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Regulatory Affairs Associate
Job summary
A healthcare innovation company is seeking a Regulatory Affairs Associate to drive regulatory strategy across medical devices, cosmetics, and food supplements. The ideal candidate must hold a BSc/MSc in Life Sciences or related field and have a strong grasp of UK/EU regulations. Responsibilities include implementing regulatory strategies, maintaining documentation for EMEA compliance, and supporting new product launches. The role is hybrid, requiring two days onsite a week in Chippenham. Competitive salary and professional growth opportunities are offered.
Qualifications
- Strong understanding of UK/EU medical device, cosmetics, and food supplement regulations.
- Experience with regulatory dossiers, notifications, and documentation submissions.
- Working knowledge of QMS processes and compliance activities.
Responsibilities
- Implement regulatory strategies to support product compliance and commercial success.
- Support launches of innovative new products.
- Maintain and submit regulatory documentation and ensure EMEA portfolio compliance.
- Keep internal records aligned with REACH and UK REACH requirements.
- Lead QMS activities and provide regulatory guidance across teams.
- Represent the company in regulatory forums and industry discussions.
Skills
Education
Location: Chippenham, 2 days a week onsite (Hybrid)
Contract: Permanent
Are you passionate about healthcare innovation and regulatory excellence? Alliance is looking for a Regulatory Affairs Associate (known internally as a Regulatory Scientist) to join our Global Innovation and Scientific Affairs team and drive regulatory strategy across medical devices, cosmetics, and food supplements.
At Alliance, we specialise in advanced skincare solutions (KeloCote, Hydomol, and more) and vitamins, minerals & supplements (MacuShield, Forceval & Amberen….) Backed by innovation and driven by purpose, we're on an exciting journey of transformation and commercial acceleration
You’ll be the go-to expert ensuring our products meet global regulatory standards, supporting innovation, and helping our business thrive in compliance with regulations. From maintaining medical device records in EUDAMED to advising cross-functional teams on regulatory strategy, your expertise will make an impact.
- Implement regulatory strategies to support product compliance and commercial success.
- Support launches of innovative new products.
- Maintain and submit regulatory documentation and ensure EMEA portfolio compliance.
- Keep internal records aligned with REACH and UK REACH requirements.
- Lead QMS activities and provide regulatory guidance across teams.
- Represent Alliance in regulatory forums and industry discussions.
- BSc/MSc in Life Sciences, Nutrition, Food Science, Pharmacy, Chemistry, or related field.
- Strong understanding of UK/EU medical devices, cosmetics, and food supplement regulations; global exposure a plus.
- Experience with regulatory dossiers, notifications, and documentation submissions.
- Working knowledge of QMS processes and compliance activities.
- Excellent regulatory writing and documentation management skills.
- Proven ability to guide teams through regulatory challenges and support new product launches.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.