Inviting Applications interested working as Individual Contributor with 7 to 11 Years Experiences into Pharmaceutical Drug Regulatory Affairs preferably M.Pharm/Pharm.D/Ph.D/ any equivalent Providing experiences with regulatory submissions and approval processes in 1 or more major markets.
Experience in global/matrix environment or cross-functional teams. line extension.
Preferred in HA negotiations/Labelling knowledge. Operational expertise matrix management, Strong Interpersonal, communication, negotiation and problem solving skills. Preparation of regulatory maintenance submissions, variations, renewals and wave submissions as per global regulatory plan.
Basic organizational awareness (e.g, interrelationship of departments, business priorities). Work Location: Chennai
Experience in regulatory and knowledge in drug/blologic development. Expertise on new application/post marketing/LCM/
Please send your CV to tushar.tulapurkar@pfizer.com with Job title as "Manage Drug Regulatory Affairs" in subject line
