What are the responsibilities and job description for the Regulatory Affairs Specialist position at QuinTalent Inc?
This 6 months position will perform international registration for medical diagnostic equipment.
Administrative duties in Trackwise digital database
Respond to incoming requests for international registrations and provide country registration documentation according to schedule.
Work with regulatory specialist team to learn and provide primary documentation that is required for each country registration worldwide.
Update project team on current status of registration for medical devices.
- Demonstrated ability to work with individuals at all levels, both internal and external to the organization.
- Demonstrated ability to adjust to multiple priorities; proven ability to work independently
- Ability to prioritize tasks and exercise good judgment; excellent attention to detail and the ability to produce work with a high level of accuracy.
- Experience with word, excel and Document Control in a regulated environment.
Job Type: Contract
Pay: $45.00 - $50.00 per hour
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Hercules, CA 94547: Reliably commute or planning to relocate before starting work (Required)
Experience:
- FDA regulations: 3 years (Required)
- Regulatory reporting: 3 years (Required)
Work Location: One location
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