Responsible for testing, approve or reject of the raw materials, packaging materials & finished - products, stability samples as per the committed time lines.
Handling failure investigation.
Documentation, QMS, adherence to quality norms and GMP.
Preparation of the Plant for regulatory audits, validation etc.
Ensure all relevant local documents are uploaded, reviewed & approved in the electronic documentation management system.
"Education & Experience"
Education : B. Pharm/ B.Sc (Chemistry)/ M. Pharm/ M.Sc (Chemistry)
Experience : 1 year and above
Working hour from (08:30) definitely until (17:00) definitely (If in cases, Employee able to work under shift assigned as per alternate job nature but working hour shall not exceed more than 08:00 hours.
"Rest Days & Holidays"
Alternate Saturday, every Sunday and public holiday will be closed.