Regulatory Affairs Manager at Kleboe Jardine Ltd
London, Essex - England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

10 Nov, 26

Salary

55000.0

Posted On

06 Oct, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

About the job


We are supporting an established and innovative medical technology business with the appointment of a Regulatory Intelligence Manager to strengthen its global Regulatory Affairs capability.

This is a strategically important role responsible for identifying, interpreting and communicating emerging regulatory requirements, health authority expectations and industry developments across global markets. The successful candidate will translate regulatory intelligence into clear, practical actions that influence product strategy, lifecycle management, technical documentation, submissions and market access.

The role will suit an experienced regulatory professional who enjoys looking beyond individual submissions and taking a broader view of how changes in regulation may affect products, processes and commercial strategy.

You will act as a central point of expertise for regulatory intelligence, working closely with Regulatory Affairs, Quality, Clinical, Product Development and senior leadership teams across a portfolio incorporating both medical device hardware and software.

  • Key responsibilities will include:Monitoring global regulatory developments, guidance, standards, enforcement trends and health authority expectations.
  • Assessing the potential impact of regulatory changes on products, technical files, processes, clinical activity and market access.
  • Translating complex regulatory developments into clear recommendations, implementation plans and risk-mitigation actions.
  • Developing and improving structured regulatory intelligence and surveillance processes.
  • Providing strategic regulatory advice to product and project teams throughout the product lifecycle.
  • Monitoring competitor activity and wider medical device industry developments.
  • Supporting regulatory strategy for new and existing products across international markets.
  • Working with authorities including the MHRA, EMA and FDA where appropriate.
  • Producing dashboards, metrics and senior-management reports covering emerging risks, opportunities and regulatory trends.
  • Establishing and monitoring Regulatory Intelligence KPIs to demonstrate the impact and effectiveness of the function.


Responsibilities
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