She/ he must have hands- on Biopharmaceutical industry experience in -
a) Development of purification processes for MAbs, fusion proteins, glyco- proteins - 1lt scale to 20ltscale
b) Analysis and de- bottlenecking of methods developed, results obtained
c) Hands- on experience in developing processes with AKTA chromatography instruments, TFF/ HFfiltration systems
d) Maintaining GLP records, identifying and incorporating the latest chromatography technologies intodevelopment programs
e) Individual will also be expected to document work in laboratory notebook.
f) Expected to be team player with potential leadership qualities