Regulatory Affairs Contract Jobs in Cardiff

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Updating results… 10 Contract jobs

Global Labelling Lead - Regulatory Affairs

Posted Today by Hays


Your new companyWe are currently seeking an experienced Global Labelling Lead to join a leading global biopharmaceutical...

  • Rate £90 per hour
  • Category Not specified
  • Work type Hybrid
  • Location Maidenhead

Global Labelling Lead - Regulatory Affairs

Posted Today by Hays


Your new companyWe are currently seeking an experienced Global Labelling Lead to join a leading global biopharmaceutical...

  • Rate £90 per hour
  • Category Not specified
  • Work type Hybrid
  • Location Maidenhead (SL6), SL6

Regulatory Affairs Director Contract - Execution team

Posted Today by Hays


About the RoleI am supporting an Oncology biotechnology organisation seeking an experienced Regulatory Affairs leader to...

  • Rate Not specified
  • Category Inside
  • Work type Hybrid
  • Location City of London (EC1), EC1

Regulatory Affairs Manager

Posted Today by Orion Group


Orion Group Life Sciences are currently recruiting a Regulatory Affairs Manager on behalf of our Multinational Biopharma...

  • Rate Not specified
  • Category Outside
  • Work type Not specified
  • Location Singapore, Buona Vista

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Regulatory Affairs Associate II (CMC Regulatory Strategy and Lifecycle Managemen...

Posted 4 days ago by Orion Group


Job DescriptionThe Regulatory Affairs Associate II supports Chemistry Manufacturing and Controls regulatory activities f...

  • Rate £39 per hour
  • Category Outside
  • Work type Hybrid
  • Location United States, Illinois, North Chicago

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Regulatory Affairs Manager UK and Ire

Posted 1 week ago by Hays


Your new companyOur client, a highly regarded Regulatory Affairs consultancy, is seeking an experienced Regulatory Affai...

  • Rate £55 per hour
  • Category Outside
  • Work type Remote
  • Location Twyford, Reading (RG10)

regulatory affairs specialist - dietary supplements & food compliance

Posted 1 week ago by Randstand (USA)


Job SummaryAdvance your regulatory career with a top-tier global health and nutrition leader in a fully remote position!...

  • Rate Not specified
  • Category Outside
  • Work type Remote
  • Location saint louis, missouri (remote)

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Regulatory Affairs Specialist

Posted 1 week ago by NexInfo Solutions, Inc.


About NexinfoNexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and...

  • Rate Not specified
  • Category Outside
  • Work type Remote
  • Location Remote

Sr Regulatory Affairs Specialist

Posted 2 weeks ago by Hydrogen Group


The Regulatory Affairs Specialist is responsible for preparing and maintaining regulatory submissions and approvals for...

  • Rate Not specified
  • Category Outside
  • Work type Remote
  • Location Chicago, Illinois

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Regulatory Affairs Senior Manager

Posted 2 weeks ago by Park Street People


The Role:We are seeking an experienced Senior Regulatory Manager with strong expertise in EMA regulatory affairs to join...

  • Rate Not specified
  • Category Not specified
  • Work type Not specified
  • Location London

About Our Regulatory Affairs Contract Roles in Cardiff

What does a regulatory affairs contractor do?

Contract Regulatory Affairs engagements cover work within pharmaceutical, biotechnology, medical device, and food companies to manage the regulatory submissions, approvals, and compliance activities required to bring products to market and maintain their authorisation in each territory. The work spans preparing and submitting marketing authorisation applications to the MHRA, EMA, FDA, and other national regulatory agencies, managing the lifecycle of approved products including variations, renewals, and labelling updates, advising on the regulatory strategy for new product development programmes, and ensuring that manufacturing and quality processes meet the regulatory standards required for continued product authorisation. RA contractors are brought in to manage specific submission projects, to cover regulatory vacancies, or to provide specialist regulatory expertise in a particular region or product category.

Clients expect Regulatory Affairs contractors to bring are highly specialist and require both deep knowledge of the applicable regulatory frameworks and practical experience managing the submission process. For pharmaceutical RA roles, thorough knowledge of the ICH CTD format, the EMA and MHRA centralised and national procedure routes, and the specific requirements for variation management, annual reassessment, and renewals is expected. For medical device RA contractors, knowledge of the MDR and IVDR regulatory frameworks, the CE marking and UKCA marking processes, and the technical file requirements for class II and III devices is the primary technical requirement. Most Regulatory Affairs contractors have prior experience within a regulatory affairs function of a pharmaceutical or device company, or within a regulatory consultancy or CRO, and build their contracting career on the depth of their regulatory knowledge and submission track record.

What is the market like for regulatory affairs contractors?

The Regulatory Affairs contract market is a well-established and active and specialist market within the life sciences sector, driven by the ongoing pipeline of product development and the continuous regulatory lifecycle management requirements of approved products. The impact of Brexit on the UK regulatory landscape, including the MHRA's development of its own regulatory routes for medicines and devices, has created additional demand for RA contractors with specific MHRA expertise. The wave of new biological and ATMP products requiring first-time regulatory submissions has generated significant demand for senior RA contractors with experience in complex biological submissions. Rates for experienced Regulatory Affairs contractors, particularly those with successful NDA, MAA, or MDR submission track records, are at the premium end of the life sciences contracting market.

What is the contracting market like in Cardiff?

Devolved government makes Cardiff the administrative centre of Wales and a consistent source of programme management, policy, and digital delivery contracts. Insurance and financial services employers, several of whom have established significant operational centres in the city, provide a steady flow of IT, data, and change roles. An emerging technology sector around the city centre and Cardiff Gate business park has added software development and cloud engineering to the local mix, though volumes remain modest compared to larger English cities. The Welsh Government's investment in digital capability is a distinctive feature of the Cardiff market, creating opportunities in govtech and public service transformation that are structured and funded differently from equivalent programmes in England.

How much do regulatory affairs contractors usually earn in Cardiff?

Contract rates for regulatory affairs roles in Cardiff typically range from £405 to £720 per day, depending on the scope of the role, required expertise, and the delivery expectations of the engagement.

How many regulatory affairs vacancies in Cardiff are there on Quality Contracts?

Over the past twelve months, we have tracked over 100 regulatory affairs contract roles across the site, with Cardiff demonstrating consistent opportunities. Data reviewed up to August 2026.