Senior Regulatory Affairs Associate Jobs UK 2026 – Cambridge, England

Senior Regulatory Affairs Associate Jobs UK offer a potential career opportunity for experienced pharmaceutical and life-sciences professionals seeking to advance their careers in regulatory affairs. A world-leading biopharmaceutical organisation is advertising a Senior Regulatory Affairs Associate position supporting regulatory activities across the United Kingdom and Ireland.

According to the supplied vacancy details, the position is based in Cambridge, England, and was advertised by Hays Specialist Recruitment. The opportunity is described as a contract role with hybrid working arrangements, including three days of remote work as indicated in the advertisement.

The role focuses on regulatory submissions, product lifecycle management, labelling, regulatory documentation, and compliance with applicable UK and Irish requirements. Candidates with pharmaceutical regulatory experience, strong technical writing skills, and knowledge of regulatory procedures may find this opportunity worth exploring.

The vacancy was published on 18 September 2026, with a stated closing date of 18 October 2026. Applicants should verify the current status and full selection criteria through the official job listing before applying.

 

Job Overview

• Job Title: Senior Regulatory Affairs Associate
• Job Category: Regulatory Affairs
• Industry: Pharmaceutical and Biopharmaceutical
• Location: Cambridge, England, United Kingdom
• Geographical Scope: UK and Ireland
• Employer/Recruiter: Hays Specialist Recruitment
• Employment Type: Contract
• Work Arrangement: Hybrid
• Remote Work: Three days per week, according to the supplied advertisement
• Advertised Salary: £27–£30 per hour
• Publication Date: 18 September 2026
• Closing Date: 18 October 2026
• Application Source: UK Government job listing
• Application Link: View the official job listing

About the Opportunity

Regulatory affairs plays an essential role in the pharmaceutical industry by helping ensure that medicines meet applicable regulatory requirements throughout their development, approval, manufacture, and commercial lifecycle.

The Senior Regulatory Affairs Associate Jobs UK opportunity is aimed at experienced professionals who can support regulatory activities across the UK and Ireland. The successful candidate is expected to contribute to submission preparation, product maintenance activities, labelling documentation, and regulatory compliance.

Working in a regional regulatory role requires attention to detail, effective communication, and the ability to coordinate information across different departments. Regulatory affairs professionals often collaborate with quality assurance, clinical, medical, manufacturing, supply chain, and other teams to ensure that submissions and product information remain accurate and up to date.

This position may be suitable for candidates who already understand pharmaceutical regulatory documentation and want to build further experience in a biopharmaceutical environment.

Key Responsibilities of a Senior Regulatory Affairs Associate

1. Regulatory Strategy and Product Lifecycle Management

The successful candidate will support regulatory strategies and product lifecycle activities across the UK and Ireland.

These activities may include maintaining existing product authorisations, coordinating regulatory changes, and helping ensure that product information remains aligned with applicable regulatory requirements.

Lifecycle management is important because medicines may require regulatory updates following changes to manufacturing processes, product information, approved indications, or other relevant aspects of their authorisation.

2. Preparation and Coordination of Regulatory Submissions

A key responsibility will be preparing and coordinating regulatory submissions in accordance with established processes and timelines.

The work may involve collecting information from internal departments, checking documentation for completeness, coordinating submission components, and supporting the preparation of regulatory responses.

Candidates should understand the importance of accurate submission documentation, version control, and timely communication when managing regulatory deliverables.

3. Product Labelling and Regulatory Documentation

The role includes assisting with product labelling and regulatory documentation.

Pharmaceutical labelling must remain consistent with the applicable authorised product information and relevant regulatory requirements. Updates may require coordination with medical, quality, safety, and other internal stakeholders.

The successful candidate should have strong documentation skills and an ability to review technical information carefully.

4. UK and Irish Regulatory Compliance

The Senior Regulatory Affairs Associate Jobs UK position involves supporting compliance with relevant regulatory requirements in the UK and Ireland.

Candidates should be familiar with the importance of maintaining accurate regulatory records, monitoring applicable requirements, and ensuring that product-related activities follow established regulatory procedures.

Applicants should confirm which specific regulatory frameworks and product categories are covered by the employer’s portfolio.

