Regulatory Affairs Specialist Jobs in Weldon Spring, MO
- eTeam
- Chesterfield, MO (5 miles from Weldon Spring, MO)
- 9 days ago
- Chesterfield, MO (5 miles from Weldon Spring, MO)
- 9 days ago
Title: US- Regulatory Affairs Specialist (Entry) Location: Chesterfield, MO 63017 Duration: 06 Months role with possibility of extension The expectation is 3 days per week at our Chesterfield, MO site...
In PersonUS Regulatory Affairs Specialist Entry
- Adecco US, Inc.
- Chesterfield, MO (5 miles from Weldon Spring, MO)
- 15 days ago
- Chesterfield, MO (5 miles from Weldon Spring, MO)
- 15 days ago
Opening for Regulator Affairs in Chesterfield MO. Apply Today Hybrid (3 days a week onsite) Mon-Fri 8am-5pm The anticipated wage for this position is $39.12. Hourly wage may depend upon...
In Person- Entegee
- Maryland Heights, MO (11 miles from Weldon Spring, MO)
- 18 days ago
- Maryland Heights, MO (11 miles from Weldon Spring, MO)
- 18 days ago
Summary: Seeking a Regulatory Affairs Specialist to support international drug product applications and manage regulatory activities for market expansion....
In Person- Randstad
- Chesterfield, MO (5 miles from Weldon Spring, MO)
- 19 days ago
- Chesterfield, MO (5 miles from Weldon Spring, MO)
- 19 days ago
We are seeking a highly organized and detail-oriented Regulatory Affairs Specialist to support our team in managing state regulatory activities for crop protection products....
HybridDemographic Data for Weldon Spring, MO
Moving to Weldon Spring, MO? Find some basic demographic data about Weldon Spring, MO below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Weldon Spring, MO
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Weldon Spring, MO offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Regulatory Affairs Specialist position
- 21 CFR 820
- Internal Audits
- Institutional Review Board
- Good Clinical Practice
- ISO 13485
- Change Control
- Document Management
- Medical Device Sales
- Corrective Actions & Preventive Actions
- FDA Regulations
- Resolution
- Standard Operating Procedures
- Product Development
- Continuous Improvement
- Microsoft SharePoint
- Technical Writing
- Strategy Development
- Reimbursement
- Engineering
- Risk Management
- Analytical Skills
- Auditing
- Implementation
- Written Communication
- Military Background
- Collaboration
- Process Improvement
- Documentation
- Verbal Communication
- Data Analysis
- Investigation
- Reporting
- Education Experience
- Bachelor's Degree
- Policy Development
- Microsoft PowerPoint
- Filing
- Project Management
- Research Skills
- Regulations
- Microsoft Office
- Time Management
- Staff Supervision
- Microsoft Excel
- Problem Solving
- Teamwork
- Scheduling
- Leadership
- Communication Skills
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