Regulatory Affairs Program Director

2 months ago

Cambridge, Cambridgeshire, United Kingdom ProductLife Group Full time
Regulatory Affairs Program Director Opportunity

We are seeking a highly experienced Regulatory Affairs Program Director to join our team at ProductLife Group. As a key member of our Regulatory Affairs department, you will be responsible for managing outsourcing projects and programs for major clients in the pharmaceutical industry.

About the Role

As a Regulatory Affairs Program Director, you will act as a direct point of contact with clients and coordinate several outsourcing projects for their Regulatory Affairs activities in Europe. Your main tasks will include:

  • Project management of programs, including workload management, resource allocation, performance review, and cost management
  • Line management of employees onboarded to programs, including training, development planning, and performance evaluation
  • Communication with clients and internal stakeholders to ensure seamless information exchange
  • Guaranteeing the delivery of high-quality Regulatory Affairs services to clients within agreed timelines
Requirements

To be successful in this role, you will need:

  • 8+ years of experience in European Regulatory Affairs, with knowledge of EU RA regulations for pharmaceuticals, medical devices, and combination products
  • Experience in line management, resource management, and invoice management
  • Fluent English language skills and excellent communication skills
  • Top-notch organizational skills, proven leadership skills, and business acumen
  • Ability to work proactively and independently, with a strong sense of personal responsibility
What We Offer

We offer a dynamic and challenging work environment, with opportunities for professional growth and development. If you are a motivated and experienced Regulatory Affairs professional looking for a new challenge, we encourage you to apply for this exciting opportunity.

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