Master degree in Pharmacology / Clinical Pharmacology / Pharmacy Practice / Clinical Research. OR Pharm.D/ MBBS/BDS from a recognized university / institute.

M.Sc./M.Pharm/M.S. in Chemistry / Analytical Chemistry / Pharmaceutical Chemistry/ Pharmacognosy / Natural Products Chemistry/ Biotechnology from a recognized university or equivalent.

First Class Post Graduate Degree including integrated PG degree or Second Class Post Graduate Degree including integrated PG degree with PhD

A first Class B.Pharmacy degree with a Masters degree (M.Pharm) in appropriate branch of specialization in Pharmacy. A PCI recognized Pharm.D degree holder shall also be eligible for the posts of Assistant Professor in the subjects of pathophysiology, pharmacology and pharmacy practice. 

Masters Degree in Public Health / Life Sciences / Clinical Research / Social Sciences / Epidemiology. PhD in a relevant stream mentioned above.

Doctoral Degree in Science from a recognized University or equivalent : Extensive experience in organic synthesis of small molecules for medicinal chemistry.

First-class postgraduate degree including the integrated PG degree. Second-class postgraduate degree, including the integrated PG degree with Ph.D.

Maintain robust governance for label changes triggered by safety signals, clinical/CMC updates, and regulatory intelligence; ensure harmonized global implementation timelines and traceability.

For more than 60 years. Ipca has been a crucial healthcare partner in over 120 countries across the 6 continents.

Hands on experience in HPLC, GC, dissolution, raw material testing, water sampling, weight analysis, and stability studies for injectables.

MedPlus One of the most trusted gateways to medicines and general provision With an aim to eradicate fake and ineffective medicines, and supply high-quality medicines in India, MedPlus was launched in 2006 in Hyderabad.

Bachelors in life science/healthcare required; Advanced degree or equivalent education / degree in life sciences / healthcare preferred (PhD/MD/PharmD/ Masters).

Looking for a Clinical Data Management Professional who thrives in a dynamic, international environment and brings a strong commitment to data quality and regulatory compliance.

Applications are invited for engagement of JRF under the GSBTM funded project entitled Investigating the therapeutic synergism of stem cell therapy and GHRH receptor analogue in post- stroke neuronal regeneration and management of vasogenic edema in the Department of Pharmacology and Toxicology, NIPER-Ahmedabad.

Analysis of RM-PM or IP-FP and handling of HPLC (Waters and SHIMADZU), GC(Agilent) is must

Preparation and updation of SOPs, BMRs, Log books, protocols and compliance thereof with training of people on the same.  Handling and monitoring of Environmental monitoring systemsystem.

This is a high-impact leadership opportunity to shape and drive enterprise-wide project governance across R&D and Manufacturing. Strong exposure to R&D, Drug Substance & Drug Product Manufacturing projects in Biologies Proven expertise in Program / Portfolio Management.

Support initiatives to maintain or improve quality performance and compliance of operational activities including risk management, health authority reporting, IT systems