Director of Regulatory Affairs Jobs in Tarrytown, 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.
Associate Director, Regulatory Affairs
- Recursion Pharmaceuticals
- New York, NY (24 miles from Tarrytown, NY)
- 20 days ago
- New York, NY (24 miles from Tarrytown, NY)
- 20 days ago
We are seeking an Associate Director of Regulatory Affairs who will play a critical role in supporting global regulatory strategy, overseeing processes, and identifying and managing regulatory risks...
Remote- Bausch + Lomb
- Ridgewood, NJ (15 miles from Tarrytown, NY)
- 23 days ago
- Ridgewood, NJ (15 miles from Tarrytown, NY)
- 23 days ago
Job Order Number: DF0735055 Job Title: Director, Regulatory Affairs Company: Bausch + Lomb Location: Ridgewood, NJ Salary: Education: Information Not Provided Experience: Information Not Provided Hours...
In PersonManager/Senior Manager, Regulatory Affairs Operations
- Axsome Therapeutics, Inc.
- New York, NY (24 miles from Tarrytown, NY)
- 30+ days ago
- New York, NY (24 miles from Tarrytown, NY)
- 30+ days ago
This role reports to the Executive Director, Regulatory Affairs. This role is based at Axsome's HQ in New York City with an on-site requirement of at least three days per week....
RemoteRegulatory Affairs Director - Hybrid
- CareSource
- Bronx, NY (18 miles from Tarrytown, NY)
- 30+ days ago
- Bronx, NY (18 miles from Tarrytown, NY)
- 30+ days ago
Job Summary: The Regulatory Affairs Director is responsible for leading activities of the Regulatory Affairs Department, including contracts, compliance, surveys, audits, investigations,...
HybridDirector, Regulatory Affairs Strategy - Oncology
- Regeneron Pharmaceuticals, Inc.
- Sleepy Hollow, NY
- 45+ days ago
- Sleepy Hollow, NY
- 45+ days ago
Director, Regulatory Affairs Strategy - Oncology Employer Regeneron Pharmaceuticals, Inc....
In PersonAssociate Director/Director, Regulatory Affairs
- Axsome Therapeutics, Inc.
- New York, NY (24 miles from Tarrytown, NY)
- 45+ days ago
- New York, NY (24 miles from Tarrytown, NY)
- 45+ days ago
About This Role Axsome Therapeutics is seeking an Associate Director/Director, Regulatory Affairs....
RemoteDemographic Data for Tarrytown, NY
Moving to Tarrytown, NY? Find some basic demographic data about Tarrytown, NY below.
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Salary for Director of Regulatory Affairs Jobs in Tarrytown, NY
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Director of Regulatory Affairss in Tarrytown, NY offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Director of Regulatory Affairs position
- Clinical Research
- Biology
- Virology
- Immunology
- Oncology
- Medical Writing
- Drug Development
- Neuroscience
- Biostatistics
- Clinical Trials
- Drug Discovery
- Toxicology
- Biotechnology
- Pharmacovigilance
- Medical Affairs
- Gene Therapy
- ICH GCP
- Quality Management Systems
- 21 CFR 820
- ICH Guidelines
- Good Laboratory Practice
- ISO 13485
- Microbiology
- Document Management
- Research and Development
- Medical Device Sales
- FDA Regulations
- Standard Operating Procedures
- Product Development
- Analytical Skills
- Quality Assurance
- Engineering
- Strategy Development
- Auditing
- Process Improvement
- Documentation
- Coaching
- Mentoring
- Interpersonal Skills
- Writing Skills
- Implementation
- Verbal Communication
- Reporting
- Education Experience
- Collaboration
- Bachelor's Degree
- Regulations
- Research Skills
- Microsoft Office
- Project Management
- Problem Solving
- Staff Supervision
- Scheduling
- Teamwork
- Leadership
- Communication Skills
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