Catalent’s San Diego, CA site is an early‑phase development facility supporting small‑molecule and peptide programs from preformulation through cGMP clinical manufacturing for oral and injectable dosage forms. The 68,000‑square‑foot site is a center of excellence for spray‑drying and bioavailability‑enhancement technologies, with integrated capabilities to advance challenging compounds rapidly into the clinic. We have an opportunity for a QC Chemist I to join our team. In this role, you will perform analytical techniques and standard laboratory practices to assess the quality of pharmaceutical products under cGMPs with limited supervision. This entry-level position offers the chance to broaden your analytical knowledge and learn common operations in a fast-paced, early-phase Quality Control group. You will work in a dynamic environment that values precision, collaboration, and continuous learning. Shift: Monday - Friday 8 AM - 4:30 PM Location: San Diego, CA 100% Onsite
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Job Type
Full-time
Career Level
Entry Level