Regulatory Affairs Specialist Jobs in Warwick, RI
Principal Regulatory Affairs Specialist
- Mansfield, MA (24 miles from Warwick, RI)
- 5 days ago
- Mansfield, MA (24 miles from Warwick, RI)
- 5 days ago
A Day in the Life As a Principal Regulatory Affairs Specialist at Medtronic, you will play a critical role in shaping the global regulatory strategy for innovative medical technologies....
Senior Financial Compliance Analyst Brown University
- Providence, RI (8 miles from Warwick, RI)
- 22 days ago
- Providence, RI (8 miles from Warwick, RI)
- 22 days ago
The incumbent participates in initiatives with partner offices at the University, including Controller, OIT/ Workday Program, Corporate & Foundation Relations, and Internal Audit....
Senior Financial Compliance Analyst
- Providence, RI (8 miles from Warwick, RI)
- 23 days ago
- Providence, RI (8 miles from Warwick, RI)
- 23 days ago
The incumbent participates in initiatives with partner offices at the University, including Controller, OIT/ Workday Program, Corporate & Foundation Relations, and Internal Audit....
Staff Regulatory Affairs Specialist - BD Excellence
- Warwick, RI
- 30+ days ago
- Warwick, RI
- 30+ days ago
Responsibilities include: Write drug and medical device regulatory submissions including NDA, ANDA, Prior Approval Supplements (PAS), Changes Being Effected (CBE), PMA supplements, 510(k)s, and Regulatory...
Demographic Data for Warwick, RI
Moving to Warwick, RI? Find some basic demographic data about Warwick, RI below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Warwick, RI
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Warwick, RI 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
- Annuities
- 21 CFR 820
- ISO 13485
- Validation
- Medical Device Sales
- Microsoft Visio
- Corrective Actions & Preventive Actions
- FDA Regulations
- Resolution
- Root Cause Analysis
- Standard Operating Procedures
- Continuous Improvement
- Product Development
- Reimbursement
- Vendor Management
- Risk Management
- Engineering
- Implementation
- Military Background
- Written Communication
- Analytical Skills
- Auditing
- Process Improvement
- Microsoft Outlook
- Documentation
- Verbal Communication
- Collaboration
- Interpersonal Skills
- Investigation
- Reporting
- Education Experience
- Policy Development
- Regulations
- Microsoft PowerPoint
- Filing
- Bachelor's Degree
- Project Management
- Time Management
- Research Skills
- Microsoft Office
- Microsoft Excel
- Sales
- Computer Skills
- Staff Supervision
- Organization
- Problem Solving
- Scheduling
- Leadership
- Communication Skills
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