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Contractual Analytical Method Development Jobs (NOW HIRING)

Iambic Therapeutics, Inc

$224K - $310K/yr

Lead analytical method development, validation, transfer, lifecycle management, and troubleshooting across DS and DP, ensuring methods are fit for purpose, scientifically sound, and aligned with ...

Abbott

Method Development Scientist

Santa Rosa, CA · On-site

$90K - $180K/yr

Career development with an international company where you can grow the career you dream of ... Troubleshoot existing analytical methods * Author, review, and verify validation protocols and ...

Abbott

Method Development Scientist

Santa Rosa, CA · On-site

$90K - $180K/yr

Career development with an international company where you can grow the career you dream of ... Troubleshoot existing analytical methods * Author, review, and verify validation protocols and ...

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How much do contractual analytical method development jobs pay per year?

As of Sep 11, 2026, the average yearly pay for contractual analytical method development in the United States is $73,187.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,000.00 and $88,000.00 per year, depending on experience, location, and employer.

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Contractual Analytical Method Development jobs near you

Director, Analytical Development

Cambridge, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$185K - $240K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago

Job description

Responsibilities:
  • Lead analytical development strategy, priorities, roadmap; develop phase-appropriate, risk-based analytical assays and potency testing for iPSC-derived cell therapy products.
  • Recruit/manage/train/mentor Analytical Development staff.
  • Lead analytical development and method transfer to support iPSC expansion/differentiation in GMP manufacturing across the product lifecycle.
  • Oversee development/authoring/review/approval of SOPs, test methods, and qualification documentation supporting GMP and QC.
  • Act as SME for analytical development; lead technology transfer (in-process, release, product characterization) to CDMOs and CTLs.
  • Resolve complex QC testing issues during clinical production at CDMOs (person-in-plant support as needed).
  • Develop/review/approve analytical development source documents; provide CMC oversight for regulatory submissions; support regulatory responses and influence analytical strategy.
  • Lead CTL due diligence, evaluation, and selection; support CDMO selection due diligence.
  • Drive continuous improvement; support budget/resource/capital planning.
  • Partner cross-functionally (Regulatory, Quality, CDMOs, CTLs, R&D) and perform other assigned duties.
Minimum requirements:
  • 15+ years (BS) OR 13+ years (MS) OR 10+ years (PhD) biotech/pharma experience in cell/gene therapy; 7+ years managerial experience.
  • Expertise in cell therapy analytical methods (potency assays, flow cytometry-based assays, product characterization); method development/optimization/qualification/transfer.
  • Hands-on characterization (flow cytometry, RT-PCR, ddPCR); safety assays for lot release (endotoxin, mycoplasma, sterility, rapid release).
  • Analytical control strategies/specifications; stability studies per ICH and shelf-life setting.
  • Potency assay development/strategy for cell therapy; experience with CDMOs/CTLs.
  • Regulatory/CMC filings experience; strong analytical/problem-solving, communication/technical writing/presentation, urgency/accountability, teamwork, and cross-functional collaboration.
Preferred qualifications:
  • PhD/MS in relevant fields; iPSC-derived analytical method development/qualification experience.
  • Whole genome sequencing, bioinformatics pipeline, scRNA-seq experience.
Compensation/benefits:
  • Salary range: $185,000-$240,000.
  • Comprehensive benefits (medical/dental/vision/prescription, wellness resources, 401k/ESPP, paid time off & paid parental leave, disability, etc.).
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