Regulatory Affairs Specialist Jobs in Salisbury, MA
- Sig Sauer Inc.
- Newington, NH (15 miles from Salisbury, MA)
- 2 days ago
- Newington, NH (15 miles from Salisbury, MA)
- 2 days ago
Trade Compliance Analyst II Hybrid SIG SAUER, Inc. is a leading provider and manufacturer of firearms, electro-optics, ammunition, airguns, suppressors, remote controlled weapons stations, and...
In PersonSpecialist, Regulatory Affairs
- TransMedics Group, Inc.
- Andover, MA (20 miles from Salisbury, MA)
- 45+ days ago
- Andover, MA (20 miles from Salisbury, MA)
- 45+ days ago
ESSENTIAL TASK AND DUTIES INCLUDE: Prepare and maintain regulatory submissions and registrations of complex Class III devices in the US and in international markets Maintain documentation and perform...
In PersonRegulatory Affairs Specialist, III
- Inogen, Inc
- Beverly, MA (19 miles from Salisbury, MA)
- 60+ days ago
- Beverly, MA (19 miles from Salisbury, MA)
- 60+ days ago
The role includes obtaining and maintaining regulatory approvals, supporting quality management system (QMS) objectives, and ensuring adherence to applicable regulatory standards....
In PersonRegulatory Affairs Specialist (Austin, TX)
- Smith & Nephew
- Andover, MA (20 miles from Salisbury, MA)
- 90+ days ago
- Andover, MA (20 miles from Salisbury, MA)
- 90+ days ago
Knowledge of regulatory compliance requirements (e.g. 21 CFR 820, ISO13485:2016, EU MDR, GMP etc)....
HybridDemographic Data for Salisbury, MA
Moving to Salisbury, MA? Find some basic demographic data about Salisbury, MA below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Salisbury, MA
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Salisbury, MA 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
- Audit Support
- 21 CFR 820
- ISO 13485
- Quality Systems
- Internal Control
- Medical Device Sales
- Validation
- Microsoft Visio
- FDA Regulations
- Corrective Actions & Preventive Actions
- Resolution
- Root Cause Analysis
- Microsoft SharePoint
- Continuous Improvement
- Standard Operating Procedures
- Product Development
- Reimbursement
- Risk Management
- Engineering
- Implementation
- Military Background
- Analytical Skills
- Written Communication
- Auditing
- Process Improvement
- Microsoft Outlook
- Documentation
- Verbal Communication
- Data Analysis
- Collaboration
- Investigation
- Reporting
- Regulations
- Bachelor's Degree
- Policy Development
- Microsoft PowerPoint
- Filing
- Education Experience
- Research Skills
- Project Management
- Time Management
- Microsoft Office
- Sales
- Staff Supervision
- Microsoft Excel
- Problem Solving
- Scheduling
- Leadership
- Communication Skills
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