Regulatory Affairs Specialist Jobs in Waverly, MN
Regulatory Affairs Specialist II - Interventional Cardiology (Hybrid)
- Maple Grove, MN (23 miles from Waverly, MN)
- 1 day ago
- Maple Grove, MN (23 miles from Waverly, MN)
- 1 day ago
As a Regulatory Affairs Specialist II, you will support a broad range of Interventional Cardiology devices, with an emphasis on sustaining commercial products and executing regulatory submissions for...
Senior Regulatory Affairs Specialist
- Maple Grove, MN (23 miles from Waverly, MN)
- 23 days ago
- Maple Grove, MN (23 miles from Waverly, MN)
- 23 days ago
About the role: We are looking to hire an enthusiastic individual for a Senior Regulatory Affairs Specialist position supporting exciting sources of growth for Boston Scientific....
Principal Regulatory Affairs Specialist
- Maple Grove, MN (23 miles from Waverly, MN)
- 60+ days ago
- Maple Grove, MN (23 miles from Waverly, MN)
- 60+ days ago
/supporting a variety of regulatory submissions for US and EU, such as IDEs, pre-submissions, original PMAs, PMA Supplements, 510(k)s, and MDR Technical Documentation Basic submission and presentation...
Regulatory Affairs Specialist - Medical Devices
- Maple Grove, MN (23 miles from Waverly, MN)
- 90+ days ago
- Maple Grove, MN (23 miles from Waverly, MN)
- 90+ days ago
Reporting to the Director of Regulatory Affairs, the Regulatory Affairs Specialist will lead and execute regulatory submission and approval activities for the company's medical device products, with...
Demographic Data for Waverly, MN
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Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Waverly, MN
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Waverly, MN offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Regulatory Affairs Specialist position
- Internal Audits
- ICH Guidelines
- 21 CFR 820
- Institutional Review Board
- ISO 13485
- Quality Systems
- Quality Management Systems
- Validation
- Medical Device Sales
- Microsoft Visio
- FDA Regulations
- Corrective Actions & Preventive Actions
- Root Cause Analysis
- Microsoft SharePoint
- Standard Operating Procedures
- Product Development
- Strategy Development
- Reimbursement
- Risk Management
- Engineering
- Military Background
- Analytical Skills
- Written Communication
- Implementation
- Auditing
- Process Improvement
- Microsoft Outlook
- Documentation
- Verbal Communication
- Collaboration
- Interpersonal Skills
- Investigation
- Reporting
- Bachelor's Degree
- Policy Development
- Microsoft PowerPoint
- Regulations
- Filing
- Education Experience
- Project Management
- Time Management
- Research Skills
- Microsoft Office
- Sales
- Computer Skills
- Staff Supervision
- Microsoft Excel
- Problem Solving
- Scheduling
- Leadership
- Communication Skills
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