At a Glance
- Tasks: Ensure compliance and quality assurance for innovative medical devices across multiple regions.
- Company: Dynamic medical devices company in Cambridgeshire with a focus on innovation.
- Benefits: Opportunities for growth, autonomy, and involvement in life-saving technology.
- Other info: Join a team of experts in a supportive environment that values responsibility.
- Why this job: Make a real difference in healthcare by shaping regulatory strategies and processes.
- Qualifications: Knowledge of ISO 13485, CE Marking, and experience in quality assurance.
The predicted salary is between 45000 - 55000 £ per year.
Regulatory Affairs Specialist - MedTech A growing medical devices company in Cambridgeshire are currently in need of an experienced quality assurance and regulatory affairs specialist. This is an excellent opportunity for a QARA specialist to join this team of experts and work on highly complex medical technology, across multiple territories and product ranges. This is a key role in the development of lifesaving and life-improving medical devices, ensuring compliance, assurance, and regulatory best practice across the entire design and manufacturing process on products and services that will be launched in Europe, North America, and the APAC region. This company have a proven track record of delivering step-changes in technology through innovation and intricate design, and you will fit right in if you have a sharp eye for detail and enjoy working in an environment that prioritises autonomy and responsibility. To be successful in this role you will need to have knowledge of quality assurance and regulatory standards within the UK and Europe. So, in-depth knowledge of ISO 13485, CE Marking, and other standards will be essential. This role will give you the chance to shape their strategy and processes while providing great opportunities for growth and development. Undertaking internal audits will be important in this role so hopefully you have experience of this in your...
Regulatory Affairs Specialist - MedTech + More employer: Newton Colmore Consulting Ltd
As a Mechanical Engineer in Robotics Design at this innovative start-up biotech company in London, you will be part of a dynamic team dedicated to developing cutting-edge biotechnology products. The company fosters a collaborative work culture that encourages creativity and growth, offering competitive salaries, equity options, and opportunities for professional development in a fast-paced environment. Joining this team means contributing to meaningful projects that have the potential to make a significant impact in the life sciences sector.
Contact Details:
Newton Colmore Consulting Ltd Recruitment Team
We think you need these skills to ace Regulatory Affairs Specialist - MedTech + More
Quality Assurance
Regulatory Affairs
ISO 13485
CE Marking
Internal Audits
Attention to Detail
Compliance Knowledge
