Regulatory Affairs Specialist
RandstadRaleigh, NC, USjob_description.job_card.variable_days_ago
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Regulatory Affairs Specialist
Raleigh client seeking contractor for onsite Regulatory Affairs Specialist, M-F. The Regulatory Affairs Specialist will be responsible for supporting regulatory activities for existing US FDA class III medical devices. This role provides support to currently-marketed products, involves evaluating proposed product and process changes, assessing documentation and providing guidance to ensure regulatory compliance. The Regulatory Affairs Specialist will :
- Support Regulatory Activities
- Evaluate Proposed Product and Process Changes
- Assess Documentation
- Provide Guidance to Ensure Regulatory Compliance
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Regulatory Specialist • Raleigh, NC, US
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