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Regulatory Specialist

Randstad Delivery (GBS)·Dundee (Scotland)On-site12 months
£45 000 / year
Vox Summary
  • Role Overview: Manage regulatory activities as Responsible Person for UK and Swiss markets, overseeing vigilance, regulatory intelligence, change assessments, and interfacing with authorities.
  • Key Requirements: Experience in compliance or regulatory affairs; expertise in regulatory compliance, vigilance, technical documentation; ability to interact with MHRA and Swissmedic.
  • Conditions & Benefits: Full-time, office-based role in Dundee; 12-month contract with potential extension; salary of £45,000 per annum.
  • Skills & Qualities: Strong communication skills, collaborative mindset, self-motivated, capable of briefing executive leadership, with a background in managing complex regulatory interactions.
Apply on sourceYou are leaving VoxJobs for reed.co.uk — the application is handled directly by the company. reed.co.uk

Job description

Are you an experienced professional in regulatory affairs looking for a pivotal role to influence compliance strategies for international markets? Do you possess a strong background in regulatory frameworks and an aptitude for managing complex interactions with health authorities? If you are a collaborative professional ready to take ownership of the UK and Swiss Responsible Person functions, this role offers an opportunity to make a significant impact. Job Title - Regulatory Specialist - UK & Swiss Job Location - Dundee (Full-time, office-based) Job Type - 12 months (potential for extension) Pay rate - £45,000 per annum Job Summary The incumbent will manage regulatory activities as the UK and Swiss Responsible Person for all sites outside Dundee/CMI. Responsibilities include overseeing vigilance, regulatory intelligence, change assessments, and direct interfacing with the MHRA and Swissmedic. You will lead product inclusion activities for UK and Swiss markets, ensuring all products meet stringent regulatory compliance standards. Additionally, you will act as the site lead for assessing changes in regulatory requirements and quality standards, implementing impact assessments, and managing technical documentation on behalf of legal manufacturers. Qualification/education Experience Professional background in compliance or regulatory affairs. Candidates with strong regulatory experience may be trained specifically for the UK and Swiss market requirements. Skills • Expertise in regulatory compliance, vigilance, and technical documentation management. • Proven ability to interface professionally with regulatory bodies such as the MHRA and Swissmedic. • Strong communication skills, capable of briefing executive-level leadership. • Self-motivated with a commitment to continuous professional development. • Strong collaborative mindset to work effectively within a multidisciplinary team. How To Apply Interested candidates should apply through Randstad's website, providing a detailed CV and cover letter outlining their qualifications and experience. Randstad Business Support is acting as an Employment Business in relation to this vacancy.

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Original source
reed.co.uk
Posted
Jul 13, 2026 · true date
Last verified
7 hours ago
Quality score
65/100
Salary stated30
Company identified0
applyUrl0
postedAt15
Complete description20

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