Manager, Regulatory Affairs CMC

What you’d do

Support preparation and submission of CMC regulatory filings including INDs, CTAs, BLAs, MAAs, supplements and variations, covering lentiviral vector manufacturing and lifecycle management. Hybrid role with three days onsite; office location is El Segundo, Thousand Oaks, Foster City, CA or Parsippany, NJ. Found on the employer's careers page on Oct 17, 2026. Apply through the link.

You’ll need

• Knowledge of CMC regulatory requirements and ICH guidelines
• Experience with INDs, CTAs, BLAs, MAAs submissions
• Strong written and verbal communication skills
• Attention to detail and organizational skills
• Three days onsite per week