Regulatory Affairs Specialist Jobs in Newbury, MA
- Sig Sauer Inc.
- Newington, NH (21 miles from Newbury, MA)
- 16 hours ago
- Newington, NH (21 miles from Newbury, MA)
- 16 hours 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 (17 miles from Newbury, MA)
- 30+ days ago
- Andover, MA (17 miles from Newbury, MA)
- 30+ 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 (12 miles from Newbury, MA)
- 60+ days ago
- Beverly, MA (12 miles from Newbury, 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 (17 miles from Newbury, MA)
- 90+ days ago
- Andover, MA (17 miles from Newbury, MA)
- 90+ days ago
Knowledge of regulatory compliance requirements (e.g. 21 CFR 820, ISO13485:2016, EU MDR, GMP etc)....
HybridDemographic Data for Newbury, MA
Moving to Newbury, MA? Find some basic demographic data about Newbury, MA below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Newbury, MA
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Newbury, 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
- Military Background
- Written Communication
- Implementation
- Analytical Skills
- Auditing
- Process Improvement
- Microsoft Outlook
- Documentation
- Verbal Communication
- Data Analysis
- Collaboration
- Investigation
- Reporting
- Regulations
- Bachelor's Degree
- Policy Development
- Microsoft PowerPoint
- Filing
- Education Experience
- Project Management
- Time Management
- Research Skills
- Microsoft Office
- Sales
- Staff Supervision
- Microsoft Excel
- Customer Service
- Problem Solving
- Scheduling
- Leadership
- Communication Skills
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