Director of Regulatory Affairs Jobs in New Jersey
Associate Director, Regulatory Affairs
- Franklin Lakes, NJ
- 10 hours ago
- Franklin Lakes, NJ
- 10 hours ago
Job Description Summary As Associate Director, Regulatory Affairs, you will be responsible for leading RA team members involved in device project activities and new product development in Advanced Drug...
Executive Director Regulatory Affairs Job ID: 7663 Job Title: Executive Director Regulatory Affairs Location: New Jersey, NJ My client is a commercial-stage pharmaceutical company with a strong portfolio...
Associate Director, Regulatory Affairs - Labeling Management
- Rahway, NJ
- 5 days ago
- Rahway, NJ
- 5 days ago
Regulations, Management Process, Pharmacovigilance, Policy Implementation, Regulatory Affairs Compliance, Regulatory Compliance, Regulatory Labeling, Regulatory Operations, Regulatory Submissions,...
Associate Director/Director, Regulatory Affairs -GDP Contractor
- Florham Park, NJ
- 6 days ago
- Florham Park, NJ
- 6 days ago
Performance metrics will include completion of regulatory submissions, adherence to timelines, and the quality of submissions The Executive Director, Regulatory Affairs will review and approve completed...
Manager, Regulatory Affairs Zydus Pharmaceuticals USA Inc. United States, Jersey, Pennington Jul 23, 2025 Manager, Regulatory Affairs - Pharmaceuticals Co. (Pennington, NJ) seeks Manager,...
Director, Regulatory Affairs Location : Morristown, NJ area (2 days per week onsite). Compensation : Base salary up to $220k, Plus Bonus, Plus LTI....
Associate Principal Scientist (Associate Director) Regulatory Affairs
- Rahway, NJ
- 12 days ago
- Rahway, NJ
- 12 days ago
Job Description GRACS CMC Associate Principal Scientist, CMC, R4 Pharm Pre-approval Reporting to the Sr Director/Director/Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical...
Associate Director, Regulatory Affairs Advertising & Promotion Compliance
- Princeton, NJ
- 15 days ago
- Princeton, NJ
- 15 days ago
Summary: The Associate Director, Regulatory Affairs, Advertising and Promotion Compliance will independently review, approve, and monitor product advertising and promotional labeling material for an...
Your Dreams, Our Future. Join the dynamic and diverse team at Shiseido Americas, a subsidiary of the world-renowned Shiseido Company Limited. Be a part of a portfolio of prestige beauty brands...
General Information Country United States City Pennsville, New Jersey Functional Area Research & Development Job Group Regulatory Affairs Employment Type Permanent Contract Working time Full-time...
Executive Director, Regulatory Affairs Strategist
- Bridgewater, NJ
- 30+ days ago
- Bridgewater, NJ
- 30+ days ago
Overview The Executive Director, Regulatory Affairs Strategist provides regulatory expertise and guidance on procedural and documentation requirements to Global Regulatory Teams (GRTs) and cross-functional...
Director, US Regulatory Affairs Join Minaris Advanced Therapies, a global leader in cell and gene therapy development, manufacturing, and testing!...
regulations, including 21 CFR 1271 and 21 CFR 312 **Job Location** This role is located onsite in our Eden Prairie, MN (Miromatrix) location with the option for a remote candidate with monthly travel...
HR Control Manager - Regulatory Affairs - Vice President
- Jersey City, NJ
- 45+ days ago
- Jersey City, NJ
- 45+ days ago
JobID: 210574564 Category: Control Officers JobSchedule: Full time Posted Date: 2025-06-18T04:00:00+00:00 JobShift: Day Base Pay/Salary: Jersey City,NJ $118,750.00-$190,000.00 Join our HR Control...
Description Manager, Regulatory Affairs (Hybrid) About Us: Join Hartz, where our love for pets drives everything we do. With over 95 years of commitment to pet care excellence, we are a trusted...
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Director of Regulatory Affairss in New Jersey offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Director of Regulatory Affairs position
- Gene Therapy
- Supplier Auditing
- Medical Affairs
- Drug Discovery
- 21 CFR 820
- Internal Audits
- Pharmacovigilance
- ICH Guidelines
- Drug Development
- Immunology
- Change Control
- GxP
- Quality Systems
- Biochemistry
- ISO 13485
- Biotechnology
- Quality Management Systems
- Biology
- Product Launch
- Medical Device Sales
- Document Management
- Clinical Trials
- Research and Development
- Clinical Research
- FDA Regulations
- Standard Operating Procedures
- Product Development
- Masters In Education
- Engineering
- Strategy Development
- Implementation
- Written Communication
- Military Background
- Auditing
- Education Experience
- Collaboration
- Documentation
- Mentoring
- Interpersonal Skills
- Reporting
- Employee Development
- Quality Assurance
- Coaching
- Filing
- Policy Development
- Problem Solving
- Bachelor's Degree
- Regulations
- Project Management
- Microsoft Excel
- Time Management
- Research Skills
- Teamwork
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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