Company Jobs

M.Sc. / B.Pharma. Operating equipment reactors, Sparkler Filter, Candle Filters, Centrifuge, Dryers as per SOP. Knowledge of GMP, cGMP, Data Integrity in USFDA and MHRA regulatory API manufacturing plants. Lupin pharma

To prepare and review new product documents like material requirement sheet, master formula card, bill of material, risk assessment reports, scale up protocol and reports, exhibit/ trial batch manufacturing record and exhibit protocols and reports etc.

Demonstrated experience managing, coaching, and developing clinical and medical professionals within a matrixed and cross-functional environment

Review and check the quality of the site and study documents to submit with IRB/EC central, local, hospital committee and HA/RA.

Develops and maintains clinical software Risk Management Files that include risk management plans, hazard analyses, risk assessments and post market surveillance.

Design and develop innovative formulations for solid oral dosage forms (Tablets / Capsules / Pellets) and injectable dosage forms. 

As a subject matter expert, you would be leading the workshop discussions on configurations with concerned business leads, understand & document business requirements. Solution designing, problem solving and working closely with other leads / consultants on a project assignment would be part of core responsibilities in this role.

Gathers, analyzes and documents user requirements for various business initiatives. Liaisons with IT and ensures requirements are appropriately translated into design specifications for systems and reports. Thermo Fisher Scientific

Ipca has been a crucial healthcare partner in over 120 countries across the 6 continents. We are a fully-integrated pharmaceutical company that manufactures over 350 formulations and 80 APIs for various therapeutic segments.