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Principal Scientist, Analytical Development, Oligo and Small Molecule

Praxis Precision Medicines, Inc. · United States - Remote

Advances oligonucleotide and small molecule programs through analytical method development, validation, troubleshooting, and GMP testing while establishing scalable control strategies with internal and external partners.

About this role

Location: This position may be performed remotely, but requires the flexibility and willingness to travel as needed. Position Summary The Principal Scientist, Analytical Development will play a critical role in advancing Praxis' clinical and commercial pipeline by translating analytical strategies from development into manufacturing across our virtual network of CMOs and external partners. This role is particularly focused on advancing oligonucleotide-based therapeutics, while also supporting small molecule programs across the portfolio. The individual will bring deep expertise in analytical method development, qualification, validation, troubleshooting, and GMP testing for oligonucleotide drug substances and drug products, with the ability to apply phase-appropriate analytical strategies across multiple modalities. This is a highly cross-functional, hands-on leadership role requiring close partnership with Drug Substance, Drug Product, Quality, Regulatory, and Manufacturing teams to ensure robust, scalable, and compliant analytical control strategies. The successful candidate will help shape an agile, forward-looking analytical development function capable of supporting innovative CNS therapies from early development through commercialization. Primary Responsibilities Serve as Analytical Lead across CMC programs, with primary responsibility for oligonucleotide analytical development activities and support for small molecule programs Lead analytical method development, qualification, validation, transfer, and GMP testing activities across internal teams and external partners Drive technical troubleshooting, data interpretation, method lifecycle management, and review of analytical documentation including validation reports, stability reports, specifications, and CoAs Design and implement phase-appropriate analytical control strategies, specifications, and stability programs for oligonucleotide and small molecule drug substances and drug products Direct and manage CRO/CMO analytical partners to ensure high-quality execution, strong communication, and continuous operational improvement Collaborate cross-functionally to strengthen CMC operations, improve processes, and establish scalable technical and business practices across the analy

The employer's own description, as posted on their site. Apply on Praxis Precision Medicines, Inc.'s site ↗

oligonucleotide · analyticalmethods · gmp · smallmolecule · cdmo

Role
Other
Remote policy
fully-remote
Team
CMC
Region
Americas
Posted
2026-01-21
First seen
2026-11-07
Last seen alive
2026-11-07
Last verified
2026-11-07
Verification
AI-verified
Board
greenhouse
Report expired / not remote

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