Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Catalent’s San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of our Catalent Spray Drying technologies with downstream roller compaction capabilities to support the needs of our client’s most challenging compounds. The Scientist 3 in our Analytical Development group will lead analytical method development projects for small molecule, peptide, and amorphous drug products, with a strong focus on HPLC/UPLC stability-indicating methods, while ensuring GMP compliance and supporting analytical strategy, troubleshooting, and continuous improvement initiatives. The role combines hands-on laboratory work with potential supervision and mentoring responsibilities, as well as collaboration with QA/QC, customers, and cross-functional teams.
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Job Type
Full-time
Career Level
Senior