Job Opportunities API

ABOUT THE ROLE We are a vibrant and intensely mission-driven team in San Francisco, comprising members from MIT, Harvard Medical School, Roche, ETH, and Dana-Farber. We value speed and rigor, coupled with excitement, drive, and a strong work ethic. In an early-stage environment, we value people who can bring clarity to open-ended problems, take ownership of the next steps, and follow through with energy. Capable Labs is a place for ambitious, high-integrity people who want to become dramatically better. You will be surrounded by people who care intensely about the work, get close feedback from the people making scientific and company-defining decisions, and have room to own increasingly important problems. We believe excellent work should be met with meaningful reward, ownership, and trust. Responsibility is earned through contribution, not title alone: anyone who demonstrates the judgment, rigor, and follow-through to move important work forward can earn meaningful scope.   WHAT YOU'LL DO - Execute and optimize small-molecule and peptide synthesis workflows, including route planning, reaction setup, workup, purification, analytical characterization, and sample preparation for biological testing. - Design, run, and troubleshoot organic reactions across medicinal chemistry programs, including functional group transformations, coupling chemistry, protecting group strategies, late-stage diversification, and parallel synthesis. - Run solid-phase and solution-phase synthesis workflows where useful, including resin-based chemistry, coupling/deprotection cycles, cleavage, crude analysis, purification, and final compound QC. - Troubleshoot challenging chemistry issues, including low conversion, poor selectivity, side products, decomposition, incomplete deprotection, solubility issues, purification challenges, and instrument downtime. - Purify and characterize compounds using analytical HPLC, prep HPLC, LC-MS, NMR, flash chromatography, SFC, and related methods; record identity, purity, yield, and batch-level QC data before handoff. - Prepare compounds for in vitro and in vivo studies, maintain rigorous experimental records, and communicate synthesis results, issues, timelines, and risks clearly to the team. - Support next-round compound design by contributing chemistry insight on synthetic feasibility, SAR, purity, yield, stability, solubility, and structure-property relationships.   WHO YOU ARE - You have hands-on chemistry experience and strong experimental judgment. You may come from any educational background; what matters is your ability to learn quickly and maintain a high standard for results. - You’re eager to own synthesis end-to-end: designing compounds, running reactions, purifying and characterizing them, and preparing them for testing with care and urgency. - You enjoy solving problems creatively, iterate quickly, and uphold scientific rigor. - You are interested in being close to the biological readout, understanding how compounds perform in vitro and in vivo, and leveraging potency and efficacy data to inform the next design cycle. - You demonstrate high initiative. When an instrument fails, a synthesis doesn't proceed as planned, or a handoff requires clarification, you proactively take ownership, troubleshoot efficiently, and ensure resolution.   PAY & BENEFITS - $90,000-$140,000 salary, plus equity options with an implied current value of approximately $50,000-$200,000 before exercise cost, taxes, dilution, and liquidity risk. - Compensation will depend on the skills, experience, and scope of impact you bring. If your background, experience, or compensation needs fall outside this range, we are still open to a conversation based on the scope and impact you could bring. - $500+ monthly wellness budget for training, supplements, coaching, recovery, or other tools that help you perform at your best. - Healthcare: We offer a broad range of medical, dental, and vision cover