ICMR-National Institute of Immunohaematology was established in the year 1957 with an aim to conduct multidisciplinary research related to Immunohaematology offer diagnostic services and provide training to medical and non medical professionals in the field of haematology, Immunology, genetics and conduct awareness programmes on haematological disorders.
At Wipro, the safety, health and well being of our employees is of paramount importance and over the past several weeks we have taken a series of preventive measures to protect our employees from the Coronavirus outbreak. Given the evolving situation, we have advised our employees to work from home wherever feasible and if their role allows them to do so. Wipro offices will remain open.
Post : Drug safety analyst - Literature specialist
B.Pharm, M.Pharm, Msc; Lead the Bio- PK team to plan and execute BA BE studies for various regulatory markets. Manage the designing of PK studies for demonstrating bioequivalence for solid, liquid, topical and specialized dosage forms including parental.
M.Sc, M.Pharm; Experience must include analysis of Raw Material, In-Process, finished goods, Stability Testing and Stability sample handling Tablets / Capsules. Handling of HPLC, dissolution and other sophisticated instruments.
Diploma in Pharmacy and 3 months training in Pharmacy along with Registration with Central or State Pharmacy Council duly allotted Registration Number. One year experience in a hospital/ Dispensary is essential.
This position will support and manage the regulatory activities associated with the Chemistry, Manufacturing and Controls for New Drug Applications across globe. Regulatory activities focus on filing activities/query responses/post approval changes as suggested across globe.
This position provides medical and scientific expertise for regulatory submissions and implies in-depth expertise within medical science, with primary goal of authoring clinical and non-clinical expert reports and summaries supporting new submissions of Generics, Innovative and Medis organizations in international markets
Analysis of Raw material, Stability and Finished product samples, must have hands on experience of instruments like, HPLC, GC, UV, KF, ICPMS & IR etc. QC investigation and QMS
Ph.D. in the area of Pharmaceutics/ Pharmaceutical Sciences/ Pharmacy/ Formulations/ Pharmaceutical Technology/ Industrial Pharmacy or equivalent. Ph.D. completed or Thesis submitted candidates can also apply.