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Senior Scientist - Analytical Chemistry, Purification

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Satomic
Full Time position
Listed on 2026-07-26
Job specializations:
  • Research/Development
    Research Scientist
Salary/Wage Range or Industry Benchmark: 140000 - 160000 USD Yearly USD 140000.00 160000.00 YEAR
Job Description & How to Apply Below

Senior Scientist - Analytical Chemistry, Purification

About Satomic

Satomic’s mission is to close the gap from idea to molecule with faster navigation of chemical space. We are building an automated chemistry platform that integrates laboratory robotics, software, and AI to transform small-molecule synthesis and drug discovery.

This role is critical to Satomic’s mission. By isolating and delivering pure compounds quickly and reliably, you make more of that chemical space reachable, so our partners can focus on the hardest challenges in drug discovery and human health.

We are seeking an experienced analytical chemist to own, develop, and run Satomic's chromatography-based purification fleet with SFC as the primary technique, LC in support, using mass spectrometry as primary for detection and fraction collection. This role is central to Satomic's mission: purification is a bottleneck and our throughput targets demand a fleet that runs as a coordinated, automation-friendly system built for throughput rather than as individual instruments.

The successful candidate will develop, optimize, and standardize high-throughput, mass-directed purification methods and workflows, from fraction collection logic through post-purification data and sample handling. The work centers on SFC and LC purification, with a strong emphasis on SFC and on mass-directed purification, to deliver high-quality compounds and data that accelerate drug discovery efforts. You will keep the fleet running through preventive maintenance and fast troubleshooting, and partner closely with our software and automation teams to scale the purification capabilities.

This is a hands‑on, lab‑based position for a candidate who thrives in high throughput environments and is motivated to develop purification methodologies that are robust, scalable, and innovative while prioritizing rigorous data quality standards and sample integrity.

Expected Outcomes By 30 days, you will have:
  • Fully onboarded to all company policies, lab operations, and safety protocols
  • Achieved proficiency operating the SFC and reverse‑phase LC fleet, running both analytical and preparative methods independently
  • Mapped the current end‑to‑end purification workflow (sample submission → method selection → run → fraction collection → analysis → evaporation -> consolidation -> reporting) and identified the top 3 throughput bottlenecks
  • Begun running routine purifications and contributing to the standing sample queue
By 90 days, you will have:
  • Sustained throughput of ≥50 samples per instrument per day on at least one preparative SFC and one preparative LC system, with documented purity and recovery metrics
  • Developed and validated a standardized method set (generic gradients, column selections, modifier choices) that covers ≥80% of small‑molecule samples without per‑sample method development
  • Authored standard operating procedures for instrument operation, fraction collection logic, and routine maintenance for each instrument class
  • Designed and tested partner‑facing post‑purification QC methods for outgoing products
  • Partnered with the software/automation team to integrate purification data flow with Analytical Studio (or equivalent) for automated submission, tracking, and reporting
  • Established minimum evaporation times for varying volumes of collected fractions from LC and SFC purifications, enabling process optimization
  • Defined fraction consolidation logic, taking into consideration tradeoffs between purity, yield, and transfer process logistics
By 1 year, you will have:
  • Achieved sustained fleet‑wide throughput of ~96 samples per instrument per day across all 6 preparative systems, with ≥90% scheduled uptime
  • Built and deployed an automated purification workflow (queue management, automated fraction analysis, and structured data handoff); identified and integrated further automation that minimizes hands‑on work per sample beyond submission
  • Reduced average purification turnaround time (sample submitted → purified compound delivered) by a measurable amount versus the 90‑day baseline, with results quantified and reported
  • Established a maintenance and consumables program (columns, seals, pumps, frits, ESI…
Position Requirements
10+ Years work experience
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