About Relay Therapeutics
Backed by GV and SoftBank VF.
About the role
The range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate’s education, experience, skills and location.
What they're looking for
- Own the analytical strategy for drug substance programs at CDMOs, directing method development, validation, and troubleshooting to enable characterization, release, and stability testing of Relay clinical candidates
- Provide senior-level review and approval of method transfer/validation protocols, data sets, and reports, ensuring scientific rigor and regulatory readiness
- Hold accountability for QC testing oversight across analytical testing labs and DS manufacturing sites, including vendor performance and quality of deliverables
- Review and approve method qualification protocols and reports at external laboratories, serving as the final scientific authority on method suitability
- Direct the review and QC of raw data from third parties supporting batch release and stability, lead data trending efforts, proactively flag risks to the team, and drive resolution of issues
- Manage a portfolio of concurrent projects, prioritizing resources and timelines across programs in a fast-paced, evolving environment
More about this role
- You will lead and drive strategy for analytical method development and phase-appropriate method validation/transfer activities supporting full characterization of small molecule NCEs, from early development through late-stage/commercial readiness.
- Own the analytical strategy for drug substance programs at CDMOs, directing method development, validation, and troubleshooting to enable characterization, release, and stability testing of Relay clinical candidates.
- Provide senior-level review and approval of method transfer/validation protocols, data sets, and reports, ensuring scientific rigor and regulatory readiness.
- Hold accountability for QC testing oversight across analytical testing labs and DS manufacturing sites, including vendor performance and quality of deliverables.
- Review and approve method qualification protocols and reports at external laboratories, serving as the final scientific authority on method suitability.
- Direct the review and QC of raw data from third parties supporting batch release and stability; lead data trending efforts, proactively flag risks to the team, and drive resolution of issues.
- Manage a portfolio of concurrent projects, prioritizing...
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