Candidate should be capable of operating Analytical instruments such as HPLC, GC,Dissolution Appratus, UV, IR, KF etc. should be aware and capable of Qualitative, Quantitative, Sample, Wet, Routine analysis of drug substances, intermediates, finished products, raw materials etc.
Supports to the Laboratory functions to handle Investigations, Deviation Management, Specifications ,test methods, method validations equipment qualifications ,internal audits and escalations if any.
Responsible for post approval submissions to Europe, Australia, New Zealand and Canada market. To provide Regulatory inputs during inspections by Regulatory authorities and Customer as and when required.
Post - Graduation in any discipline of life sciences from a Govt. recognized University or Institute with at least 60% marks in aggregate or equivalent grade for general category candidates.
B.Tech, M.Tech, M.Sc, MBA Preferably with B.Pharm or Masters. Should possess keen interest and drive for promoting technology innovation/ entrepreneurship.