Project Manager / Deputy engineer manager

Quanta Consultancy Services Ltd; Paris; Sur place; EUR 57 000 - 82 000; Plein temps

Résumé du poste

A leading pharmaceutical consultancy in Paris is seeking a Project Manager to oversee large-scale engineering projects in the pharmaceutical sector. The role involves coordinating between various technical teams, ensuring compliance with industry standards, and managing risks and contracts. Candidates should have extensive experience in pharmaceutical engineering and mastery of GMP processes. This is a 6-month contract position.

Qualifications

• Extensive experience in managing large-scale engineering projects.
• Knowledge of Good Manufacturing Practices (GMP) in pharmaceuticals.
• Ability to facilitate coordination between technical teams.

Responsabilités

• Organise coordination meetings across technical teams.
• Oversee contracts with suppliers and subcontractors.
• Establish performance indicators for project monitoring.

Connaissances

Project management

Risk management

Excellent communication

Regulatory compliance

Description du poste

Project Manager / Deputy engineer manager - France, Paris - 6 Month Contract

Our client, a global pharmaceutical company, are looking for aProject Manager / Deputy engineer 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.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:

• Organise and facilitate coordination meetings between the different technical teams (HVAC, utilities, industrial, process, electricity, etc.) to ensure alignment of actions and objectives.
• Ensure the implementation and monitoring of actions resulting from these meetings.
• Oversee the drafting and execution of contracts with suppliers and subcontractors, ensuring compliance with legal and regulatory requirements.
• Establish performance indicators for monitoring the progress of the ancillary project and the allocated budgets.
• Identify, analyse, and manage the risks of the main project and the ancillary project, including claims management.
• Act as a facilitator between the various engineering companies, the project promoter, and the client teams to ensure smooth and effective communication.
• Ensure that the engineering practices applied meet the regulatory standards in the pharmaceutical industry, and that all steps comply with Good Manufacturing Practice (GMP) requirements.

Desirable Experience:

• Extensive/proven experience in managing large-scale engineering projects in the pharmaceutical sector.
• Excellent knowledge of pharmaceutical engineering requirements, particularly regarding aseptic filling processes and washing and sterilisation, clean/industrial utilities, clean rooms, and managing interfaces between GMP batches.
• Knowledge of Best Practices: Mastery of Good Manufacturing Practices (GMP) and SRV processes within qualification/validation activities in a pharmaceutical environment.

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