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Senior Manager Global Regulatory Affairs

JR United Kingdom

Bristol
Presencial
GBP 70.000 - 90.000
Hace 30+ días
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Senior Manager Global Regulatory Affairs
JR United Kingdom
Bristol
Presencial
GBP 70.000 - 90.000
Jornada completa
Hace 30+ días

Descripción de la vacante

A specialized recruitment firm seeks a Senior Manager Global Regulatory Affairs in Bristol. The role involves managing regulatory requirements and interactions with authorities like the FDA and EMA, while leading teams and driving strategic initiatives. The ideal candidate will have deep knowledge in Regulatory Affairs, particularly with ATMP and Rare Disease products, and possess strong leadership and communication skills.

Formación

  • In-depth Regulatory Affairs experience across the EU and US from early development through to post-approval.
  • Understanding of HTA requirements and expedited programs.
  • Track record in managing high-level regulatory authority interactions.

Responsabilidades

  • Act as a subject matter expert on global regulatory requirements.
  • Provide strategic and operational regulatory leadership.
  • Lead regulatory interactions with authorities such as the FDA and EMA.
  • Manage external regulatory service providers.
  • Drive internal training and ensure regulatory awareness.

Conocimientos

Regulatory Affairs expertise
Leadership skills
Negotiation skills
Problem-solving abilities
Communication skills

Educación

BSc or equivalent in life science or legal discipline
Descripción del empleo

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Senior Manager Global Regulatory Affairs, bristol

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Client:

Mantell Associates

Location:

bristol, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

1

Posted:

22.08.2025

Expiry Date:

06.10.2025

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Job Description:

Mantell Associates is currently partnered with an exciting Biomedical Research organisation, who are looking to bring in a Global Regulatory Affairs Senior Manager to take the company to new heights as they continue to grow.

Senior Manager Global Regulatory Affairs - Responsibilities:

  • Act as a subject matter expert on global regulatory requirements, including for ATMPs, ensuring company-wide compliance and integrating relevant regulatory intelligence
  • Provide strategic and operational regulatory leadership across project teams, including resource allocation, risk identification, and mitigation planning
  • Lead regulatory interactions with authorities such as the FDA, EMA, and national agencies, while overseeing the preparation and submission of high-quality regulatory documents (e.g., IMPD/CTA/IND, MAA/BLA, orphan drug and breakthrough designation applications)
  • Manage external regulatory service providers to align with business objectives and support the development and maintenance of an effective regulatory affairs function
  • Drive internal training, ensure regulatory awareness, and contribute to company policies and governance as the organisation evolves

Senior Manager Global Regulatory Affairs - Requirements:

  • BSc or equivalent in a life science or legal discipline, with in-depth Regulatory Affairs experience across the EU and US from early development through to post-approval
  • Proven experience with ATMP and/or Rare Disease products, with understanding of HTA requirements, accelerated pathways, and conditional approvals within FDA and EMA frameworks
  • Demonstrated success in regulatory strategy development, multi-project leadership, and managing high-level regulatory authority interactions
  • Strong leadership, communication, negotiation, and organisational skills, with a track record of creative problem-solving and effective issue management in regulatory contexts
  • Familiarity with expedited programs such as breakthrough designation and a collaborative approach to cross-functional engagement

Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact us at 44 (0)20 3854 7700.

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