Regulatory Affairs Specialist Jobs in Memphis, TN
Job Title: Regulatory Affairs Specialist Duration: 12+ months contract Location: Cordova, TN 38018 Note: Can be Remote for non local candidates Job Summary: Preparation and review of global regulatory...
Proven track record of successful US FDA 510(k) submissions and clearances....
- Cordova, TN (16 miles from Memphis, TN)
- 3 days ago
- Cordova, TN (16 miles from Memphis, TN)
- 3 days ago
Regulatory Affairs Specialist, Cordova, TN Duration: 12 months Duties: • Preparation and review of global regulatory submissions, including US 510(k) and EU technical documentation, and support regional...
- Cordova, TN (16 miles from Memphis, TN)
- 3 days ago
- Cordova, TN (16 miles from Memphis, TN)
- 3 days ago
A Regulatory Affairs Specialist is needed for a medical technology company focused on the repair, regeneration and replacement of soft and hard tissue in the Cordova, TN area....
About Williams Sonoma DC - Memphis & Olive Branch Since it was founded in 1956, Williams - Sonoma has grown from Chuck Williams' single store in Sonoma, CA into one of the largest retailers in the...
Specialist, Regulatory Affairs and Specification Job Details Level Experienced Job Location Memphis Support Center - Memphis, TN Remote Type Fully Remote Position Type Full Time Education Level 4...
Remote WorkKnowledge of regulatory compliance requirements (e.g. 21 CFR 820, ISO13485:2016, EU MDR, GMP etc)....
Demographic Data for Memphis, TN
Moving to Memphis, TN? Find some basic demographic data about Memphis, TN below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Memphis, TN
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Memphis, TN 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
- Validation
- Medical Device Sales
- Microsoft Visio
- Legal Research & Writing
- Corrective Actions & Preventive Actions
- FDA Regulations
- Resolution
- Root Cause Analysis
- Microsoft SharePoint
- Standard Operating Procedures
- Continuous Improvement
- Product Development
- Systems Applications & Products
- Reimbursement
- Risk Management
- Engineering
- Implementation
- Written Communication
- Military Background
- Analytical Skills
- Auditing
- Microsoft Outlook
- Documentation
- Verbal Communication
- Collaboration
- Interpersonal Skills
- Investigation
- Reporting
- Policy Development
- Education Experience
- Microsoft PowerPoint
- Filing
- Bachelor's Degree
- Regulations
- Project Management
- Time Management
- Microsoft Office
- Microsoft Excel
- Sales
- Computer Skills
- Research Skills
- Staff Supervision
- Organization
- Problem Solving
- Scheduling
- Leadership
- Communication Skills
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