Hyderabad

Masters, Integrated Masters Degree in Natural or Agricultural or Pharmaceutical Sciences from a recognized University OR Bachelors degree in Engineering or Technology or Medicine from a recognized University

This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent will support the reference standard program within the Global Biologics department. The incumbent in this role will focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards.

To participate in sample processing for PK, ADME assays and handling of LCMS/MS. Ability to adapt to the dynamic team environment. Processing of different matrices samples of PK studies. Optimization of test compounds manually as well as automated on LCMS/MS. M.Pharm in Pharmaceutical sciences, Pharmaceutical Analysis who has interest and passion for LC/MS related bioanalysis

Post-graduate degree including integrated PG degree such as M.S Pharm, M. Pharm, M.Sc, M. Tech or Equivalent with specialization in Biotechnology, Life Sciences, Pharmacology and Toxicology.

Must have hands on experience in working with chemical methods and handling instruments like Prep HPLC and HPLC. Expertise in HPLC & Prep HPLC method development and basic undersatnding in data interpretation of various analytical technique such as LCMS, GCMS, FTIR, UV-Visible, NMR etc is required.

Skilled scientist with expertise in trace level quantification of GTI/ Nitrosamines/Nitrites or similar impurities using LC-UV/FID, Ion chromatography and LCMS. Ensure all own activities are aligned with overall drug development process. Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC & Novartis Guidelines; Strategic and scientific contribution to Networks, target achievements according to net-work charter and annual objectives

Handling HPLC, GC, IP, FP, Stability Calibration of Analytical Instruments like HPLC, GC, UV, Dissolution etc.. Handling LCMS, ICPMS, PSD, AAS, XRD, Microbiology

Candidates with experience in Formulation QA RA, Analytical, Formulation R&D, and interested in advancing their career in RA ROW, are encouraged to apply.

Candidates should have hands-on experience of cell culture, recombinant protein expression and purification, molecular biology techniques, and handling of small laboratory animals.