Pfizer is the world's 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. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.
Post : RA professionals
Inviting applications from experienced & aspiring RA professionals for authoring & review of high quality Clinical/ Non-dinical/ CMC dossier content for New Registrations & Post-Approval Variations/ Licence Maintenance with Global Health Authorities.
Experience : 2-15 Years in Pharmaceutical Regulatory Affairs function; experienced in authoring & review of high quality regulatory submissions (INDs/ IMPDs/ NDAs/ANDAs/ MAAs/ Post-appeal variations) in Global markets (US. EU, Canada. AnZ & RoW) for Small Molecules (Sterile injectables. OSOs, etc.). Biologies/ Biosimilars, Vaccines & Devices.
Walk-in drive at Chennai Office on 12th and 13th November 2022 (9:00 am to 7:00 pm 1ST)
Venue : Pfizer Healthcare India Pvt.Ltd. Emerald Building. 237, Anna Salai. Chennai - 600006
Interested applicants can share their profiles with email@example.com with the job title 'Regulatory Affairs' in the subject line.
See All Other Jobs in our Database