Scientist, Analytical Sciences & Technology
Not Disclosed•Full-TimeOn-site
location_on506, West Manlius Street, Village of East Syracuse, Town of DeWitt, Onondaga County, New York, 13057, United States
ECLARO is partnering with a leader in the Biopharmaceutical Industry to find a Scientist, Analytical Science & Technology. This client is dedicated to delivering life-changing healthcare solutions by providing quality, innovative, and affordable medicines that make a difference in the lives of patients worldwide.
This position offers a dynamic, fast-paced, and entrepreneurial environment where you will be part of a diverse group focused on inclusivity and safety. As a Scientist within the Analytical Science and Technology team, you will support the full lifecycle of analytical methods, including development, qualification, validation, and technical transfer for biologics drug substance and product samples.
You will execute non-GMP testing, stability studies, reference standard qualification, and comparability studies to support clinical and commercial GMP manufacturing. The role involves a blend of laboratory and office work, with occasional presence in a classified GMP manufacturing environment. Your work will directly contribute to process development, characterization, and technical advancements in protein biotherapeutics.
If you are up to the challenge and interested in this rewarding opportunity, please contact Paul Quibuyen to discuss the next steps.
ECLARO values diversity and is an Equal Opportunity Employer. We do not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.
Work model: On-site
506, West Manlius Street, Village of East Syracuse, Town of DeWitt, Onondaga County, New York, 13057, United States
Town of DeWitt, New York
Experience across the analytical method lifecycle in protein biotherapeutics for a variety of methodologies and instrumentation used in the testing and characterization of raw materials, excipients, in-process, drug substance, and drug product samples including HPLC / UPLC methods and various other analytical techniques (i.e., qPCR, ELISA, CE-SDS, iCIEF, SDS-PAGE, UV-VIS, western blotting, mass spectrometry, and cell-based assays). Working knowledge and experience in the biopharmaceutical development process, GMP, PAT, CMC and regulatory guidance, ICH guidelines, and compendial requirements. Experience authoring, validating, and coordinating timely transfer of test methods with and to Quality Control laboratories. Demonstrated history of continuous improvement.
Skills: HPLC, Uplc, QPCR, Elisa, Ce-SDS, Icief, SDS-Page, Uv-Vis, Western Blotting, Mass Spectrometry.
Education: B.S. in Biology, Chemistry, Biotechnology, or equivalent area of related study; M.S. with 0-5 years experience (alternative to Bachelor's); Ph.D. with 0-5 years experience (alternative to Bachelor's).
