Medical Device Regulatory Affairs Development (RAD) Program (on-site)
Abbott Laboratories(4 days ago)
About this role
Abbott offers a role within their Medical Device Regulatory Affairs Development Program, providing rotation-based experience in regulatory submission processes, compliance, and communication with regulatory agencies. The position supports global product registration activities and ensures adherence to international regulations in a dynamic healthcare environment.
Required Skills
- Regulatory Affairs
- Medical Devices
- Regulatory Submission
- FDA Regulations
- International Regulations
- Documentation
- Quality Systems
- Regulatory Compliance
- Product Launch
- Medical Industry
About Abbott Laboratories
abbott.comInnovative medical devices and health care solutions for cardiovascular health, diabetes management, diagnostic testing, nutrition, chronic pain and more.
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