Regulatory Affairs
1 week ago
The role ensures timely preparation,review& sub of dossiers & maintains alignment with Indian regulatory requirements under CDSCO,DCGI& ICMR guideline
Lead the preparation,review & sub of regulatory dossiers(CTD/eCTD format)for DCGI,including Form 44
Required Candidate profile
T-exp yrs
CTC-Max12.00Lacs
Loc-Kandivali-Mumbai
Qual-B Pharma/M Pharm
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