- Provides administrative support for regulatory affairs manager
- Provides RA support for change control projects and sustaining activities
- Conducts regulatory assessments and determines need for re-registration for proposed device changes, prepares internal documentation for changes not requiring re-registration (FDA, EU, OUS)
- Supports worldwide product registrations through collaboration with regulatory associates and cross-functional product team
- Responds to requests for product information by customers or other businesses
- bility to carry out the above tasks with minimal supervision
- Experience with disposable medical devices
- Experience with International registrations and renewal.
- Minimum Bachelor's degree; strongly preferred in science or engineering
- Minimum 1-3 years' experience in Regulatory Affairs in the medical device industry
- Demonstrated customer service, cross-functional collaboration, and teamwork skills
- Proven ability to manage multiple project deliverables and meet project timelines
- Effective written and verbal communication skills
- Scientific and analytical evaluation skills US FDA medical device regulations, standards, and guidance
- 21 CFR 820 - Quality System Regulation.
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