Industrial Project Manager – GMP/CQV Expansion

VENS sp. z o.o.; Paris; Sur place; EUR 90 000 - 130 000; Plein temps

Avantages offerts par ce poste

Co-financing of courses and training

Referral programme

Résumé du poste

VENS sp. z o.o. seeks an experienced Project Manager to drive CAPEX capacity expansions and production-line improvements in an industrial facility in Paris. You will oversee CIP, infrastructure, utilities, HVAC, and fire protection upgrades, ensuring strict adherence to budget, schedule, and quality requirements.

The role demands on-site leadership, fluent French and English, and a strong background in GMP/CQV standards within the food or pharmaceutical sectors.

Qualifications

• Fluent French and English (min. B2) for on-site coordination with local teams and contractors.
• 5+ years in industrial construction, including project management and budget control.
• Experience in food or pharmaceutical industries with GMP/CQV knowledge is a strong asset.

Responsabilités

• Lead comprehensive CAPEX projects from specification through commissioning and start-up.
• Supervise upgrades of production lines, CIP, infrastructure, utilities, HVAC and fire protection systems.
• Plan, control and report to ensure budget, schedule and quality targets are met.
• Ensure compliance with construction laws and corporate standards (NFPA, GMP/CQV, HACCP/GHP).
• Coordinate with OHS, maintenance, Controlling and external contractors; report progress to steering bodies.

Connaissances

French language

English proficiency

Negotiation

Formation

Higher engineering degree

Outils

AutoCAD

MS Office

Scheduling tools

Description du poste

VENS sp. z o.o. seeks an experienced Project Manager to drive CAPEX capacity expansions and production-line improvements in an industrial facility in Paris. You will oversee CIP, infrastructure, utilities, HVAC, and fire protection upgrades, ensuring strict adherence to budget, schedule, and quality requirements.

The role demands on-site leadership, fluent French and English, and a strong background in GMP/CQV standards within the food or pharmaceutical sectors.