Email Alert for
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.
Confidential
Los Angeles, CA, United States
Senior Director, Regulatory Affairs About the Company International labelling organization based in Los Angeles Industry Retail Type Privately Held About the Role The Senior Director, Regulatory Affairs will be responsible for developing and managing labeling for products worldwide as well as overseeing the strategic regulatory leveling HA interact
Job Source: ConfidentialMeet
, CA, United States
Senior Director, Regulatory Affairs (Generalist) Remote Position for West Coast-based candidates, frequent travel to Bay Area required Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs an
Job Source: MeetConfidential
Los Angeles, CA, United States
Senior Director, Regulatory Affairs About the Company International labelling organization based in Los Angeles Industry Retail Type Privately Held About the Role The Senior Director, Regulatory Affairs will be responsible for developing and managing labeling for products worldwide as well as overseeing the strategic regulatory leveling HA intera
Job Source: ConfidentialMeet
, CA, United States
Meets clinical-stage biopharmaceutical client based in the Bay Area is seeking a highly motivated individual to join their growing regulatory affairs group. The Associate Director / Director, Regulatory Affairs will work closely with the Regulatory Affairs team and other departments to develop and implement regulatory strategies for the company's r
Job Source: MeetBioTalent
, CA, United States
This individual will join our client's regulatory team and collaborate with other departments like R&D, Manufacturing, Quality Assurance, and Commercial. Here's what you'll be responsible for: Preparing Regulatory Submissions: You'll draft submissions for international markets and the FDA, including Technical Documents, Files, Device Applications
Job Source: BioTalentMeet
, CA, United States
Senior Director/Executive Director, Regulatory Affairs *Onsite 2-3 days weekly in South San Francisco, CA* Meet has partnered with a pre-IPO biotech that is looking for a Head of Regulatory Affairs to join their team. This will be the first full-time RA hire for the organization and you will be reporting directly into the CEO. Our client is based
Job Source: MeetAbbott Laboratories company
Los Angeles, CA, United States
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
Job Source: Abbott Laboratories companyAmgen Inc. (IR)
Los Angeles, CA, United States
Executive Director, Regulatory Affairs page is loaded Executive Director, Regulatory Affairs Apply remote type Remote locations US - California - Los Angeles time type Full time posted on Posted 2 Days Ago job requisition id R-190059 Career Category Regulatory Job Description HOW MIGHT YOU DEFY IMA
Job Source: Amgen Inc. (IR), CA, United States
Senior Director, Regulatory Affairs (Generalist)
Remote Position for West Coast-based candidates, frequent travel to Bay Area required
Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions. Our client recently reported positive P3 data for their lead drug candidate and is in the process of filing an NDA this year.
Key Responsibilities:
Carry out Reg Strategy and Reg CMC functions to support major Regulatory submissions
Serve as a cross-functional leader within the organization to facilitate prompt and accurate regulatory documentation
Key Qualifications/Requirements
12+ years of Regulatory Affairs (mix of Clinical Reg and Reg CMC highly preferred)
NDA/late stage experience highly preferred
Non-oncology experience required, rare disease preferred
Small molecule development experience required
Startup experience highly preferred
Please feel free to reach out directly to Ryan Moran to learn more:
#J-18808-Ljbffr
Email Alert for Senior Director, Regulatory Affairs jobs in , CA, United States
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.