Regulatory Affairs Manager

Reference: LS-10921_1750949201

Regulatory Affairs Manager

I am working with a pharmaceutical/ Medical Device manufacturing site based in Deeside specialising in challenge meals, this is a good opportunity for a experienced Regulatory Affairs Manager to develop their career with an expanding company.

Key responsibilities for the Regulatory Affairs Manager

  • Develop and implement regulatory strategies for FDA and MHRA submissions.
  • Lead the preparation, submission, and lifecycle management of regulatory dossiers.
  • Work closely with the director with FDA and MHRA, coordinating meetings, and inspection readiness.
  • Monitor changes in global regulatory landscapes and assess impact on ongoing and future projects.
  • Provide regulatory guidance during product development, labelling, and promotional review processes.

Requirements for the Regulatory Affairs Manager

  • Bachelor's degree in a scientific discipline or a related subject.
  • Minimum 5 years' experience in regulatory affairs, with demonstrable expertise in both FDA and MHRA regulatory processes.
  • Strong knowledge of global regulatory standards
  • Proven success in authoring and managing regulatory submissions and renewals.
  • Excellent communication, leadership, and project management skills.

Benefits for the Regulatory Affairs Manager

  • 25 holidays per year + Bank Holidays
  • Christmas shutdown.
  • Cycle to work scheme
  • Private healthcare
  • High street discount scheme

To apply for the Regulatory Affairs Manager or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email me at

£55,000.00 - £65,000.00
Per annum
Negotiable

Chester

Permanent

Added 26/06/2025
Reference: LS-10921_1750949201

Regulatory Affairs Manager

Chester
Permanent

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