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Analytical Development Cell Therapy Jobs (NOW HIRING)

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Analytical Development Cell Therapy information

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How much do analytical development cell therapy jobs pay per year?

As of Sep 9, 2026, the average yearly pay for analytical development cell therapy in the United States is $74,986.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,000.00 and $93,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Analytical Development Cell Therapy job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $74,986 per year, or $36.1 per hour.

Director, Analytical Development

Cambridge, MA • On-site

Scorpion Therapeutics
51 - 200 employees

$200 - $250/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 4 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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