Real Staffing are currently working with a Global medical device organisation who are looking to expand its product range and capabilities. This is an exciting to join the growing team and to learn and develop your own experience.
requirements for this role are as follows:
4 years Biotechnology/Life Sciences industry experience, with a minimum of 2 years working experience in Regulatory/Quality
Experience with IVDR implementation is desirable
Working knowledge of ISO 13485 and regulatory requirements for medical devices (including IVDD 98/79/EC, FDA CFR 21 part 820, CMDR)
Working knowledge of EN ISO 14971:2012
Experience with post market surveillance activities and familiar with test methods, sampling plans and standard for the design, verification and validation of medical device products
As mentioned, this department is going through a period of growth and are looking to advance their product range and capabilities. Please reach out and apply for more information.
Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales