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Analytical Method Development Scientist Jobs in Boston, MA

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Analytical Method Development Scientist information

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$24

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$70

How much do analytical method development scientist jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for analytical method development scientist in Boston, MA is $45.71, according to ZipRecruiter salary data. Most workers in this role earn between $34.23 and $52.74 per hour, depending on experience, location, and employer.

What does an analytical method development scientist do?

An Analytical Method Development Scientist is responsible for designing, developing, and validating analytical methods used to test and analyze chemical compounds, pharmaceuticals, or other materials. They ensure that the methods are accurate, reliable, and compliant with regulatory standards. This role involves working with advanced laboratory instruments, troubleshooting analytical issues, and documenting procedures for use in research, quality control, or manufacturing environments.

What are the key skills and qualifications needed to thrive as an analytical method development scientist?

To thrive as an Analytical Method Development Scientist, a strong background in chemistry, analytical techniques, and method validation—often supported by a relevant degree in chemistry or pharmaceutical sciences—is essential. Familiarity with laboratory instrumentation such as HPLC, GC, MS, and software for data analysis, as well as knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for success in this role. These skills ensure reliable method development, regulatory compliance, and effective collaboration within multidisciplinary scientific teams.

What are the typical challenges faced by an analytical method development scientist when transferring methods to quality control or manufacturing teams?

One common challenge for Analytical Method Development Scientists is ensuring that newly developed analytical methods are robust and reproducible when transferred to quality control or manufacturing teams. Differences in equipment, sample matrices, or operator technique can impact results, so thorough method validation and clear documentation are essential. Scientists often work closely with cross-functional teams to provide training, troubleshoot issues, and adapt protocols as needed. Successfully managing these transitions helps maintain product quality and regulatory compliance.

What is the difference between Analytical Method Development Scientist vs Analytical Chemist?

AspectAnalytical Method Development ScientistAnalytical Chemist
Primary FocusDeveloping and validating new analytical methodsPerforming routine analysis and testing
Work EnvironmentResearch labs, R&D departmentsQuality control labs, manufacturing facilities
CredentialsBachelor's or Master's in Chemistry or related field; experience in method developmentBachelor's degree in Chemistry or related field; experience in analytical testing

While both roles involve analytical testing, the Analytical Method Development Scientist primarily focuses on creating and validating new analytical methods, often in research settings. In contrast, the Analytical Chemist typically performs routine testing to ensure product quality in manufacturing or quality control labs.

What are popular job titles related to Analytical Method Development Scientist jobs in Boston, MA?

For Analytical Method Development Scientist jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Analytical Method Development Scientist jobs in Boston, MA look for?

The top searched job categories for Analytical Method Development Scientist jobs in Boston, MA are:

Infographic showing various Analytical Method Development Scientist job openings in Boston, MA as of September 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $95,081 per year, or $45.7 per hour.

Director, Analytical Development

Cambridge, MA • On-site

Scorpion Therapeutics
51 - 200 employees

$185K - $240K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 7 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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