Regulatory Affairs Specialist Jobs in Lakehurst, NJ
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.
- Trenton, NJ (22 miles from Lakehurst, NJ)
- 6 days ago
- Trenton, NJ (22 miles from Lakehurst, NJ)
- 6 days ago
Job Order Number: DE9405993 Job Title: Trade Compliance Analyst Company: Otsuka America Pharmaceutical Inc. Location: Trenton, NJ Salary: Education: Less Than High School Experience: None Hours:...
Food Safety & Regulatory Compliance Specialist
- Cranbury, NJ (22 miles from Lakehurst, NJ)
- 7 days ago
- Cranbury, NJ (22 miles from Lakehurst, NJ)
- 7 days ago
Support the maintenance and review of key food safety and quality systems, including pest control, sanitation, GMP, and internal auditing....
Marketing and Product Compliance Analyst
- Trenton, NJ (22 miles from Lakehurst, NJ)
- 9 days ago
- Trenton, NJ (22 miles from Lakehurst, NJ)
- 9 days ago
Job Order Number: DE9400799 Job Title: Marketing and Product Compliance Analyst Company: Zoom Location: Trenton, NJ Salary: Education: Less Than High School Experience: None Hours: Duration: Full...
Compliance Analyst Sr--Medical Pharmacy Specialty/Medicare Part B- REMOTE
- Trenton, NJ (22 miles from Lakehurst, NJ)
- 14 days ago
- Trenton, NJ (22 miles from Lakehurst, NJ)
- 14 days ago
Our work matters. We help people get the medicine they need to feel better and live well. We do not lose sight of that. It fuels our passion and drives every decision we make. Job Posting Title...
Remote Work- Trenton, NJ (22 miles from Lakehurst, NJ)
- 18 days ago
- Trenton, NJ (22 miles from Lakehurst, NJ)
- 18 days ago
Responsible for assisting the Regulatory Team with the processes of maintenance and registration of new products and state wholesaler licenses as required from the FDA (Food and Drug...
Renewable Natural Gas Regulatory Compliance Analyst
- Jackson, NJ (7 miles from Lakehurst, NJ)
- 25 days ago
- Jackson, NJ (7 miles from Lakehurst, NJ)
- 25 days ago
Renewable Natural Gas Regulatory Compliance Analyst Suburban Propane Location Jackson Twp Posted date 9 hours ago Minimum level N/A Job type Full-time Job category Other Over When you join...
Demographic Data for Lakehurst, NJ
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Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Lakehurst, NJ
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Lakehurst, NJ offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Regulatory Affairs Specialist position
- Analytical Skills
- Filing
- Financial Services
- Mortgage Processing
- Reimbursement
- Juris Doctor
- Institutional Review Board
- Internal Audits
- Quality Systems
- Quality Management Systems
- 21 CFR 820
- ICH Guidelines
- Corrective Actions & Preventive Actions
- ISO 13485
- Medical Device Sales
- Business Processes
- FDA Regulations
- Microsoft Visio
- Lean Six Sigma
- Standard Operating Procedures
- Engineering
- Product Development
- Affirmative Action
- Risk Management
- Quality Assurance
- Process Improvement
- Implementation
- Military Background
- Auditing
- High School Diploma
- Investigation
- Written Communication
- Verbal Communication
- Documentation
- Collaboration
- Reporting
- Education Experience
- Bachelor's Degree
- Regulations
- Microsoft PowerPoint
- Policy Development
- Project Management
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Time Management
- Teamwork
- Research Skills
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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