Job description
Job description Perform testing on in-process samples, RMs, finished drug product, and stability study samples in support of production, packing release and regulatory filings. Reporting Structure: Reports to QC lab Supervisor Experience 3 - 6 years experience in a cGMP laboratory setting Familiar with cGMP and FDA requirements Bachelor s Degree in Chemistry or closely related degree. Perform analytical testing and release of in-process material, bulk drug substance, finished drug product, and …