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Associate Director Regulatory
Job Location:
Monthly Salary:
Posted:
22 August 2026 (20 days ago)
Posted:
Application Deadline:
19 November 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
A regional lead Regulatory role in a global biotech
European Regulatory Lead- London or Cambridgewith hybrid working
If youre looking for an opportunity to work as part of a global teamand utilise a breadth of European regulatory capability in a region-lead role this could be an excellent opportunity for you with aground-breaking global biotechnology company with a focus on ethical innovation.
Potentially suited to either an experienced in-house practitioner or someone looking for their first role from practice either individual would find substantial support across an experienced team both locally and throughout the business global hubs.
Role
We are an equal opportunities recruiter committed to ensuring an inclusive and supportive recruitment process. We embrace and promote diversity as we understand the importance and value of this both for us and our clients.
European Regulatory Lead- London or Cambridgewith hybrid working
If youre looking for an opportunity to work as part of a global teamand utilise a breadth of European regulatory capability in a region-lead role this could be an excellent opportunity for you with aground-breaking global biotechnology company with a focus on ethical innovation.
Potentially suited to either an experienced in-house practitioner or someone looking for their first role from practice either individual would find substantial support across an experienced team both locally and throughout the business global hubs.
Role
- Focusing primarily on regulatory and quality matters of medical technology products including RUO and clinical offerings
- Advise the business and its teams/functionsglobally (EMEALA) on complexregulatory frameworks
- Working closely with teams across Reg Affairs Med Affairs Marketing Compliance and Commercial among others
- Supporting regional submissions market-access strategies and post-market matters
- Evaluating and providing cross-function guidance on regulating changes and industry adaptations
- UK or dual UK/EU Qualified
- Senior advisory and commercial experience in a regulatory setting ideally in an international setting
- Demonstrable life sciences and medical devices regulatory knowledge/experience
- An essential skill will be providing practical solutions from analytical judgement of regulatory risk and/or change
- Multilingual skills an advantage but not essential
- Pragmatic and commercially focused with excellent interpersonal skills
- 25 days annual leave plus bank holidays
- Pension plan
- Flexible time off
- Bonus scheme
- Private Medical Insurance
- Life Assurance
- On-site gym
We are an equal opportunities recruiter committed to ensuring an inclusive and supportive recruitment process. We embrace and promote diversity as we understand the importance and value of this both for us and our clients.
Required Experience:
Director
About Company
Legal Recruitment Specialists, talk to the experts. Local knowledge, expert guidance. Focusing on the out-of-London market. Solicitor jobs Cambridge, Solic…
