Regulatory Affairs Specialist Jobs in Green Valley, 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.
Senior Regulatory Affairs Specialist
- Santa Clarita, CA (10 miles from Green Valley, CA)
- 6 days ago
- Santa Clarita, CA (10 miles from Green Valley, CA)
- 6 days ago
The Senior Regulatory Affairs Specialist will be a part of the Neuromodulation Regulatory Affairs team....
- Santa Clarita, CA (10 miles from Green Valley, CA)
- 14 days ago
- Santa Clarita, CA (10 miles from Green Valley, CA)
- 14 days ago
Company: Kelly Services Location: Santa Clarita, CA Career Level: Associate Industries: Recruitment Agency, Staffing, Job Board Description Regulatory Affairs Specialist - Valencia, CA Kelly Science...
- Valencia, CA (10 miles from Green Valley, CA)
- 16 days ago
- Valencia, CA (10 miles from Green Valley, CA)
- 16 days ago
Regulatory Affairs Specialist Valencia, CA Kelly Science & Clinical is seeking a Regulatory Specialist for a temporary, long-term position (approx. 1 year) at a biotech company in Valencia, CA, with...
Principal Quality Compliance Analyst
- Valencia, CA (10 miles from Green Valley, CA)
- 21 days ago
- Valencia, CA (10 miles from Green Valley, CA)
- 21 days ago
Bridge the gap on the Global vs local Quality System documentation by proactive review and assessment....
Regulatory Affairs Specialist II Cardiac Rhythm Management (on-site)
- Sylmar, CA (14 miles from Green Valley, CA)
- 30+ days ago
- Sylmar, CA (14 miles from Green Valley, CA)
- 30+ days ago
The Opportunity We are presently hiring for a Regulatory Affairs Specialist II to work on-site at our Cardiac Rhythm Management (CRM) location in Sylmar, CA....
Senior Regulatory Affairs Specialist Cardiac Rhythm Management (on-site)
- Sylmar, CA (14 miles from Green Valley, CA)
- 90+ days ago
- Sylmar, CA (14 miles from Green Valley, CA)
- 90+ days ago
The Opportunity Our location in Sylmar, CA currently has an on-site opportunity for a Senior Regulatory Affairs Specialist with our Cardiac Rhythm Management division....
Demographic Data for Green Valley, CA
Moving to Green Valley, CA? Find some basic demographic data about Green Valley, CA below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Green Valley, CA
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Green Valley, CA offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Regulatory Affairs Specialist position
- Filing
- Financial Services
- Mortgage Processing
- Reimbursement
- Juris Doctor
- Internal Audits
- Quality Systems
- 21 CFR 820
- ISO 9001
- ICH Guidelines
- Corrective Actions & Preventive Actions
- ISO 13485
- ISO 14001
- Quality Management
- Process Controls
- Medical Device Sales
- Business Processes
- FDA Regulations
- Microsoft Visio
- Standard Operating Procedures
- Engineering
- Product Development
- Affirmative Action
- Risk Management
- Quality Assurance
- Process Improvement
- Implementation
- Military Background
- Auditing
- Investigation
- Written Communication
- Verbal Communication
- Documentation
- Collaboration
- Interpersonal Skills
- 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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