Senior Scientist I Analytical Development

Benefits

Parental leave

Not verified

Non-birth-parent leave

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Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

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Relocation assistance

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Childcare support

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Learning budget

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Verification

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Salary

$112K-$135K From the posting source

401(k) match

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Market context

U.S. role benchmark (BLS OEWS)

$111,944 U.S. median for this role

Projected growth (BLS Employment Projections)

+13.7% - Much faster than average

10% above the BLS role benchmark for data and ml aggregate.

Matched to SOC 15-1252 - Data and ML aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Data From the posting source

Seniority

Senior From the posting source

Schedule

Shift type

Not verified

Weekend work

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Company

Equity

Offered Verified - SEC 10-K source

Application

Cover letter

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Assessment

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Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Senior Scientist I Analytical Development South San Francisco Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. The small molecule CMC team is seeking highly motivated Sr. Scientist I of Analytical Dev e lopment to help build our dynamic small molecule CMC group at Alumis . The successful candidate will help to support the analytical development and quality control activities from the preclinical phase through late-stage clinical development. Having analytical development expertise and experience in working with CMOs/CTLs, coupled with thorough understanding of the associated quality and regulatory awareness are key assets. RESPONSIBILITIES Support development, validation , and transfer of analytical methods to support starting material, intermediate, drug substance and drug product testing at CMOs/CTLs Execute and/or support the in-house method development activities using UPLC/HPLC, LC-MS, KF, and dissolution instrumentation and technique s for Phase 1 to late-stage drug development Review CMO/CTL analytical data (in-process, release, and stability data), protocols and reports Trend stability and release data using statistical methods Assist in investigation for various non-conformance events at CMOs/CTLs Collaborate with CMC team, QA and CMOs /CTLs towards timely generation and approval of documents Communicate scientific results (oral and written) in a clear and concise manner within cross-functional teams Author technical reports and documents in support of regulatory filing Assist in

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