Process Engineer I Position Summary: Work Schedule: Monday-Friday, core hours 8am-4:30pm 100% on-site (San Diego) 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 Process Engineer I will execute basic setup, operation, troubleshooting, breakdown, and cleaning of designated small scale and pilot scale pharmaceutical manufacturing equipment under limited supervision. You will get exposure to equipment maintenance activities, conducting demonstration batches, evaluating the formulation, analysis of various product characteristics, technology transfer process to the manufacturing group, and batch record review process. You will be a key manufacturing member in the GMP (Good Manufacturing Practices) suites as subject matter expert for designated projects and revision of SOPs (Standard Operating Procedures). The Role: Experimental design and execution will be under a supervisor’s direction Prepare reports, summaries, and generate procedures and SOPs Limited client interaction and regular interdepartmental interaction Continuous development of pharmaceutical process knowledge Training on scientific techniques, GMPs, and technical writing Development of observation and problem-solving skills for experimental outcomes Other duties as assigned
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Entry Level