5. Coordination with Internal Teams and Regulatory Agencies

Regulatory affairs professionals work closely with cross-functional teams to obtain information, resolve documentation queries, and coordinate regulatory activities.

The role may also involve supporting interactions with regulatory agencies, preparing responses to requests, and tracking outstanding regulatory commitments.

Clear written communication and the ability to manage several activities simultaneously are valuable for this type of position.

6. Submission Tracking and Record Management

The successful candidate will track regulatory submission timelines and maintain accurate regulatory records.

Effective tracking helps teams monitor submission milestones, identify potential delays, and ensure that required documentation is available when needed.

Maintaining reliable records also supports inspection readiness and helps demonstrate compliance with applicable internal procedures.

Qualifications and Experience

Candidates interested in Senior Regulatory Affairs Associate Jobs UK should have relevant experience in pharmaceutical, biopharmaceutical, or life-sciences regulatory affairs.

The supplied advertisement does not provide a complete list of mandatory qualifications. Applicants should confirm the precise requirements with Hays Specialist Recruitment.

Relevant educational backgrounds may include:

• Bachelor’s degree in Pharmacy.
• Master’s degree in Pharmacy.
• Pharmaceutical Sciences.
• Life Sciences or Biological Sciences.
• Another relevant scientific discipline.

Relevant professional experience may include regulatory submissions, product lifecycle management, labelling updates, regulatory documentation, and coordination of cross-functional activities.

Essential Skills for Regulatory Affairs Professionals

Applicants should highlight the following competencies where they reflect their actual experience:

• Understanding of pharmaceutical regulatory affairs.
• Experience supporting regulatory submissions.
• Knowledge of product lifecycle management.
• Strong technical writing and documentation skills.
• Familiarity with pharmaceutical labelling requirements.
• Ability to track submission timelines and regulatory commitments.
• Excellent organisational and project coordination skills.
• Strong written and verbal communication.
• Attention to detail and document version control.
• Ability to work with multiple internal stakeholders.

Experience supporting regulatory activities across the UK and Ireland may be particularly relevant to this position.

Salary and Working Arrangements

The supplied advertisement lists a salary of £27–£30 per hour for this contract opportunity.

The position is described as hybrid, with three days of remote work indicated in the listing. Applicants should confirm the precise office attendance requirements, contract duration, expected working hours, and whether the advertised hourly rate is inclusive of any applicable agency arrangements.

The actual employment terms should be confirmed with the recruiter before accepting an offer.

How to Apply for Senior Regulatory Affairs Associate Jobs UK

Interested candidates can follow these steps:

1. Visit the UK Government job listing.
2. Check whether the vacancy is still accepting applications.
3. Review the full job description and confirm the essential selection criteria.
4. Prepare an updated CV highlighting regulatory submissions, product lifecycle management, labelling, and compliance experience.
5. Include examples of relevant regulatory documentation and cross-functional coordination in your application.
6. Follow the application instructions provided in the official listing or by Hays Specialist Recruitment.
7. Confirm the contract terms, hourly rate, hybrid arrangements, and any eligibility requirements with the recruiter.

Apply Jobs

Important: The advertised closing date is 18 October 2026. As this date is approaching, candidates should check the listing promptly to confirm that the application process remains open.

Who Should Apply?

This opportunity may suit experienced Regulatory Affairs Associates, Senior Regulatory Affairs Associates, Regulatory Affairs Specialists, and pharmaceutical professionals with relevant UK and Irish regulatory experience.

Candidates should demonstrate their ability to prepare accurate documentation, coordinate submission activities, manage deadlines, and work effectively with internal stakeholders.

Applicants should ensure that their CV accurately reflects their qualifications and professional experience. Work authorisation and any additional eligibility requirements should be confirmed before applying.

Final Thoughts

The Senior Regulatory Affairs Associate Jobs UK opportunity in Cambridge may be attractive to professionals seeking contract-based regulatory affairs work in the biopharmaceutical sector.

With responsibilities covering submissions, product lifecycle management, labelling, and regulatory compliance, the position could suit candidates with strong technical documentation and coordination skills.

Review the official vacancy, confirm its current status, and submit your application according to the recruiter’s instructions.

For more UK pharmaceutical jobs, regulatory affairs vacancies, quality assurance positions, and international pharmaceutical career updates, visit Pharmaguidances.com regularly.