Medical Device Company jobs in Cambridge

We are looking to add talented Regulatory Affairs professionals to our database for future contract opportunities. These roles could support the delivery of regulated products and services, with scope to manage compliance across product lifecycles and stakeholder engagement.

Please note the content of this advert does not represent a live vacancy.

About the opportunity

This is an opportunity to register your interest in future Regulatory Affairs contract roles, working within highly regulated industries where compliance expertise shapes product success. Roles of this type could sit within organisations advancing medical devices, pharmaceuticals or other regulated sectors toward market approval and post-launch compliance. The work could involve partnering across quality, engineering and commercial teams to keep programmes compliant with evolving regulatory frameworks, with scope to influence how products are positioned to regulators and markets.

Typical role overview

• Location: Cambridge, Cambridgeshire, England
• Type: Contract · Full-time
• Rate: £450–550 per day
• Domain: Regulatory Affairs · Medical Device / Regulated Industries

What you would do

Typical responsibilities could include:

• Managing regulatory submissions and dossier preparation for product launches
• Ensuring compliance with ISO 13485, IEC 62304 and relevant Class III medical device standards
• Liaising with regulatory bodies on behalf of the business and managing approval timelines
• Coordinating cross-functional teams to maintain regulatory strategy throughout the product lifecycle
• Supporting post-market surveillance and change control processes
• Advising on regulatory risk and maintaining audit readiness
• Monitoring regulatory landscape changes and updating compliance frameworks

What you could bring

Most roles of this type require the following:

• Bachelor's degree in Business or related discipline
• Demonstrable experience in regulatory affairs, compliance or quality assurance
• Working knowledge of ISO 13485, IEC 62304 and Class III medical device regulations
• Strong stakeholder management and written communication skills
• Familiarity with regulatory submissions and dossier management
• Preferred: Certified Compliance Professional (CCP) or equivalent regulatory certification
• Authorization to work in the United Kingdom

What roles of this type could offer

Most roles of this type offer the following, dependent on the industry and seniority of the role:

• The opportunity to influence how regulated products reach the market
• Exposure to complex compliance frameworks and regulatory strategy
• Scope to develop expertise in a specialised, high-value discipline
• Contract flexibility and competitive daily rates
• Potential for extension and conversion to permanent roles where performance and business needs align
• Professional development opportunities within a growing specialist consultancy

About SThree

SThree is the global STEM workforce consultancy.
We advise businesses, build expert teams and deliver project solutions to outpace tomorrow, together.

Across the UK, we connect talented specialists with cutting-edge opportunities across technology, engineering, life sciences and financial services supported by our offices in London, Birmingham, Manchester, Glasgow and Leeds

How to register interest

If you are interested in being added to our database to be considered for future opportunities, registering is quick and easy. No cover letter required. We will be in touch when we are instructed on these roles to discuss the next step in your career.

Disclaimer:
Please note that the content of this advert does not represent a live vacancy or any guarantee of future vacancies, and by responding to this advert you agree to us adding your details to our database for future opportunities.