Regulatory Affairs Program Director

4 weeks ago

Cambridge, Cambridgeshire, United Kingdom ProductLife Group Full time
{"title": "Regulatory Affairs Program Director", "content": "

Regulatory Affairs Program Director

At ProductLife Group, we are seeking a highly skilled Regulatory Affairs Program Director to lead our outsourcing projects and programs for major clients in Europe.

Your key responsibilities will include:

  • Project management of programs, ensuring workload management, resource allocation, performance review, and cost review.
  • Line management of employees onboarded to programs, including training, individual development plans, salary reviews, and promotions.
  • Communication with clients and internal stakeholders to ensure seamless information exchange.
  • Guaranteeing the delivery of high-quality RA services to clients within agreed timelines.

Requirements:

  • 8+ years of experience in European Regulatory Affairs.
  • Knowledge of EU RA regulations for pharmaceuticals, medical devices, and combination products.
  • Experience in line management, resource management, and invoice management.
  • Fluent English and excellent communication skills.
  • Top-notch organizational skills, proven leadership skills, and business acumen.
  • Ability to work proactively and as part of a team.

We offer a dynamic and challenging work environment, with opportunities for growth and development. If you are a motivated and experienced Regulatory Affairs professional, we encourage you to apply for this exciting opportunity.", "company": "ProductLife Group"}

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