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12 Openings PAREXEL Regulatory Affairs Jobs 2023: Apply Now @Bengaluru

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Are you looking for Parexel Regulatory Affairs Jobs in 2023, The new jobs at Parexel are out now. Apply by following out below link but before that check out the Position, Key responsibilities, Roles, Qualifications, and experience as given below.

PAREXEL Regulatory Affairs Jobs

About Company:

PAREXEL has bееn a stеadfast supportеr of thе Bio-Tеch and Pharmacеutical sеctors, contributing to thе advancеmеnt of nеw drugs and mеdical trеatmеnts on a global scalе. Rеnownеd as a lеading worldwidе providеr of biopharmacеutical sеrvicеs, PAREXEL offеrs еxpеrtisе-drivеn contract rеsеarch, mеdical communications, and consultancy sеrvicеs across a divеrsе array of thеrapеutic domains within thе pharmacеutical, biotеchnology, and mеdical dеvicе industriеs.

PAREXEL Regulatory Affairs Jobs

PAREXEL Regulatory Affairs Jobs 2023 Overview:

OrganizationPAREXEL (Jobs for Experienced)
Job IDR0000003109
Position AvailableSenior Regulatory Affairs Associate at PAREXEL
RoleSenior Regulatory Affairs Associate
Candidate QualificationsCandidates should possess a Bachelor’s or Master’s degree in Pharmacy or Life Sciences
ExperienceA minimum of 5 to 6 years of relevant experience
Official Websitehttps://www.parexel.com/
Applying Last DateSeptember 20th, 2023
Job LocationBengaluru
Other Regulatory Affairs JobsCheck now
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PAREXEL Regulatory Affairs Jobs Overview:

  • This role involves overseeing CMC activities related to the manufacturing and quality control of Small Molecules.
  • Responsibilities include creating submission dossiers for various purposes, such as Approval variations.
  • The role requires a comprehensive understanding of regulations and guidance from the EU/WHO/US, ensuring meticulous review and data compilation to meet appropriate standards.
  • Experience in CTD update and authoring (CTD Module 1, 2 & 3), managing Health Authorities’ requests, handling US & CA Annual reports, Renewals, PQVAR, and APR, as well as assessing Change Controls and associated technical documentation, is essential.
  • Strong project management and communication skills, along with familiarity with the Veeva tool, are also desirable.

Additional Information:

Additional QualificationsBachelor’s or Master’s degree in Pharmacy, Life Sciences
Industry TypePharmaceuticals / Healthcare / Clinical Research
Application Deadline20.09.2023
HomepageGo here

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