Regulatory Affairs Manager

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We are hiring a Regulatory Affairs Manager to support regulatory activities across a diverse pharmaceutical portfolio, including both marketed and pre-approval supply pathways. This role suits experienced regulatory professionals or individuals ready to step up into broader responsibility. The RA Manager will be managing 2 direct reports.


Key responsibilities

  1. Lead regulatory activities across assigned products and regions, ensuring compliance with applicable legislation and Good Regulatory Practice.
  2. Provide regulatory guidance to cross-functional teams, including support for special access, pre-approval, or non-standard supply scenarios where required.
  3. Support regulatory capability and process development, contributing to continuous improvement and mentoring within the regulatory function.


About you

  • Degree in Life Sciences or a related discipline
  • Experience in Regulatory Affairs within the pharmaceutical industry
  • Strong understanding of regulatory frameworks, preferably in multiple regions
  • Comfortable working independently and collaboratively
  • Previous people management experience is welcome but not essential

”, “datePosted”: “2026-05-17”, “hiringOrganization”: { “@type”: “Organization”, “name”: “GxPeople Global”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__434953912__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861&geoID=9” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “South East” } } }
Company: GxPeople Global
Apply for the Regulatory Affairs Manager
Location: South East
Job Description:

We are hiring a Regulatory Affairs Manager to support regulatory activities across a diverse pharmaceutical portfolio, including both marketed and pre-approval supply pathways. This role suits experienced regulatory professionals or individuals ready to step up into broader responsibility. The RA Manager will be managing 2 direct reports.

Key responsibilities

  1. Lead regulatory activities across assigned products and regions, ensuring compliance with applicable legislation and Good Regulatory Practice.
  2. Provide regulatory guidance to cross-functional teams, including support for special access, pre-approval, or non-standard supply scenarios where required.
  3. Support regulatory capability and process development, contributing to continuous improvement and mentoring within the regulatory function.

About you

  • Degree in Life Sciences or a related discipline
  • Experience in Regulatory Affairs within the pharmaceutical industry
  • Strong understanding of regulatory frameworks, preferably in multiple regions
  • Comfortable working independently and collaboratively
  • Previous people management experience is welcome but not essential

Posted: May 17th, 2026