FDA Submissions Specialist

The Opportunity We are seeking a seasoned FDA Submissions Specialist who brings deep, hands-on expertise in navigating the full spectrum of FDA submission processes. This is not an advisory role — we need someone who has personally led and authored regulatory submissions, understands the intricacies of Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and Good Clinical Practice (GCP), and can serve as a strategic regulatory partner across the organization. You will take direct ownership of our submission pipeline, drive regulatory strategy from early development through approval, and be the internal authority on FDA requirements, pathways, and evolving guidance. Non-Negotiable Requirement Candidates must have direct, hands-on experience preparing and submitting at least one of the following to the

FDA:

510(k), IND, BLA, NDA or PMA. Advisory or supporting roles do not meet this requirement — we are looking for individuals who served as core contributors to the submission itself. What You'll Do Lead the end-to-end preparation, assembly, and submission of FDA applications — including 510(k)s, INDs, BLAs, and PMAs — from initial planning through agency receipt, ensuring completeness, accuracy, and strategic framing at every step. Manage the full lifecycle of active submissions, including amendments, supplements, annual reports, and responses to FDA information requests or deficiency letters. Author and review responses to FDA information requests, deficiency letters, Complete Response Letters (CRLs), and Refuse-to-File (RTF) notifications with clarity and technical precision. Serve as the primary point of contact for FDA interactions — preparing meeting requests, briefing documents, and written responses, and representing the company during agency communications. Develop and own regulatory strategy for pipeline programs, assessing submission pathways, identifying risks early, and advising leadership on optimal routes to approval. Advise leadership and cross-functional stakeholders on regulatory requirements, timelines, and strategic options to support program decisions. Ensure ongoing inspection readiness by maintaining robust regulatory compliance across all processes, documentation, and activities per 21 CFR Parts 11, 50, 54, 56, 58, 210/211, 312, 314, 600-series, 820, and applicable ICH guidelines (E6, Q8-Q10). Support internal audits, CAPA development, and gap assessments aligned with GLP, GMP, and GCP standards. Collaborate cross-functionally with Clinical Operations, Medical Affairs, R&D, and Quality to align regulatory requirements with program timelines and deliverables. Provide regulatory support for Chemistry, Manufacturing, and Controls (CMC) sections of INDs, BLAs, NDAs, and supplements, including review of drug substance and drug product specifications, stability data, and manufacturing process descriptions. Support regulatory strategy for CMC development milestones, including IND- enabling studies, Phase 2/3 manufacturing scale-up, and BLA/NDA readiness assessments aligned with ICH Q8, Q9, Q10, and Q11 guidelines. Provide regulatory training and guidance to internal teams on submission requirements, compliance obligations, and agency expectations. What You'll Bring Education & Experience Bachelor's degree in a scientific or engineering discipline; advanced degree (M.S., Ph.D., Pharm.

D., RAC) strongly preferred. 5+ years of FDA regulatory affairs experience in biotech, pharma, or medical devices, with verifiable, hands-on submission authorship. Direct experience with one or more submission types: 510(k), IND, BLA, or PMA — from drafting through submission and agency follow-up. Experience with both drug/biologic and device regulatory pathways is a strong differentiator. Skills and Attributes Deep command of 21 CFR Parts 50, 54, 56, 58, 210/211, 312, 314, 600-series, and 820, as well as ICH guidelines (E6 GCP, Q8-Q10 pharmaceutical development, and M4 CTD format). Familiarity with eCTD structure and electronic submission requirements via the FDA Electronic Submissions Gateway (ESG). Understanding of nonclinical study designs (GLP toxicology, pharmacology) andtheir regulatory significance for

IND/NDA/BLA

filings. Ability to clearly communicate complex regulatory requirements to both technical and non-technical stakeholders, including senior leadership. Highly organized and detail-oriented, with the ability to manage multiple submissions and priorities simultaneously in a fast-paced environment. Hybrid role but MUST be based out of Los Angeles, CA.

Benefits:

Competitive salary: $27-45 an hour Comprehensive health benefits package including medical, dental, and vision insurance.

Job Type:

Full-time Pay:

$30.00 - $45.00 per hour

Benefits:

Dental insurance Health insurance Paid time off Vision insurance

Work Location:

Hybrid remote in Los Angeles, CA 90066