Senior Scientist - Small Molecule Analytics & QC

Uncover; Bothell, Northern (WA, KY); Hybrid; USD 170,000 - 196,000; Full time

Job summary

Immunome, Inc. is seeking a Principal Scientist, Analytical Development and QC, Small Molecule, to support multiple programs. You will develop complex analytical methods, validate them, transfer to manufacturing, and manage lifecycle activities in collaboration with CDMOs and internal teams.

The role requires strong expertise in LC/GC/LC-MSMS, NMR, Karl Fischer, and spectroscopy, with experience in regulatory submissions and GMP documentation. Occasional travel may be required.

Qualifications

• Ph.D. with 3 years' experience, MS with 8 years, or BS with 10 years in biopharma.
• Degree in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or related fields preferred.
• Experience developing and transferring analytical methods for small molecules in cGMP environments.
• Experience overseeing CDMOs/CROs and regulatory submissions.

Responsibilities

• Develop and execute phase-appropriate analytical methods for LP intermediates.
• Lead method development, qualification, validation, transfer, troubleshooting, and lifecycle management.
• Collaborate with external labs and ensure alignment with timelines and regulatory standards.
• Author and review CMC sections of regulatory submissions and GMP documentation.

Skills

LC

GC

LC-MSMS

NMR

Karl Fischer

Spectroscopy

Analytical lifecycle management

Data integrity

Problem solving

Education

Ph.D. analytical chemistry

M.S. in chemistry/pharma

B.S. in chemistry

Tools

CDMO oversight

cGMP environments

Regulatory submissions

Job description

Immunome, Inc. is seeking a Principal Scientist, Analytical Development and QC, Small Molecule, to support multiple programs. You will develop complex analytical methods, validate them, transfer to manufacturing, and manage lifecycle activities in collaboration with CDMOs and internal teams.

The role requires strong expertise in LC/GC/LC-MSMS, NMR, Karl Fischer, and spectroscopy, with experience in regulatory submissions and GMP documentation. Occasional travel may be required.