Teva pharmaceuticals • Apprenticeship • Mumbai
2025-09-29 – 2026-04-30
Industry: Pharmaceutical • Headline: CTD/eCTD, cGMP, GLP, ICH guidelines, US FDA, EMA
Documentation & Compliance <br>▸ Ensured 100% SOP compliance across all analytical activities within a cGMP/GLP regulated R&D <br>environment. <br>▸ Maintained laboratory documentation, including analytical logbooks, instrument usage records, ELN <br>documentation and test result records while ensuring compliance with ALCOA++ data integrity principles and <br>Good Documentation Practices. <br>Analytical Testing & Scientific Data Generation <br>▸ Performed assay, dissolution, and blend uniformity testing on formulations including Lisinopril, Simvastatin, <br>Enzalutamide, Hydrochlorothiazide, Sertraline, and Carvedilol, with sample analysis performed using HPLC <br>and UV spectrophotometry. <br>▸ Conducted dissolution testing of generic formulations to support in-vitro performance evaluation and <br>bioequivalence studies. <br>▸ Ensured compliance with approved STPs, SOPs, GLP guidelines, and laboratory safety procedures during <br>analytical testing activities. <br>▸ Performed instrument troubleshooting and maintained equipment records to support accurate and timely <br>analysis.
