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Accountable for regulatory CMC activities for Retro’s programs. Develop the regulatory CMC strategy and lead global plans. Lead the preparation of the CMC dossier for INDs/CTAs and amendments. Act as Retro’s regulatory liaison with health authorities for CMC. Lead health-authority meetings for CMC topics. Identify regulatory CMC risks and mitigation strategies. Bachelor’s degree in life sciences (advanced degree preferred). 7+ years of hands-on regulatory CMC experience. Experience leading CMC regulatory strategy for cell therapies. Experience in early phase development (IND/CTA through Phase 1/2). Lead cross-functional workstreams and deliver high-quality outputs on time. Strong interest in longevity and aging biology. 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.