Regulatory Affairs Leader

1 month ago


Greater Manchester, United Kingdom Radar Recruitment Full time

We are supporting a Pharmaceutical business as they seek to bring on board a new Head of Regulatory Affairs to join them at an exciting phase of growth.

About the business: This organisation is well established, has a diverse customer base, and is well geared for growth in the coming years. The business supplies a range of pharmaceutical products into multiple segments of the healthcare sector and has a strong reputation as one of the leaders within this field. They have a diverse and inclusive culture, and you will get the opportunity to not only lead and work alongside a talented regulatory affairs team but also work cross-functionally with the wider business.

About the role: The Head of Regulatory Affairs will lead the Regulatory Affairs team and is responsible for maintaining/reviewing existing licences as well as implementing new licences. You will have overall responsibility for contributing towards optimum levels of regulatory compliance and supporting the wider business with achieving its commercial goals. Some of the key responsibilities for the Head of Regulatory Affairs role will involve:

  • Leading the Regulatory Affairs team, including all line management responsibilities.
  • Ensuring that all licences comply with the regulations set by the Regulatory Authority.
  • Ensuring timely submission of all new licence applications and licence variations by the Regulatory Affairs team.
  • Ensuring all members of the Regulatory Affairs team are adequately trained to perform the tasks required.
  • Training, mentoring, and developing members of the Regulatory Affairs team.
  • Keeping all licence portfolios continuously up to date with the latest requirements from the regulatory bodies and free from errors.

The successful candidate for the Head of Regulatory Affairs role will have the following background:

  • Extensive experience working in a leadership/management role within a Regulatory Affairs team in the Pharmaceutical sector.
  • Strong knowledge and understanding of regulatory processes in GMP environments.


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