Full-time
Regulatory Affairs Manager
Competitive
Greater Los Angeles, CaliforniaScience & PharmaceuticalPosted 16d ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
16 days ago
Job description
Responsibilities
Assist in the preparation, review, and submission of INDs, BLAs, NDAs, amendments, and other regulatory filings
Monitor regulatory changes and communicate updates to relevant teams to ensure ongoing compliance
Coordinate with internal departments and external partners to gather necessary documentation for regulatory submissions
Maintain accurate records of regulatory correspondence and submissions
Support audits and inspections by regulatory authorities
Preferred
Bachelor's degree in life sciences, pharmacy, or a related field
advanced degree
Benefits
Hybrid work arrangement in Los Angeles
Immix Biopharma, Inc.
Los Angeles, California, USA
http://www.immixbio.com
Public Company
Total Funding
$399.1M
Key Investors
GOOSE Capital
Mesa Verde Venture Partners
2026-09-29
Post Ipo Equity· $125M
2026-05-21
Post Ipo Equity· $150M
2025-12-07
Post Ipo Equity· $100M
Leadership Team
Michael Grabow
Chief Commercial Officer (CCO)
Recent News
StreetInsider.com
Immix Biopharma prices $125M common stock offering at $11 per share
2026-10-03
MarketScreener
Immix Biopharma Closes $125 Million Stock Offering
2026-10-01
BioSpace
Immix Biopharma Announces Closing of $125 Million Underwritten Offering of Common Stock
Company data provided by
AI Tools
Qualifications
The ideal candidate will demonstrate strong attention to detail, analytical skills, and knowledge of FDA/EMA/HealthCanada/MHRA requirements for investigational products
3-5 years of experience in regulatory affairs within the biopharmaceutical industry
Familiarity with FDA/EMA/HealthCanada/MHRA regulations, clinical trial processes, and regulatory submission requirements
Strong written and verbal communication skills
Excellent organizational and project management abilities
Familiarity with eCTD submissions and regulatory software tools
Ability to work effectively in a collaborative, fast-paced environment
Attention to detail and analytical problem-solving skills
Bachelor's degree in life sciences, pharmacy, or a related field
Advanced degree
3-5 years of experience in regulatory affairs within the biopharmaceutical industry.
Required skills
Regulatory Affairs, FDA/EMA/Health Canada/MHRA Regulations, Clinical Trial Processes, Regulatory Submissions, eCTD
Preferred skills
Project Management, Written and Verbal Communication
Experience
3-5 years
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