Duration
12 months
Job Description
The client is looking for a Regulatory Operations/Submissions Consultant. This individual will be working with Class I medical devices; Specimen, Swabs, Q-Tips. The products are not complex and are not sold over the counter. The perfect candidate has 10-12 years experience working in medical device environments. They will need to get the past due sterile medical devices certified and ready for EU submission. Coming from a Regulatory Operations background is important to give guidance on the work but also be hands on when handling day to day tasks. Looking for a go-getter and responsive individual.
Skills
- Regulatory Operations
- Regulatory Submissions
- Medical Device (Class I Products)
- EUMDR – Plus
Education
- Experience outweighs degree
Remote: Regulatory Consultant (231807)
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