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An exciting opportunity has arisen for a Regulatory Affairs Compliance Specialist to ensure product compliance within a leading beauty-tech manufacturer. The successful candidate will focus on ensuring compliance of the beauty tech devices with the EU MDR requirements, maintaining regulatory approvals, and supporting the company's regulatory strategy in the EU.
Client Details
The company is a global beauty-tech manufacturer with exciting growth plans as they expand their portfolio through product development. They have a mid-sized team, dedicated to ensuring the quality and compliance of their range of products.
Description
- Ensuring product compliance in accordance with EU regulations.
- Monitoring regulatory changes and implementing necessary actions.
- Assisting in the development of regulatory strategies for new products.
- Liaising with external regulatory authorities.
- Providing regulatory advice and guidance to colleagues within the company.
- Contributing to the continual improvement of regulatory procedures.
- Reviewing product promotional material for regulatory compliance.
- Preparing and submitting regulatory submissions to EU authorities.
Profile
A successful Regulatory Affairs Compliance Specialist EU should have:
- A degree in Life Sciences or a related field.
- Proven experience in a regulatory affairs role within medical devices.
- Knowledge of EU regulatory requirements and procedures.
- Excellent communication and interpersonal skills.
- Strong attention to detail and problem-solving abilities.
- The ability to work under pressure and meet deadlines.
- Proficiency in English, with additional European languages being an asset
Job Offer
- A competitive salary
- A collaborative and supportive company culture.
- Opportunities for professional development and growth.
- Hybrid working
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