Project Manager / Deputy GMP Engineering Manager

JR France; Rennes; Sur place; EUR 80 000 - 120 000; Plein temps

Résumé du poste

A leading company is looking for a Project Manager / Deputy GMP Engineering Manager for a major site expansion project in France. This role involves overseeing technical teams, ensuring compliance with pharmaceutical standards, and managing project budgets and timelines. Ideal candidates should have extensive experience in the pharmaceutical engineering field and valid GMP training.

Qualifications

• 15+ years of experience in large pharmaceutical engineering projects (>€100M).
• Expertise in aseptic processing and clean utilities.

Responsabilités

• Lead and coordinate technical teams.
• Ensure compliance with GMP and pharmaceutical standards.
• Draft and manage contracts with suppliers.

Connaissances

Coordination skills

Stakeholder management

Formation

GMP training certificate

Description du poste

Social network you want to login/join with:

Project Manager / Deputy GMP Engineering Manager, centre

col-narrow-left

Client:

Blackfield Associates

Location:

centre, France

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

240263172502165913632760

Job Views:

2

Posted:

08.06.2025

Expiry Date:

23.07.2025

col-wide

Job Description:

Location: France

Type: Contract, initially 4 months (chance of extension)

Project Overview

The role supports a major site expansion project, including a QC lab extension, clean/industrial utilities building, and effluent neutralization plant.

Main Responsibilities

• Lead and coordinate technical teams (HVAC, utilities, process, electrical).
• Review and validate technical studies and specifications.
• Draft and manage contracts with suppliers and subcontractors.
• Track project progress, budget, risks, and report regularly.
• Identify and resolve technical and organizational issues.
• Ensure compliance with GMP and pharmaceutical standards.
• Act as a link between engineering firms, developer, and internal teams.
• Project plan, specifications, contracts
• Meeting minutes, progress reports, KPIs
• Planning, budget, cash flow, risk and change documents
• Roles and responsibilities matrix

Requirements

• 15+ years of experience in large pharmaceutical engineering projects (>€100M)
• Expertise in aseptic processing, clean utilities, GMP batch interface
• Strong coordination and stakeholder management skills
• Valid GMP training certificate required before mission starts