Job Title: Regulatory Associate (Remote)
Location: Remote, UK-based (occasional travel for meetings/training if required)
Role Summary
Working with a multi site MedTech manufacturer, we are looking to hire a Regulatory Associate. This is an opportunity for someone early in their regulatory career who has already gained hands-on experience in maintaining or creating technical documentation.
The role will focus on supporting regulatory submissions and compliance activities for medical devices, ensuring all documentation is accurate, complete, and audit-ready. You’ll work closely with senior members of the RA team and cross-functional departments to maintain high-quality standards while developing your skills in international regulatory frameworks.
Key Responsibilities
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Assist in the preparation, maintenance, and review of regulatory technical documentation (e.g., technical files, design dossiers, DHFs).
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Support updates to existing submissions to comply with MDR, UKCA, and FDA requirements.
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Collaborate with QA/RA colleagues to ensure alignment of quality and regulatory processes.
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Provide administrative and project support to senior RA staff on global submissions.
About You
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6 months to 1 year of experience in regulatory affairs.
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Exposure to technical file creation or maintenance (essential).
- Self-starter who is comfortable working remotely while collaborating effectively with a distributed team.
What’s on Offer
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Fully remote working arrangement.
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Career development with mentoring from experienced RA professionals.
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Exposure to a broad range of regulatory activities across multiple markets and products.
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Opportunity to build a strong foundation in regulatory affairs within an innovative and growing organisation.
Interested?
Apply now for more information.
