Scientist /Sr Scientist/ Associate Principal Scientist, LCMS Platforms
Crystal PharmatechCalifornia, United States
Posted November 6, 2025
110000 - 160000 USD year
Full Time
About the Company
Crystal Pharmatech is a specialized CRO/CDMO founded in 2010 that excels in crystal form and formulation services for small‑molecule drugs. With a global footprint that includes cGMP facilities in the United States, Canada, and China, the company has supported over 1,000 clients and more than 2,000 compounds, delivering expertise in solid‑state research, crystallization, pre‑formulation, formulation development, and manufacturing. Their integrated service portfolio spans developability assessment, solid‑form screening, formulation, and commercial manufacturing, all compliant with FDA, EMA, and NMPA standards. A distinctive feature is the Mol2Med program, a three‑step First‑Time‑Right approach that expedites lead compounds from optimization to Phase I by ensuring robust API forms and scalable processes. Crystal Pharmatech’s culture of precision, collaboration, and regulatory excellence positions it as a trusted partner for efficient, high‑quality drug development.
Job Description
Crystal Bio Solutions is a CRO providing global-standard services in GLP/GCLP bioanalysis and biomarker. Our clients include multinational pharmaceutical companies and biotech companies. The Bioanalysis & Biomarkers Department specializes in Method Development, Method Validation, GLP/GCLP Bioanalysis for PK, and biomarkers.
Requirements
- Ph.D., M.Sc., M.A., B.A., in Biology, Immunology, Chemistry, Pharmacology, or other related scientific fields required, including a minimum of 4+(Ph.D.), 9+(Master’s) or 12+(Bachelor’s) years of CRO/Pharma/Biotech experience.
- Hands-on experience and strong knowledge of GLP/GCLP bioanalysis.
- Experienced with GLP/GCLP LCMS method development and validation for PK and/or biomarker analysis.
- Functional experience utilizing LIMS and QMS systems for GLP/GCLP bioanalysis
- Established record of independent achievement of objectives and timelines while maintaining high work quality.
- Effective in team environments co-workers, managers, and clients
- Must be goal-oriented, compliance-ensured, quality-conscientious, and client-focused.
- Effective writing and communication skills are required.
- Experience in large molecule LCMS analysis (e.g. ADC, mAB, protein, peptide, oligonucleotide etc) preferred.
- Familiarity with additional bioanalytical platforms (e.g. LBA, PCR, Flow Cytometry) preferred.
- Supervisory experience in both project and talent (people) management is preferred.
Benefits
- 401(k)
- 401(k) matching
- Bonus based on performance
- Dental insurance
- Free food & snacks
- Health insurance
- Paid time off
- Parental leave
- Vision insurance
