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Project Manager / Deputy engineer manager

  1. France
Paris
  1. Contract
Competitive
  1. Compliance / Quality Assurance
37276
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Project Manager / Deputy engineer manager - France, Paris - 6 Month Contract

Our client, a global pharmaceutical company, are looking for a Project 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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