies, construction sites, commissioning, and qualification of process equipment.
  • Experience in an ATEX zone is required or strongly appreciated.
  • Experience on a Seveso site would be a plus.
  • You speak English fluently in an international project context.