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Candidate should have knowledge of theoretical working principle of KF auto titrator, dissolution, spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC 

Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose

Experience in Pharmaceutical Company in Parental, responsible for line clearance activity, responsible for in process checks, responsible for sampling. Finished product checking before release, management and execution of process validation & media fill simulation.

Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.

OSD - Coating, Compression, Granulation, Ointment-External Preparation General Manufacturing and Sterile Manufacturing. IPQA - OSD and Injectable, AQA, APQR, Documentation, Validation, QMS, CQA, Artwork. Injectable, Aseptic, SIP, CIP, Batch Manufacturing, Bulk Manufacturing, Dry Powder, Oral Liquid. B.Pharm, B.Sc, M.Sc. HPLC Operating, Dissolution, Assay, RS, RM-Testing by HPLC, GLP HPLC Calibration, Finished Product Analysis By HPLC, PM Lab Testing 

B.Sc / M.Sc / B.Pharma / M.Pharma; Review HPLC methods, chromatograms, and system suitability. Ensure HPLC sequences comply with methods. Prepare and review IQ, OQ, and PQ for new instruments. Conduct pre-investigations for OOS, OOC, OOT, and lab incidents. To perform line clearance, FG Sample withdrawal, Online GMP Monitoring, To Support of Product and Process Validation

Diploma/D. Pharmacy/B. Pharmacy; Operating Granulation, Compression, Coating, Capsule Filling, Blister & Bottle Packing Equipment. Supervising Granulation & Packing Lines. Experience in Autoclave, Filling, Vial Washing, Packing Areas

M.Sc, M.Tech, B.Pharm having 2 to 6 years of experience of Biotech and Chemical Analysis e.g., Electrophoresis, Bioassay, HPLC & GC.

To Perform analytical activity of Development, Scale-up support, Method validation, Method transfer, Release, Stability, Drug product characterization, E&L study, In-Vitro study, routine analysis of inhalation dosage forms. M.Pharm, MSc