Regulatory Operations Specialist
4 weeks ago
Regulatory Operations Specialist
This role is responsible for supporting global regulatory operations and fast impact projects. The position reports to the R&D Fellow, Neuromodulation.
Key Responsibilities:
- Administration of global processes for monitoring, control, and communication of external documents applicable to LivaNova medical devices.
- Management and leadership of cross-functional teams to develop and execute sustaining, continuous improvement regulatory compliance projects.
- Resource management with the Project Management Office to ensure programs are sufficiently resourced to meet milestones and deliverables.
Requirements:
- Bachelor's degree in engineering or science.
- Resourceful, creative, well-organized with an ability to prioritize and proactively offer solutions.
- Ability to work effectively within a team in a fast-paced changing environment.
- Excellent verbal and written communications with ability to effectively communicate at multiple levels in the organization.
Desired Skills and Qualifications:
- BS degree in related Engineering discipline.
- Knowledge and understanding of medical device related standards used medical device quality systems, and in the design, development, and distribution of medical devices.
- Significant experience working in a broader enterprise/cross functional business preferred.
Employee Benefits:
- Target Compensation Range: $100,000 - $130,000 per year plus annual bonus.
- Health benefits - Medical, Dental, Vision.
- Personal and Vacation Time.
- Retirement & Savings Plan (401K).
- Employee Stock Purchase Plan.
- Training & Education Assistance.
- Bonus Referral Program.
- Service Awards.
- Employee Recognition Program.
- Flexible Work Schedules.
LivaNova's Commitment to Diversity & Inclusion:
LivaNova values equality and celebrates diversity. We are committed to ensuring that our recruitment process is fair, transparent and free from unlawful discrimination.
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