RA Med Dev - Hertfordshire - GBP40K
A Global Medical Device client of mine is currently looking for a Regulatory Consultant to join them on a contract basis at their site in Hertfordshire.
- Risk Management
- Change Control
- SOP Writing
- STED Documentation
- Technical Files for CE Marking
- 4+ years Regulatory experience in the Medical Device industry
- Experience working with Class I, IIa, IIb, III Medical Devices
- EU Product Registrations
- Excellent verbal and written communication skills
- Excellent interpersonal skills
Job Type: Permanent
If you are interested in this position or know anyone who might be please get in touch ASAP with an up to date CV and I'll be in touch immediately to discuss setting up an interview.