Regulatory Affairs Specialist Jobs in Boca Raton, FL
Kforce has a client that is seeking a Compliance Analyst in Boca Raton, FL. Summary:This role will manage the onboarding process for vendors providing services. This requires vetting new vendors,...
In PersonDEA Compliance Analyst - Weston, FL (HYBRID)
- Teva Pharmaceutical Industries
- Weston, FL (24 miles from Boca Raton, FL)
- 30+ days ago
- Weston, FL (24 miles from Boca Raton, FL)
- 30+ days ago
Who we are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across...
HybridRegulatory Affairs Associate III
- Teva Pharmaceutical Industries
- Weston, FL (24 miles from Boca Raton, FL)
- 45+ days ago
- Weston, FL (24 miles from Boca Raton, FL)
- 45+ days ago
Regulatory submissions: P-INDs, INDs, NDAs, ANDAs. Responding to FDA deficiency comments and preparing submission responses....
In Person- City of Lake Worth Beach
- Lake Worth, FL (18 miles from Boca Raton, FL)
- 60+ days ago
- Lake Worth, FL (18 miles from Boca Raton, FL)
- 60+ days ago
Completes Internal Audits of procedures, processes, and evidence for all applicable NERC The examples of essential functions as listed in this classification specification are not necessarily descriptive...
In PersonDemographic Data for Boca Raton, FL
Moving to Boca Raton, FL? Find some basic demographic data about Boca Raton, FL below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Boca Raton, FL
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Boca Raton, FL offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Regulatory Affairs Specialist position
- Annuities
- 21 CFR 820
- Internal Audits
- Institutional Review Board
- Good Clinical Practice
- ISO 13485
- Medical Device Sales
- Corrective Actions & Preventive Actions
- FDA Regulations
- Resolution
- Standard Operating Procedures
- Product Development
- Continuous Improvement
- Microsoft SharePoint
- Technical Writing
- Reimbursement
- Engineering
- Risk Management
- Analytical Skills
- Implementation
- Auditing
- Written Communication
- Military Background
- Collaboration
- Process Improvement
- Documentation
- Verbal Communication
- Data Analysis
- Interpersonal Skills
- Investigation
- Reporting
- Bachelor's Degree
- Policy Development
- Microsoft PowerPoint
- Filing
- Education Experience
- Project Management
- Research Skills
- Regulations
- Microsoft Office
- Time Management
- Staff Supervision
- Microsoft Excel
- Problem Solving
- Teamwork
- Scheduling
- Leadership
- Communication Skills
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