Engineering Project Manager

Quanta Consultancy Services Ltd; Paris; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading global pharmaceutical company is seeking an Engineering Project Manager to oversee coordination and specification development for large-scale engineering projects in the pharmaceutical sector. Ideal candidates should have proven project management experience, knowledge of pharmaceutical engineering, and proficiency in GMP. Fluency in English is essential for collaboration with international teams. This is a permanent contract located in the South of Paris.

Qualifications

• Proven experience in managing large-scale engineering projects in the pharmaceutical sector.
• Excellent knowledge of pharmaceutical engineering requirements.
• Proficiency in Good Manufacturing Practices (GMP) and SRV processes.

Responsabilités

• Organise and lead coordination meetings between various technical teams.
• Ensure implementation and follow-up of actions from meetings.
• Coordinate development of specifications and technical specifications.
• Supervise and approve design studies.
• Oversee contracts with suppliers and subcontractors.

Connaissances

Project management

Stakeholder coordination

Good Manufacturing Practices (GMP)

Fluency in English

Description du poste

Engineering Project Manager - South of Paris - Permanent Contract

Our client, a global pharmaceutical company, is looking for an Engineering Project Manager to join their team. The company has grown to become a world leader in the development, manufacture, and marketing of innovative pharmaceutical products to alleviate some of the world’s biggest health problems.

What you'll do

• Organise and lead coordination meetings between the various technical teams (HVAC, clean utilities and industrial, process, electricity, etc.) to ensure alignment of actions and objectives.
• Ensure the implementation and follow-up of actions resulting from these meetings.
• Coordinate the development of specifications and technical specifications, ensuring they meet the specific needs of the ancillary project.
• Supervise and approve design studies.
• Oversee the drafting and signing of contracts with suppliers and subcontractors, ensuring compliance with legal and regulatory requirements.

What you'll need

• Proven experience in managing large-scale engineering projects in the pharmaceutical sector, ideally on aseptic production or clean utility projects.
• Excellent knowledge of pharmaceutical engineering requirements.
• Proven ability to coordinate various stakeholders and facilitate interactions between multidisciplinary teams.
• Proficiency in Good Manufacturing Practices (GMP) and SRV processes as part of qualification/validation activities in a pharmaceutical environment.
• Fluency in English is essential for communicating with international teams and suppliers.

If you would like to apply or find out more, get in touch now!