At a Glance
- Tasks: Lead regulatory activities for innovative medical devices and collaborate with global teams.
- Company: Join a globally recognised leader in the medical device industry.
- Benefits: Competitive salary, career growth, and the chance to work on cutting-edge technologies.
- Other info: Dynamic role focused on technical ownership and cross-functional collaboration.
- Why this job: Make a real impact by bringing new medical devices to market across Europe.
- Qualifications: Proven experience in Regulatory Affairs within the Medical Device sector and knowledge of MDR 2017/745.
The predicted salary is between 55000 - 65000 £ per year.
Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a strong international presence and continued investment into next-generation technologies, the business is continuing to expand its regulatory capability across high-profile product programmes.
We have an opportunity for a Principal Regulatory Affairs Specialist to join the organisation and support the development and approval of a brand new medical device programme under MDR 2017/745. Working as part of a highly experienced global Regulatory Affairs function, this role will play a key part in helping bring an innovative new product to market across Europe.
The position is centred around technical Regulatory Affairs ownership and cross-functional project leadership rather than people management. You will work closely with R&D, Clinical and global Regulatory teams throughout the product development lifecycle, supporting regulatory activities from early-stage development through to submission and approval. Alongside this, you will contribute to the regulatory strategy for the programme, helping define approval pathways, manage regulatory risk and support interactions with Notified Bodies and Competent Authorities.
To be successful as the new Principal Regulatory Affairs Specialist, you will have proven Regulatory Affairs experience within the Medical Device sector alongside strong working knowledge of MDR 2017/745. You will have experience supporting new product development activities, contributing to regulatory submissions and operating within cross-functional product development environments.
- Support the development and approval activities for a new medical device programme under MDR 2017/745.
- Work closely with global Regulatory Affairs, Clinical Affairs and R&D teams across the product development lifecycle.
- Contribute to regulatory strategy activities and support the definition of EU approval pathways.
- Develop and maintain regulatory plans aligned to product development and submission milestones.
- Provide regulatory input into technical documentation, risk management and clinical activities.
Proven Regulatory Affairs experience within the Medical Device sector.
- Strong working knowledge of MDR 2017/745 and associated regulatory frameworks.
- Experience supporting regulatory activities for medical device development programmes.
- Experience contributing to regulatory submissions and technical documentation activities.
- Experience with Class III medical devices, combination products or drug-device products would be advantageous but is not essential.
- Degree qualified within a scientific, engineering or related discipline.
This is an opportunity to join a globally recognised medical device organisation working on a high-profile development programme where Regulatory Affairs sits at the centre of product development and market approval activities. If you enjoy technically focused Regulatory Affairs work, collaborative project environments and supporting innovative products through to market launch, please get in touch with Kris Holmes today or click apply now.
Medical Device Regulatory Affairs Specialist in Oxford employer: Cure Talent
As a leading global medical device organisation, we pride ourselves on fostering a dynamic and inclusive work culture that prioritises innovation and collaboration. Our employees benefit from extensive professional development opportunities, competitive compensation packages, and the chance to work on groundbreaking projects that make a real difference in healthcare. Join us in our state-of-the-art facilities, where your expertise in Regulatory Affairs will be valued and your contributions will directly impact the future of medical technology across Europe.
StudySmarter Expert Advice🤫
We think this is how you could land Medical Device Regulatory Affairs Specialist in Oxford
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We think you need these skills to ace Medical Device Regulatory Affairs Specialist in Oxford
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Cure Talent!
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How to prepare for a job interview at Cure Talent
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Cure Talent that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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