Speculative - Maintenance Engineer (M / F)

Barrington James; Roubaix; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading life sciences recruitment firm in North of France is seeking a Maintenance Engineer to contribute to innovative projects in the pharmaceutical and biotechnology fields. The ideal candidate will have a Bac+5 in engineering, fluency in French, and experience within a CDMO environment. This role involves maintenance of production equipment, participation in project phases, and ensuring regulatory compliance.

Prestations

Participate in innovative projects

Dynamic international environment

Qualifications

• Prior experience in a CDMO or pharmaceutical/biotechnology environment is highly preferred.
• Experience in greenfield projects or commissioning industrial facilities is a major asset.
• Good knowledge of GMP regulations and pharmaceutical industry standards.

Responsabilités

• Provide preventive and corrective maintenance of production equipment and utilities.
• Participate in design and installation phases of equipment on greenfield projects.
• Ensure compliance with regulatory standards and facility performance.
• Contribute to continuous improvement of processes.

Connaissances

Analytical mind

Rigor

Teamwork

Fluency in French

Technical English

Formation

Bac+5 in process engineering, mechanical engineering, pharmacy or chemistry

Description du poste

Job title: Maintenance Engineer (M / F). Location: North of France. Type of application: Spontaneous / Future project.

Overview

As part of potential future projects within a CDMO (Contract Development and Manufacturing Organization) environment, we are looking to anticipate a need for a Maintenance Engineer. The position will mainly concern greenfield and / or site expansion projects, in a highly regulated context (pharmaceutical, chemical or biotechnology industry).

Main missions

• Provide preventive and corrective maintenance of production equipment and utilities (HVAC, air treatment systems, process equipment, etc.).
• Actively participate in the design, installation and qualification phases of equipment on greenfield projects.
• Collaborate with production, quality and engineering teams to ensure regulatory compliance (GMP) and facility performance.
• Contribute to the continuous improvement of processes and the optimization of maintenance interventions.
• Ensure documentary monitoring and traceability of interventions in compliance with quality and safety standards.

Profile sought

• Bac+5 training in process engineering, mechanical engineering, pharmacy, chemistry or engineering.
• Prior experience in a CDMO or pharmaceutical / biotechnology environment highly preferred.
• Previous experience in greenfield projects or commissioning industrial facilities is a major asset.
• Good knowledge of GMP regulations and pharmaceutical industry standards.
• Analytical mind, rigor and ability to work in a team in a demanding environment.
• Fluency in French and good knowledge of technical English.

Why join our future projects?

• Participate in innovative and strategic projects in the pharmaceutical / biotechnology field.
• Contribute to the creation and optimization of modern industrial sites.
• Develop your skills in a dynamic and international environment.