Demo

Sr. Scientist, Analytical Development

Kaye/Bassman International
Woburn, MA Full Time
POSTED ON 6/5/2026
AVAILABLE BEFORE 7/4/2026

The Opportunity

A rapidly growing, clinical-stage biotech company is hiring a Sr. Scientist to support Analytical Development and Quality Control for their peptide-based therapeutic programs. This is a highly visible, mentorship role for someone who can own and execute HPLC/UPLC, validation and method development based testing.


This position will play a key role in ensuring analytical readiness as programs advance through Phase 1 → Phase 2 and beyond.


What You’ll Own

  • Lead and execute HPLC/UPLC analytical methods supporting in-process, release, and stability testing
  • Drive chromatography workstreams including SEC and reverse-phase methods (primary focus)
  • Serve as the technical “go-to” for method troubleshooting, system performance issues, and investigation support
  • Support and/or lead method qualification and validation activities in a GMP-aligned environment
  • Provide oversight for routine QC testing, data review, and documentation practices
  • Write and maintain key technical documentation including SOPs, protocols, reports, and audit-ready records
  • Partner cross-functionally with teams spanning development, manufacturing, and quality
  • Mentor and guide junior scientists / associates while remaining highly hands-on in the lab


What We Looking For

  • Ph.D. in Analytical Chemistry, Biochemistry, or related field with a minimum of 4 years
  • Deep, practical experience with HPLC UPLC
  • Strong chromatography foundation (especially SEC RP)
  • Background in a GMP environment with direct exposure to method qualification/validation
  • Proven ability to troubleshoot and resolve real lab problems quickly (not just run methods)
  • Comfortable leading from the bench and supporting a growing team


Preferred Background

  • Experience working with peptides or complex therapeutic modalities
  • Experience from environments like CDMOs/CMOs or high-throughput GMP labs
  • Exposure to early clinical-stage programs (Phase 1/2)


Why This Role

  • High visibility on a growing team
  • Opportunity to impact analytical strategy and QC execution during a critical scale-up period
  • Strong cross-functional exposure in a fast-moving environment

Salary : $125,000 - $145,000

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