Description
A leading Medical Devices company is currently looking to hire a Senior Regulatory Affairs Specialist for a exiting new project based in Scotland.Job Description:
- This role will support the RA project Leads for the new blood glucose monitoring system development projects.
- Assisting in preparation of pre-market applications to regulatory agencies.
Candidate Criteria:
- Demonstrated experience working in a Regulatory Affairs role within the medical device industry
- Familiarity with medical device regulations in US and/or EU
- Excellent verbal and written communication skills
- Ability to work independently and collaboratively with minimal supervision
- Working knowledge of MS Office programs (Word, Excel, PowerPoint, Outlook) and electronic document management systems.
Key Points:
Location: Highlands (Scotland_
Rate: £35-£45 hourly
Duration: 6-12 Months
Feel free to apply if you think you are right for this role. If you would like more details please call Akeel on .