Regulatory Affairs Specialist II – Cardiac Rhythm Management (on-site)
Abbott Laboratories(1 month ago)
About this role
A Regulatory Affairs Specialist II at Abbott's Cardiac Rhythm Management division supports worldwide regulatory registration for medical devices, preparing and submitting documentation to ensure compliance with FDA and international agency requirements. The role is based on-site in Sylmar, CA and contributes to product market entry and regulatory strategy within a global healthcare company.
Required Skills
- Regulatory Submissions
- Technical Writing
- FDA Regulations
- EU Regulations
- Quality Management
- Cross-Functional
- Project Management
- Communication Skills
- Attention To Detail
Qualifications
- Bachelor's Degree
- Master's Degree
- Regulatory Affairs Professionals Society Certification
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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