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- Tasks: Join our team as a Quality and Regulatory Specialist, ensuring compliance for medical devices.
- Company: Be part of a global leader in the Medical Device sector with innovative products.
- Benefits: Enjoy flexible hybrid work, private healthcare, dental cover, and subsidized gym membership.
- Why this job: Contribute to impactful projects in a collaborative environment while growing your career.
- Qualifications: Degree in Biomedical, Life Sciences, or Regulatory Affairs; experience in QA/RA required.
- Other info: Work from London 2 days a week, with flexibility on office days.
The predicted salary is between 36000 - 60000 £ per year.
We are supporting our client, a global player within the Medical Device sector as they expand their QA/RA team by hiring a new Quality and Regulatory Specialist to join during a continued phase of growth for the business. This role offers a very flexible and hybrid working pattern, based in our clients head office in London. This can be suitable for candidates not only based in London/surrounding counties, but also those further afield who can commute into London 2 days per week. The 2 days you work in the office are completely flexible and up to you. About the company you are joining: A global Medical Device business, who manufacture and supply a diverse range of medical device products (Class I, Class IIa and Class III) as well as non-medical device products into the UK retail and wholesale markets. Benefiting from a having a strong/core product portfolio established within the market – ranging from pain relief products to general safety products, and there are further plans to launch more new products into the market soon. About the Quality and Regulatory Specialist role:
Quality and Regulatory Specialist - Medical Devices employer: Radar Recruitment Careers
Contact Detail:
Radar Recruitment Careers Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality and Regulatory Specialist - Medical Devices
✨Tip Number 1
Make sure to familiarize yourself with ISO 13485 standards and the Medical Device Regulation (MDR). Having a solid understanding of these regulations will not only help you in interviews but also demonstrate your commitment to quality and regulatory compliance.
✨Tip Number 2
Network with professionals in the medical device industry, especially those working in Quality Assurance and Regulatory Affairs. Attend relevant conferences or webinars to connect with potential colleagues and learn more about the latest trends and challenges in the field.
✨Tip Number 3
Prepare to discuss your experience with complaint handling and post-market surveillance during the interview. Be ready to share specific examples of how you've managed complaints and contributed to continuous improvement in previous roles.
✨Tip Number 4
Highlight your adaptability and collaborative skills in conversations with our team. This role requires working closely with various departments, so showcasing your ability to work well with others will set you apart from other candidates.
We think you need these skills to ace Quality and Regulatory Specialist - Medical Devices
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your experience in Quality Assurance or Regulatory Affairs within the Medical Device sector. Use specific examples that demonstrate your knowledge of ISO 13485 standards and Medical Device Regulation (MDR).
Showcase Your Educational Background: Clearly state your degree in a Scientific discipline, such as Biomedical or Life Sciences. This is crucial for demonstrating your qualifications for the role.
Tailor Your CV and Cover Letter: Customize your CV and cover letter to reflect the key responsibilities and skills mentioned in the job description. Highlight your adaptability and collaborative spirit, as these traits are valued by the company.
Prepare for Technical Questions: Be ready to discuss your familiarity with Post-Market Surveillance, Vigilance Reporting, and other relevant processes during the interview. Prepare examples of how you've handled complaints and contributed to risk assessments.
How to prepare for a job interview at Radar Recruitment Careers
✨Show Your Knowledge of ISO 13485
Make sure to highlight your understanding of ISO 13485 standards during the interview. Be prepared to discuss how you've applied these standards in your previous roles, as this will demonstrate your expertise and relevance for the Quality and Regulatory Specialist position.
✨Prepare for Technical Questions
Expect technical questions related to Quality Management Systems and regulatory compliance. Brush up on your knowledge of Medical Device Regulation (MDR) and be ready to provide examples of how you've handled compliance issues or audits in the past.
✨Demonstrate Your Problem-Solving Skills
Since complaint handling and post-market surveillance are key responsibilities, prepare to discuss specific instances where you've successfully resolved complaints or contributed to continuous improvement initiatives. This will showcase your proactive approach and problem-solving abilities.
✨Emphasize Collaboration
The role requires working collaboratively with various teams. Share examples of how you've effectively collaborated with colleagues from different departments, highlighting your adaptability and communication skills. This will show that you're a team player who can thrive in a hybrid working environment.
