Senior Manager, Regulatory Affairs
Hybrid · Maidenhead, England, United Kingdom
Job Summary
Lead and oversee UK Regulatory Affairs with line-management responsibility for a small team; provide regulatory strategy and tactical execution across product lifecycle, including submissions to MHRA, pediatric plans, variations, and marketing authorisations; build and maintain relationships with MHRA, ABPI, and cross-functional partners; guide the team on regulatory landscape, liaise with area/affiliate members, support product launches, acquisitions, and divestitures, and ensure compliance with UK regulations and AbbVie policies.
Required Qualifications
- Life Sciences Degree in relevant subject area
- Experience as a line manager
- Regulatory affairs experience in the pharmaceutical industry (UK)
- Strong knowledge of MHRA submissions and UK regulatory requirements
- Excellent written, verbal and interpersonal skills in English
- Ability to multitask and manage multiple projects and deadlines
- Strong diplomacy and stakeholder management skills
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