Regulatory Affairs Specialist (FDA, DEA )
BaRupOn LLC
- Irvine, CA
- Permanent
- Full-time
- Prepare and manage FDA submissions (e.g., drug listings, establishment registrations, 503A/503B updates)
- Oversee and renew DEA registrations, inventory records, and security documentation
- Maintain state pharmacy, medical device, and wholesale distribution licenses
- Track regulatory changes affecting compounding, controlled substances, and labeling requirements
- Support internal audits, site inspections, and responses to 483s or warning letters
- Coordinate with Quality Assurance on SOP compliance, change controls, and deviation reports
- Serve as point of contact with federal and state regulatory agencies
- Document and file compliance records and ensure timely reporting
- Associate degree in Life Sciences, Regulatory Affairs, or related field (Bachelor's preferred)
- 2–4 years of regulatory or compliance experience in pharmaceuticals, biotech, or medical devices
- Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements
- Strong writing, documentation, and organizational skills
- Familiarity with electronic submission systems, labeling requirements, and drug master files
- Experience in sterile or non-sterile compounding (503A or 503B environments)
- Knowledge of NABP license portals, MedWatch reporting, or REMS programs
- Regulatory Affairs Certification (RAC) or DEA compliance training (preferred)
- Experience responding to FDA inspections, audits, or state pharmacy board requests
- Health, dental, and vision insurance
- 401(k) with employer match
- Paid time off and holidays
- Regulatory training and continuing education support
- Advancement opportunities into QA/RA leadership roles