Fmaservices

FMA Services is looking for a Senior Piping & Mechanical Supervisor for projects within the pharmaceutical industry. In this role, you will be responsible for the coordination and follow-up of clean piping and clean utilities installations. You will ensure correct execution according to the highest quality and hygiene standards and manage teams on site. Thanks to your experience in pharma projects and knowledge of hygienic design, you are a key figure in the successful realization of these installations.

What are you going to do?

• Coordinating and monitoring clean piping and clean utilities (WFI, PW, clean steam, CIP/SIP) installations.
• Managing and guiding teams (fitters, welders, and subcontractors).
• Overseeing orbital welding (GTAW) and compliance with welding procedures (WPS/PQR).
  Checking isometrics, P&IDs, and 3D models.
  Monitoring material traceability (MTRs, heat numbers) and QA documentation.
• Monitoring hygienic design criteria such as surface finish, dead legs, and drainability.
• Coordinating passivation, flushing, cleaning, and sterilization processes (SIP).
• Supervising pressure tests, boroscopy inspections, and other quality controls.
• Monitoring mechanical completion and handover to commissioning and validation.
  Ensuring compliance with GMP, GDP, and pharmaceutical quality standards. Participate in FAT/SAT and provide support for IQ/OQ processes.
• Serve as the point of contact for the client and project team on the construction site.

What do we expect from you?

• At least 7 years of experience within pharmaceutical projects (clean piping / hygienic design).
• Thorough knowledge of ASME BPE, orbital welding, and hygienic piping systems.
• Experience with clean utilities such as WFI, PW, clean steam, and CIP/SIP.
• Knowledge of QA/QC processes, traceability, and GMP documentation.
• Experience with inspections such as boroscopy, weld logs, and test packs.
• Strong in reading and interpreting P&IDs, ISOs, and technical plans.
• Leadership skills and a structured approach.
• Safety and quality conscious (VCA VOL and GMP awareness are a plus).
• You can work both independently and collaborate efficiently with various teams.

What do we offer you?

• A responsible position within high-tech pharmaceutical projects.
• Working in a GMP environment where quality and precision are paramount.
• Opportunities to further develop yourself within a specialized sector.
• Competitive remuneration and long-term partnerships.
• Support from an experienced and technically strong team.

Region

Belgium (pharmaceutical clusters)

Interested?

Send us your CV today via the application form or contact us. We would be happy to discuss with you whether you are the right match for this position.

#J-18808-Ljbffr