CMC Regulatory Lead at Retro

Redwood City, California, United States -

Full Time

Start Date

Immediate

Expiry Date

22 May, 26

Salary

240000.0

Posted On

21 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

CMC Regulatory Strategy, Cell Therapy, Small Molecules, IND Submissions, CTA Submissions, Marketing Applications, Health Authority Interactions, Regulatory CMC, Process Development, Analytical Development, CDMO Oversight, Risk Mitigation, Cross-functional Leadership, Operational Discipline, Regulatory CMC Planning, Technical Translation

Industry

Biotechnology Research

Description

Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan. We’re hiring an experienced CMC Regulatory Lead to own the strategy and operations for our Chemistry, Manufacturing, and Controls (CMC) regulatory work. As one of the earliest members of the Regulatory Affairs team, you will work across Retro’s programs and play a leading role in building out the regulatory CMC capabilities and strategies to achieve our ambitious mission and tackle aging. You will report directly to the leader of Regulatory Affairs. This position is an onsite role based in Redwood City. About you: You are a builder and doer who can set clear, global CMC regulatory strategies and roll up your sleeves to execute them at speed. You are energized by complex CMC challenges, especially in cell therapy, and you anticipate questions before they become risks. You translate technical details into clear regulatory narratives that resonate with health authorities, and you are comfortable serving as the CMC regulatory point person in high-stakes health-authority interactions. You have high-collaboration and low-ego tendencies, with the ability to align cross-functional technical teams and external partners around a shared regulatory CMC plan and clear deliverables. You bring strong operational discipline, enjoy creating structure when needed, and are mission-driven with genuine motivation to advance longevity and aging biology for the benefit of humanity. \n In this role, you will: Be accountable for the regulatory CMC activities for Retro’s programs, which include both cell therapies and small molecules. Develop the regulatory CMC strategy for each program and lead the execution of global CMC regulatory plans. Lead the preparation of the CMC dossier for INDs/CTAs and marketing applications, as well as the CMC documents for amendments, annual reports, and other CMC regulatory submissions. Act as Retro’s regulatory liaison with health authorities for CMC communications and submissions. Lead health-authority meetings with FDA and other health authorities for CMC-related topics. Lead the responses to health-authority queries and information requests related to CMC. Identify regulatory CMC risks and develop creative and innovative mitigation strategies. Partner closely with key internal functions, including Analytical Development, Process Development, Scientific Operations, and Quality. Provide regulatory CMC guidance and oversight to external CDMOs and other vendors. Help establish scalable regulatory CMC processes and approaches in a growing biotech organization. You will thrive in this role if you: Have a bachelor’s degree in a life sciences discipline or equivalent (advanced degree preferred). 7+ years of hands-on experience in regulatory CMC. Demonstrated experience leading CMC regulatory strategy for cell therapies. Experience working in early phase development (IND/CTA-enabling through Phase 1/2) with pragmatic, stage-appropriate CMC approaches. Proven ability to lead cross-functional workstreams, manage multiple priorities, and deliver high-quality outputs under tight timelines. Strong interest in longevity and aging biology, and motivation to work in a field where the playbook is still being written. It’s a bonus if you: Have experience working on iPSC-derived cell therapies. Have experience across multiple product modalities (e.g., cell/gene therapy, small molecules, biologics, etc.). Experience in late phase development (e.g., Phase 3) and registrational/commercial settings. Extensive global experience, including in non-traditional jurisdictions and emerging markets. \n $200,000 - $240,000 a year At Retro, we don’t use titles. New hires join as a “Member of X Team.” Depending on experience, this role is approximate to Director level. Total compensation also includes generous equity and benefits including: - Medical, dental, and vision insurance for you and your family - 401(k) plan with 4% matching - Unlimited time off and 10 company holidays per year - Paid parental leave - Annual learning & development stipend - Monthly longevity stipend - Free lunch and snacks \n We take pride in cultivating an environment that fosters collaboration, open communication, and authenticity. We believe that great results are best delivered by a highly creative team working in concert. We are an equal opportunity employer; we do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We are diverse in background and singular in mission.

Responsibilities

This role is accountable for the regulatory Chemistry, Manufacturing, and Controls (CMC) activities for all company programs, which include both cell therapies and small molecules, requiring the development and execution of global CMC regulatory strategies. The lead will prepare CMC dossiers for major submissions like INDs/CTAs and marketing applications, and serve as the primary regulatory liaison with health authorities for all CMC communications.