Posted:3 months ago|
Platform:
Work from Office
Full Time
Role & responsibilities : Separately Instrument operation of HPLC, Dissolution , UV Vis spectrophotometer ,KF , Balance etc.. Worked experience in WHO and regulatory approved company Audit exposure for WHO and regulatory agencies Documents preparation and review like SOP, Specification, STP ,Protocol-Reports etc.. Good knowledge in regulatory requirements in Documents preparation Good knowledge in computer , QC routine activities and pharmacopeial updating Preferred candidate profile : 2-3 Years of relevant experience in Pharma Plant. Perks and benefits : Best in Industry
Avery Pharmaceutical Pvt Ltd
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