Regulatory Affairs Specialist Jobs in Marietta, PA
Specialist, Regulatory Affairs TMTT
- Edwards Lifesciences LLC
- Camp Hill, PA (21 miles from Marietta, PA)
- 3 days ago
- Camp Hill, PA (21 miles from Marietta, PA)
- 3 days ago
Track timelines and documents milestone achievements for inclusion in regulatory submissions....
In PersonSenior Specialist, Regulatory Affairs TMTT
- Edwards Lifesciences LLC
- Camp Hill, PA (21 miles from Marietta, PA)
- 22 days ago
- Camp Hill, PA (21 miles from Marietta, PA)
- 22 days ago
Track timelines and documents milestone achievements for inclusion in regulatory submissions. May interact with regulatory agencies as part of submission review and on-site audit support....
HybridCommercial Risk and Compliance Analyst
- Fulton Financial
- Lancaster, PA (13 miles from Marietta, PA)
- 30+ days ago
- Lancaster, PA (13 miles from Marietta, PA)
- 30+ days ago
Value Proposition Our values define us and our culture inspires us to change lives for the better. Our employees are the heart and soul of our company, and every success we experience begins with...
HybridInformation Security Governance Risk & Compliance Analyst
- PSECU
- Harrisburg, PA (20 miles from Marietta, PA)
- 90+ days ago
- Harrisburg, PA (20 miles from Marietta, PA)
- 90+ days ago
Internal Audit Coordination: Collect evidence for internal and external audits. Research and respond to internal and external audit finding Other duties as assigned....
In PersonDemographic Data for Marietta, PA
Moving to Marietta, PA? Find some basic demographic data about Marietta, PA below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Marietta, PA
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Marietta, PA 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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