Regulatory Affairs Contract Jobs in Sheffield

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Updating results… 11 Contract jobs sorted by:
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Updating results… 11 Contract jobs

Regulatory Affairs Associate I - Skincare Labeling and Global Cosmetic OTC Compl...

Posted 3 days ago by Orion Group


Job DescriptionThe Regulatory Affairs Associate I supports the development and implementation of global regulatory strat...

  • Rate £27 per hour
  • Category Outside
  • Work type Hybrid
  • Location United States, California, Irvine

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Regulatory Affairs Associate II - Medical Device global submissions, license ren...

Posted 7 days ago by Orion Group


ResponsibilitiesPrepares device regulatory strategies that enable first pass approvals under limited management supervis...

  • Rate £35 per hour
  • Category Outside
  • Work type Hybrid
  • Location United States, California, Irvine

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Regulatory Affairs Associate

Posted 1 week ago by Medinext Global LLC


Must have Skills/AttributesFDALabelingRegulatory AffairsSOPPosition DescriptionRequired Education-Bachelor's degree or c...

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

global regulatory affairs specialist - medical devices (remote)

Posted 1 week ago by Randstand (USA)


Job SummaryLaunch your career with a leading global medical device organization as a Regulatory Affairs Associate I.This...

  • Rate Not specified
  • Category Outside
  • Work type Remote
  • Location deerfield, illinois (remote)

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Project Manager - Regulatory Affairs

Posted 1 week ago by Techridge, Inc.


Job DescriptionLead global registration, re-registration, renewal, and lifecycle management activities across internatio...

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

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Project Manager - Regulatory Affairs(Only Independent Candidates)

Posted 1 week ago by Sidzen LLC


Top 4 Must-Have SkillsGlobal Regulatory Affairs Experience (8+ years)Product Registrations, Re-registrations & Renew...

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

Global Labelling Lead - Regulatory Affairs

Posted 2 weeks ago 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 2 weeks ago 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 2 weeks ago 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 2 weeks ago 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 2 weeks 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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About Our Regulatory Affairs Contract Roles in Sheffield

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 Sheffield?

Advanced manufacturing and engineering research, linked to the University of Sheffield and surrounding firms, give the city a specialist contractor niche that sets it apart from its Yorkshire neighbour Leeds. Engineering, materials science, and technical project management roles generated by this cluster are difficult to replicate elsewhere in the north of England. NHS trusts serving South Yorkshire are substantial employers across clinical systems, operational improvement, and IT. A smaller but visible digital and technology community around the city centre is adding development, data, and design work year on year. Many contractors operate across both Sheffield and Leeds, treating the two as a single market. For those with engineering or manufacturing backgrounds, Sheffield offers a concentration of relevant opportunity that larger cities often lack.

How much do regulatory affairs contractors usually earn in Sheffield?

Contract rates for regulatory affairs roles in Sheffield 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 Sheffield are there on Quality Contracts?

Over the past twelve months, we have tracked over 100 regulatory affairs contract roles across the site, with Sheffield showing regular listings. Data reviewed up to September 2026.