Director of Regulatory Affairs Jobs in El Segundo, CA
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
- Dendreon Pharmaceuticals LLC
- Seal Beach, CA (21 miles from El Segundo, CA)
- 14 hours ago
- Seal Beach, CA (21 miles from El Segundo, CA)
- 14 hours ago
Job Summary: The Associate Director of Regulatory Affairs develops and executes global regulatory strategies to support product development, lifecycle management, and commercialization objectives....
In PersonDirector of Regulatory Affairs Radiant is seeking a highly engaging and effective leader for our regulatory and licensing team....
In Person- ABODE COMMUNITIES
- Los Angeles, CA (9 miles from El Segundo, CA)
- 4 days ago
- Los Angeles, CA (9 miles from El Segundo, CA)
- 4 days ago
Regulatory Affairs Manager ABODE COMMUNITIES - 3.2 Los Angeles, CA Job Details Full-time $90,000 - $103,000 a year 16 hours ago Qualifications Stakeholder relationship building Full Job...
In PersonDirector, Regulatory Affairs CMC
- Kite Pharma
- Santa Monica, CA (8 miles from El Segundo, CA)
- 6 days ago
- Santa Monica, CA (8 miles from El Segundo, CA)
- 6 days ago
As a Director, Global Regulatory Affairs CMC, at Gilead you will...be responsible for providing global regulatory CMC leadership and strategy across the development, lifecycle management, and commercialization...
In PersonSr Director, Regulatory Affairs CMC
- Kite Pharma
- Santa Monica, CA (8 miles from El Segundo, CA)
- 30+ days ago
- Santa Monica, CA (8 miles from El Segundo, CA)
- 30+ days ago
Were here for one reason and one reason only to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. Weve made incredible...
In PersonExecutive Director, Regulatory Affairs
- Arrowhead Pharmaceuticals, Inc.
- Pasadena, CA (22 miles from El Segundo, CA)
- 30+ days ago
- Pasadena, CA (22 miles from El Segundo, CA)
- 30+ days ago
Executive Director, Regulatory Affairs, will be the leader of the Clinical Regulatory sub-team and will have responsibility for Clinical Regulatory submissions in the US and ex-US across the entire...
In PersonDemographic Data for El Segundo, CA
Moving to El Segundo, CA? Find some basic demographic data about El Segundo, CA below.
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Salary for Director of Regulatory Affairs Jobs in El Segundo, CA
Required or preferred licenses and certifications for Director of Regulatory Affairs positions.
Highest Education Level
Director of Regulatory Affairss in El Segundo, CA 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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