0 years
0 Lacs
Posted:1 week ago|
Platform:
On-site
Full Time
JOB RESPONSIBILITY
1) RESPONSIBLE FOR DOSSIER COMPILATION.
2) RESPONSIBLE FOR TENDER COMPILATION.
3) ENSURE TIMELY DELIVERY OF REGULATORY QUERY.
4) TO WORK WITH QUALITY STANDARDS AND ADHERENCE TO THE SYSTEM.
5) COMPLIANCE ( AUDIT / AUDIT READINESS) - SUPPORT IN SITE AUDIT READINESS AND COMPLIANCE TO RELEVANT TO RA FUNCTIONS PROCEDURES BASED ON INTERNAL / EXTERNAL AUDIT.
JOB REQUIREMENT
1) (2-4) YEARS OF WORK EXPERIENCE IN REGULATORY.
2) WHO / ROW COLLABORATIVE COUNTRIES HAVING KNOWLEDGE OF REGULATORY GUIDELINE VIZ ICH , EMEA, PIC.
CTC - (4.5 - 5 ) LPA
LOCATION ; MUMBAI (GOVANDI - WEST)
INDUSTRY - PHARMACEUTICAL MANUFACTURING
Maneesh Pharmaceuticals Limited
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