Principal Regulatory Affairs Specialist (m/f/d)
LivaNova(23 days ago)
About this role
A Principal Regulatory Affairs Specialist at LivaNova is a senior regulatory professional focused on ensuring medical device products meet global regulatory and clinical standards across their lifecycle. The role provides regulatory expertise to support market access and regulatory strategy in international markets, working closely with clinical, quality, and product teams.
Required Skills
- Regulatory Submissions
- Clinical Trials
- Technical Writing
- Regulatory Compliance
- Quality Systems
- Cross-Functional Collaboration
- Project Management
- Time Management
- Stakeholder Management
- MS Office
Qualifications
- BS in Engineering
- BS in Life Sciences
- BS in Pharmacy
- BS in Nursing
- BS in Mathematics/Statistics
- MS (Preferred)
- PhD (Preferred)
About LivaNova
livanova.comLivaNova is a global medical device company creating neuromodulation devices and cardiopulmonary products to improve the lives of patients worldwide.
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