April 2025

B.Pharm with minimum 01 year of experience OR D.Pharm with minimum 03 years experience. Experience in Dispensary, Pharmacy of the Hospital having minimum 200 beds. Candidate should be prepared to work in shift duties, including night shift. Registration with State Pharmacy Council with duly allotted Registration Number is mandatory. Experience of working on computerized system desirable.

First-class post-graduate degree included the integrated PG degree OR Second-class post-graduate degree included the integrated PG degree with Ph.D. The Role of Extra Domain A Fibronectin in NETosis-Mediated Non-Ischemic Cardiac Hypertrophy 

M.Sc in Zoology, Biochemistry, Botany, Molecular Biology, Biotechnology, Microbiology, Life Science from a recognized University or M.Sc in Forensic Science

The Clinical Research Lead will oversee and manage clinical research activities within the organization. This role involves designing, implementing, and monitoring clinical trials to ensure they meet regulatory requirements and organizational goals.

Provide strategic guidance and expertise in oncology for the development and execution of medical affairs plans focusing on Lung Cancer, GU Cancers and Hematology portfolio. Collaborate with cross-functional teams to support the successful launch and commercialization of oncology products.

To assist establishing a system in accordance with Good Manufacturing practice guidelines and responsible for follow established , new procedures, new procedures, maintaining and updating existing procedures in the department.

Research experience, knowledge in extraction and isolation techniques chromatography purification, HPLC, etc and characterization of natural products and their modifications. M.Sc, M.S. in Chemistry, Organic Chemistry, Natural Products Chemistry, Medicinal Chemistry, Pharmaceutical Chemistry from a recognized university or equivalent.

Evaluates new market complaints daily and communicates them to the various manufacturing partners, determines the criticality of complaints and makes appropriate recommendations. Escalates critical complaints and those with the potential to affect an entire batch or multiple batches. 

This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.