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.
Post : RA professionals
Inviting applications from both experienced & aspiring RA professionals for authoring & review of high quality CMC dossier content for New Registrations & Post-Approval Variations/ Licence Maintenance.
Preferred Experience
• 2-15 Years in Pharmaceutical industry with major experience in Global Regulatory Affairs function.
• Authoring and/or contributing line to CMC content for DMFs/ INDs/ IMPDs/ NDAs/ BLAs/ ANDAs/ MAAs/ Post-approval variations/ Supplements and Medical Device Design History File/ Technical File/ Design Dossiser for Global markets.
• Candidates with relevant technical experience in Pharma R&D, Tech Transfer, Quality & Manufacturing, aspiring for Regulatory role can also apply, and will be considered based on merit and potential.
Work Model : Hybrid
Work Location : Ahmedabad, Chennai & Vizag
Walk in drive
Date & Time : 28th Oct, 2023 (9:00 am to 6:00 pm 1ST)
Venue : Pfizer Healthcare India (P) Ltd., Emerald Building, # 237, Anna Salai, Chennai - 600006
Interested applicants may send resumes to indiatalentacquisition@pfizer.com with the job title 'Global Regulatory Sciences * in the subject line.
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