Program Description

The diploma of pharmaceutical quality control program will provide student working knowledge of analytical instrumental techniques (HPLC, UV-Vis, FT-IR, GC and dissolution), computerized integrators and troubleshooting techniques, and how to use the US pharmacopeia and British Pharmacopoeia in detail. Also teaching students current Good Manufacturing Practices(cGMP), FDA and International Conference on Harmonization (ICH) guidelines, applicable standard operating procedures, analytical monographs, basic organic chemistry, analytical chemistry, Student will practice a variety of tests in the laboratory.

After finishing this course students will perform complex chemical and physical analysis on a wide range of pharmaceutical products in accordance with standards and established procedures.

Career Opportunities

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Perform testing on finished and semi-finished goods including tablets, capsules, liquid, raw materials, etc.
Familiar with lab instruments such as HPLC, UV-Vis, FT-IR, Dissolution, GC, TLC and wed chemistry
Compile records and interpret experimental or analytical results
Responsible for accurately maintaining lab instruments, equipment, notebooks and records to GLP (Good Laboratory Practice) standards
Review routine/non-routine supporting test data and results, including sample preparation records, chromatograms/graphs, logbooks, calculations, and datasheets. Enter results in SAP/LIMS, as needed
Lead and/or provide guidance on Phase 1 OOS laboratory investigations

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