Regulatory Affairs Specialist - Medical Devices - London
We have been mandated by a growing medical devices company in London to find an experienced regulatory affairs and quality assurance specialist to join their team.
You will be a key member of this fledgling team, working closely with people throughout the business, to ensure the product meets strict regulatory criteria as well as quality assurance standards and internal audits. This will involve setting up new processes and strategies that will be company-wide.
This company recently moved into new offices and have a plan for the company's growth and success. As the company grows, you will get the opportunity to take on more responsibility, something that is not often available at most companies. The company are essentially looking for an associate/specialist who is looking to move into a management role as they grow.
The company have developed a ground-breaking product, which is unrivalled within their space, meaning this could be a great opportunity to get involved with a technology that is a genuine step-change forward.
It is understood that you would most likely hold a degree within an engineering, design, medical or life sciences background, however the industry exposure is more important than your education, for this role. You will need to have experience with ISO 13485, using a quality management system and ideally, internal audits.
You will be rewarded with a challenging role that you will never get bored with. The company are offering competitive salaries as well as share options, pension, and the usual benefits.
For more information, please feel free to call Matthew Lowdon, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on 0121 268 2240 or make an application and one of our team at Newton Colmore Consulting will contact you.
Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.
Medical Devices Regulatory Affairs Specialist, RA Specialist, Regulatory Affairs Manager, Quality Assurance, ISO 13485, CE Mark, CE Marking, FDA 510k, RA Consultant, RA Manager, Regulatory Affairs Consultant
You must be eligible to work in the UK. Learn more
- Agency: Newton Colmore Consulting
- Reference: NC-TW-0577622
- Posted: 2nd September 2020
- Expires: 30th September 2020