M.Sc

Must be from Parenteral background & exposure to Aseptic vial, Bottle filling process is desirable. To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures. Sound technical knowledge of Aseptic area & Controlled area related activities.

As per the batch manufacturing procedures and packing protocols, samples such as in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples should be collected and submitted

Having Injectable Experience of Analysis of raw material. In-process, Finish products, Stability testing, Process validation. Hands on Experience of HPLC, GC, LBPC, Osmometer, KF Auto titrator and UV - Visible spectrometer, LIMS,QMS,Participate in Lab incident , OOS, OOT, Analysis of deviation.

This workshop is designed to empower faculty members, researchers, and postgraduate students with practical knowledge and skills for the ethical and effective use of Artificial Intelligence in academia and research. It offers comprehensive, hands-on training in utilizing advanced Al tools for literature review, research writing, manuscript development, data analysis, presentation, and responsible publishing practices.

M.Sc. in Chemistry or equivalent degree minimum of 55% marks or equivalent grade with specialization in Organic Chemistry.  Working experience in Industry or chemical research laboratory; Experience in Electro organic Chemistry and Natural Product Synthesis

AstraZeneca is committed to contributing to our broader society, and encourages an environment for talents from a broad diversity of backgrounds, providing equal opportunities for learning and growth. With this in mind, Project iDEA was created to connect students from diverse cultures, perspectives and ethnicities to the pharmaceutical industry.

Intas is expanding and evolving its Biopharmaceutical capabilities. We invite ambitious professionals to be a part of its future growth story.

 IPQA Mfg. & Packing, Shop floor activities, Review of equipment audit trails, BMR, BPR review, line clearance. Process Validation, equipment, Utility qualification.

Handling HPLC. Compilation of Raw Data for Review. Sampling and Release of Raw material and Packaging Mate. Analysis & preparation of water Trends.