Senior Regulatory Affairs Specialist

Senior Regulatory Affairs SpecialistThe role of Regulatory Affairs Professional to handle:New Plant LicensingNew Products RegistrationDocumentation regarding new molecules registrationCorrespondence with DRAP for submissions, approvals, renewals and other affairsStrongs knowledge of DRAP regulations and pharmaceutical legislationExcellent regulatory writing and documentation skills.Experience Requirement:Candidates Having 5 to 7 years of relevant experience in any reputable organization in the same capacity will be preferred.