Regulatory Affairs Specialist Jobs in Suffern, NY
The Director of Regulatory Affairs in the quality control industry plays an essential role in ensuring that the company's products meet all regulatory standards and compliance requirements. This individual oversees the development and implementation of regulatory strategies for new and existing products, supervises the preparation of regulatory submissions, and maintains communication with regulatory authorities. They also monitor changes in regulations, interpret these updates for relevant departments within the company, and implement necessary changes to maintain compliance. They are responsible for setting the company's standards for quality, safety, and efficacy.
To excel in this role, one should possess excellent analytical skills, strategic thinking, and strong leadership abilities. A deep understanding of regulatory guidelines, ability to interpret complex regulations, and excellent communication skills are essential. They should have a degree in a relevant field, along with certifications such as Regulatory Affairs Certification (RAC), Certified Quality Auditor (CQA), and Certified Quality Engineer (CQE). Prior to becoming a Director of Regulatory Affairs, individuals might have roles such as Regulatory Affairs Specialist, Regulatory Affairs Manager, or Quality Control Manager.
Lead Compliance Analyst (Broker-Dealer, Investment Advisor, Insurance Agency)
- Harrison, NY (22 miles from Suffern, NY)
- 1 day ago
- Harrison, NY (22 miles from Suffern, NY)
- 1 day ago
These are supported by Transamerica Corporate, which includes Finance, People and Places, General Counsel, Risk, Internal Audit, Strategy and Development, and Corporate Affairs, which covers Communications...
Regulatory Affairs Specialist (Wayne, NJ)
- Wayne, NJ (14 miles from Suffern, NY)
- 5 days ago
- Wayne, NJ (14 miles from Suffern, NY)
- 5 days ago
Job title: Senior Regulatory Affairs Specialist Salary: $111,925 to $150,000 Job Location: 45 Barbour Pond Drive, Wayne, NJ 07470 Education: Bachelor's degree in Engineering or a related field....
Compliance Analyst, 340B Program
- Valhalla, NY (17 miles from Suffern, NY)
- 5 days ago
- Valhalla, NY (17 miles from Suffern, NY)
- 5 days ago
Job Summary: The 340B Program Compliance Analyst is responsible for maintaining regulatory compliance within the 340B Program across all WMCHealth entities. This role ensures adherence to HRSA...
Regulatory and Compliance Specialist
- Bronx, NY (24 miles from Suffern, NY)
- 21 days ago
- Bronx, NY (24 miles from Suffern, NY)
- 21 days ago
Job Description: Regulatory and Compliance Specialist is needed to perform the following duties: oResponsible for REGULATORY COMPLIANCE leading to pharmacy management. Evaluating and ensuring...
Regulatory Affairs Specialist (Food & Beverage)
- Saddle Brook, NJ (16 miles from Suffern, NY)
- 24 days ago
- Saddle Brook, NJ (16 miles from Suffern, NY)
- 24 days ago
US FDA regulation experience and familiarity with allergen list required. USDA Labeling experience is highly desired....
- Teaneck, NJ (17 miles from Suffern, NY)
- 45+ days ago
- Teaneck, NJ (17 miles from Suffern, NY)
- 45+ days ago
Interstate Waste Services, Inc. Corporate Compliance Analyst in Teaneck , New Jersey Overview Interstate Waste Services is the most progressive and innovative provider of solid waste and recycling...
Demographic Data for Suffern, NY
Moving to Suffern, NY? Find some basic demographic data about Suffern, NY below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Suffern, NY
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Suffern, NY offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Regulatory Affairs Specialist position
- Finance
- Medicaid
- Flexibility
- Call Center Experience
- Medicare
- Internal Control
- Management Reporting
- Fraud Investigation
- Reimbursement
- Institutional Review Board
- Internal Audits
- 21 CFR 820
- ICH Guidelines
- ISO 13485
- Validation
- Medical Device Sales
- Business Processes
- FDA Regulations
- Microsoft Visio
- Resolution
- Standard Operating Procedures
- Product Development
- Engineering
- Risk Management
- Strategy Development
- Implementation
- Auditing
- Investigation
- Written Communication
- Verbal Communication
- Documentation
- Collaboration
- Data Analysis
- Interpersonal Skills
- Reporting
- Education Experience
- Bachelor's Degree
- Filing
- Regulations
- Microsoft PowerPoint
- Sales
- Policy Development
- Project Management
- Problem Solving
- Microsoft Office
- Microsoft Excel
- Research Skills
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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