Opening in Regulatory Affairs for Baroda site
Grade: Executive / Sr Executive
Experience: 3-7 years in
1) Compile registration dossiers for submission to various health authorities like – China, Canada, Europe, Australia/New Zealand, Japan and Israel.
2) Maintain life-cycle / post approval changes for drug product registration dossiers
Send your resume to: Hr.Tandalja@sunpharma.com
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