Founded in 1849, Pfizer is the worlds premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.
Post : Regulatory Affairs professionals
Inviting applications from experienced & aspiring RA professionals for authoring & review of high quality Clinical/ Non-clinical/ CMC dossier content for New Registrations & Post-Approval Variations/ Licence Maintenance with Global Health Authorities.
Minimum Postgraduate in Pharmacy / Life Sciences
2-15 Years in Pharmaceutical Regulatory Affairs function; experienced in authoring & review of high quality regulatory submissions (INDs/ IMPDs/ NDAs/ ANDAs/ MAAs/ Post-approval variations) in Global markets (US, EU, Canada, AnZ & RoW) for Small Molecules (Sterile injectables, OSDs, etc.), Biologies/ Biosimilars, Vaccines & Devices. For Vizag based positions experience in CMC authoring for sterile injectable formulations is preferable.
Walk-in drive at Vizag on 20th November 2022 (9:00 am to 6:00 pm 1ST)
Venue : Fairfield By Marriott, KSR Prime, R&B Junction, Visakhapatnam - 530018, Andhra Pradesh
Interested candidates can share their resumes with Indiatalentacquisition@pfizer.com with the job title ‘Regulatory Affairs' in the subject line
See All Other Jobs in our Database