Regulatory Affairs Specialist Jobs in Selfridge, MI
RN Clinical Regulatory Compliance Specialist
- Southfield, MI (24 miles from Selfridge, MI)
- 45+ days ago
- Southfield, MI (24 miles from Selfridge, MI)
- 45+ days ago
This is a corporate position with primary work supporting Clinical Compliance, Accreditation and Regulatory Compliance at Corewell Health Grosse Pointe and Farmington Hills Hospitals. About...
- Auburn Hills, MI (24 miles from Selfridge, MI)
- 60+ days ago
- Auburn Hills, MI (24 miles from Selfridge, MI)
- 60+ days ago
Conduct internal audits to assess adherence to operational and regulatory standards. Prepare for and support external audits by regulatory bodies or third-party organizations....
Regulatory Compliance Specialist - Full Time - Pharmacy Advantage
- Rochester Hills, MI (19 miles from Selfridge, MI)
- 60+ days ago
- Rochester Hills, MI (19 miles from Selfridge, MI)
- 60+ days ago
Join Henry Ford Health Pharmacy Advantage team as a Full Time Regulatory Compliance Specialist and help support the regulations team. An exciting opportunity for candidates with a strong pharmacy...
- Detroit, MI (20 miles from Selfridge, MI)
- 90+ days ago
- Detroit, MI (20 miles from Selfridge, MI)
- 90+ days ago
City of Detroit Construction and Demolition Department The Program Analyst III - Community Development Specialist III is an experienced-level professional located within the City of Detroit...
Demographic Data for Selfridge, MI
Moving to Selfridge, MI? Find some basic demographic data about Selfridge, MI below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Selfridge, MI
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Selfridge, MI 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
- Regulations
- Bachelor's Degree
- Policy Development
- Microsoft PowerPoint
- 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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