This site uses cookies. By continuing to use this site you consent to our use of cookies. Close
MUJO Jobs
Sign In Register Advertise With Us
menu
  • clear
  • Home
  • About Us
  • Find a Job
  • Career Advice
  • Job Alerts
  • Contact Us
  • Sign In Register Advertise With Us
    • Login
    • Register
  • Home
  • Jobs
  • Job Alerts
  • News & Advice
Hiring?
More options

Job Description

« Back to results
Company Name : Cure Talent Ltd
3123527113
£65000.00 - £80000.00 Annual | Bonus, Pension, Private Healthcare
Permanent
Cheshire East, United Kingdom
Not stated on job
Senior manager
17-06-2026
Apply Now

Email has sent successfully.

Please check your email .

Regulatory Affairs Manager

Apply Now

Cure Talent are delighted to be partnered with a global CDMO specialising in complex drug-device combination products, as they continue to expand their Regulatory Affairs capability following a period of significant growth.

As part of an ongoing reorganisation, the business is growing its regulatory team and appointing Regulatory Manager to lead project delivery across a diverse portfolio of combination products, with a strong focus on inhalation and respiratory devices. This is a client-facing, hands-on leadership role where you will be responsible for driving regulatory strategy and delivery across multiple projects, acting as the regulatory subject matter expert and primary point of contact for customers and regulatory agencies.

As the Regulatory Manager, you will lead the regulatory aspects of development programmes, contributing to project planning, advising on regulatory pathways and ensuring high-quality submission content, with particular focus on Module 3 authoring. You will work closely with internal teams and external clients, providing clear, confident regulatory guidance and challenging where required to ensure compliant and efficient routes to market.

This role combines leadership with delivery. While you will have responsibility for mentoring and developing team members, this is not a role for someone who wants to step away from the detail. You will remain hands-on, owning projects and contributing directly to regulatory documentation and submissions.

To be successful as the new Regulatory Manager, you will bring proven experience authoring Module 3 documentation for drug-device combination products or inhalation / respiratory drug products. You will be confident operating in a client-facing environment, able to define and defend regulatory strategy, and comfortable taking ownership of complex programmes as the regulatory lead.

Key Responsibilities

  • Lead regulatory strategy and delivery for drug-device combination development programmes.
  • Author and review regulatory documentation, with direct ownership of Module 3 content.
  • Act as the primary regulatory contact for clients and external regulatory agencies.
  • Provide regulatory input into project planning, timelines and resource requirements.
  • Review and approve regulatory documentation prepared by Specialists and Associates.
  • Support and mentor team members, driving performance and development.
  • Contribute to regulatory intelligence and advise on evolving regulatory requirements.
  • Represent the regulatory function in client meetings and internal governance forums.

Experience and Skills Required

  • Proven experience authoring Module 3 documentation as part of regulatory submissions.
  • Experience within drug-device combination products or inhalation / respiratory delivery systems.
  • Strong understanding of global regulatory requirements for combination products.
  • Experience operating in a client-facing or consultancy/CDMO environment is advantageous.
  • Ability to manage multiple projects and influence stakeholders at all levels.
  • Strong communication skills and confidence in presenting and challenging regulatory strategy.

This is a high-impact role within a growing organisation where Regulatory plays a central role in client delivery and product development. It will suit someone who is comfortable in the detail, confident in front of clients and capable of leading regulatory workstreams end-to-end.

Apply Now
close

Email this job

Processing, please wait
To include multiple email addresses, please separate them with commas (,).
close

Match CV to job and register - Regulatory Affairs Manager


Apply to this job
  • Regulatory Affairs Manager OTC Reading £60.00 - £70.00 Hour
  • Quality Assurance & Regulatory Affairs Specialist - MedTech Cambridge £45000.00 - £49000.00 Annual
  • Care Compliance Administrator Haddenham £32000.00 - £35000.00 Annual
  • Senior Housing Regulatory Assurance Officer Oxford £30.00 - £30.00 Hour
  • Service Manager (Registered Manager) £35000.00 - £35000.00 Annual
  • Service Manager (Registered Manager) Midhurst £35000.00 - £35000.00 Annual
  • Registered Manager United Kingdom £40000.00 - £40000.00 Annual
  • Home Manager Kettering £30000.00 - £30000.00 Annual
  • Registered Manager Birmingham £60000.00 - £60000.00 Annual
  • Registered Manager Colchester £55000.00 - £55000.00 Annual
close

Apply this job

Click OK to Apply Manage your account
close

Saved Successfully!!!.


close

You're about to be taken to the employer's website to complete your application.
Please either log in, or enter your name and email address before we re-direct you

We are now directing your application to one of our trusted partners to complete the application.

close

Registration

Registered Successfully!!!. We have sent you a confirmation email to your email address.
Apply
close

Verify Your Account

We've sent a verification code to

Time remaining:
Verifying...
Code expired. Please request a new one.
Verify & Register
Didn’t receive the code? 
close You must sign in / sign up to save or apply to job opportunities.
  • Sign In
  • Sign Up

Create an Account

Your Preferences

(word/pdf/rtf/textfiles)

Contact Preferences

In addition to providing our recruitment services to you, we may want to occasionally contact you to let you know about our recruitment services, industry insights, employment news and competitions. 

You will be able to update your preferences or delete your account/information at any time by logging into your account or making a request via email or phone.



Already registered?

Sign in with your account

Use your social media account to register (Don't worry we won't post anything)

LinkedIn
By connecting your social account, you are agreeing to our Terms & Conditions and Privacy Policy.

Login to your account


Forget your Password ?

click here to reset your password

- or sign in using -
Facebook
LinkedIn
By connecting your social account, you are agreeing to our Terms & Conditions and Privacy Policy
Not got an account? Please register here

mujo.com is brought to you by International Medical Information. For more details. visit http://www.medicalimi.com

Disclaimer: All information on this site has been collated by healthcare professionals from around the globe. Where every possible step has been taken to ensure its accu-racy, MedicalUpdateOnline cannot accept responsibility for the authenticity of the content matter.

Copyright: The copyright of the material on this site rests with the author unless otherwise indicated. It is a breach of copyright to use any material from this site without prior written consent.

Jobs
Jobs
  • Upload CV
  • Find a job
  • Job alerts
  • Career advice
  • Recruiter A-Z
Candidate
More Info
  • Sign in
  • Register
Recruiter
  • Advertise with us
  • Sign in
  • Register
More Info
Community
  • About us
  • Terms and Conditions
  • Privacy policy

Subscribe for job alerts

If you're a healthcare professional, you can sign up for our job alerts to receive high-quality opportunities in medicine, pharmaceuticals, and healthcare. Get the latest jobs and updates across a broad range of specialties delivered straight to your inbox.

Copyright © ICR (UK) Limited t/a International Medical Information (IMI). Registered in the UK Company no. 05894351

Powered by Talenetic Job Board Software

arrow_upward