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.
Open Positions
Research Scientist I – Solid-State & Preformulation
MS in Chemistry, Pharmaceutical Science or related field, 1-2 years of experience, strong communication and interpersonal skills
Senior Scientist or Associate Principal Scientist, LBA Platforms
Ph.D., M.Sc., M.A., B.A., in Biology, Immunology, Chemistry, Pharmacology, or other related scientific fields required
Manager/ Director of Quality Assurance
10+ years of experience in regulatory affairs, Bachelor's degree in biological, chemical, or physical sciences, and ability to provide regulatory leadership and guidance
HR Operations Manager
3-5 years of HR experience, with strong focus on HR operations, payroll, benefits, and compliance
Sr Scientist/ Associate Principal Scientist, LCMS Platforms
Ph.D. in a related scientific field and a minimum of 4 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