Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), with its San Diego facility focusing 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, including preformulation testing, formulation and analytical development, cGMP manufacturing, clinical packaging, labeling, and worldwide distribution. The San Diego location is home to Catalent Spray Drying technologies with downstream roller compaction capabilities. The Manufacturing Technician I will be responsible for conducting Good Manufacturing Practices (cGMP) manufacturing of solid oral and liquid oral pharmaceutical dosage forms for Phase I and Phase II clinical trials. This role is a key member of a multi-site mission to deliver unparalleled service to clients and quality drug products to patients.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees