Functions as GRS-CMC to assess/assist Global Regulatory Leads (GRLs) to define the Global Regulatory submission strategy and ensure timely and quality regulatory submissions pertaining to Post Approval Changes, Original Application/ Global Expansion and License Maintenance of new/ on-market Biosimilar product(s)/Biologics Product(s), Small molecule products. On market includes supporting manufacturing plants and compliance issue management.
Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
#LI-PFE
MNCJobsIndia.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.