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Regulatory Affairs Specialist

2 months ago

Reading, Reading, United Kingdom Actalent Full time
Regulatory Affairs Manager Opportunity

We are seeking a highly skilled Regulatory Affairs Manager to join our team in the UK and Ireland. As a key member of our organization, you will provide expert regulatory guidance and manage all regulatory activities across the region.

About the Role:

  • Provide regulatory expertise to our UK organization.
  • Manage regulatory activities for the UK and Ireland.
  • Serve as the Local Person for Pharmacovigilance (LPPV) and the National Pharmacovigilance Contact Person.
  • Ensure compliance with UK regulatory processes and national drug legislation.

Requirements:

  • Minimum of 6 years of experience in regulatory affairs within the pharmaceutical industry.
  • Expert knowledge of UK regulatory processes and national drug legislation.
  • Strong communication and organizational skills.
  • Ability to work in a fast-paced environment and manage multiple priorities.

What We Offer:

  • A dynamic and innovation-driven work environment.
  • Opportunities for professional growth and development.
  • A competitive salary and benefits package.