Regulatory Affairs Project Manager

2 weeks ago


Cambridge, Cambridgeshire, United Kingdom ProductLife Group Full time

ProductLife Group is seeking a Regulatory Affairs Project Manager

We are looking for an experienced professional to lead our Regulatory Affairs outsourcing projects/programs in the UK. The ideal candidate will have a deep understanding of EU RA regulations and be able to coordinate multiple projects simultaneously.

About Us

At ProductLife Group, we pride ourselves on delivering high-quality services to our clients. As a Regulatory Affairs Project Manager, you will be responsible for ensuring the successful delivery of our RA services to clients in Europe.

Your Key Responsibilities

  • Project Management: Ensure the timely and qualitative delivery of RA services to clients in accordance with agreed timelines.
  • Client Communication: Act as a direct point of contact with clients, coordinating communication between internal teams and external stakeholders.
  • Team Management: Line manage employees working on RA programs, providing guidance, support, and development opportunities.
  • Resource Allocation: Manage resources effectively to meet project demands, ensuring efficient workload distribution and allocation.

You Will Have:

  • 8+ years experience in European Regulatory Affairs
  • Knowledge of EU RA regulations for pharmaceuticals (NCEs, Biologicals, and Biotech), Medical Devices, Combination products
  • EDMS, Regulatory Databases (Register) knowledge
  • Line management and resource management experience
  • Fluent English mandatory
  • Excellent communication, organizational, and leadership skills

The Salary for this position is £80,000-£100,000 per year, depending on experience.



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