About Sipra Labs: Sipra Labs Limited is a US FDA-approved Contract Research Organization providing end-to-end regulatory-compliant research and development services to the Pharmaceutical, Biotech, and Medical Devices industries for over 30 years.
Role & Responsibilities:
Perform HPLC-based testing of raw materials, in-process samples, and finished products per approved methods and pharmacopoeial monographs (IP/BP/USP). Support method validation, verification, and transfer activities. Maintain accurate, contemporaneous analytical records and instrument logbooks. Ensure compliance with cGMP, GLP, and Sipra Labs QMS requirements. Troubleshoot instrument and method-related deviations.
Preferred Candidate Profile:
B.Sc/M.Sc (Chemistry) or B.Pharm/M.Pharm with 2-5 years of hands-on HPLC experience in a pharmaceutical/CRO/analytical testing laboratory. Familiarity with cGMP documentation and pharmacopoeial testing required.