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 : Associate / Senior Associate / Associate Manager / Manager / Principal Manager
Inviting applications from both experienced & aspiring RA professionals for authoring & review of high quality Clinical / Non-clinical / CMC dossier content for New Registrations & Post-Approval Variations / License Maintenance.
Preferred Experience :
• 2-15 Years in Pharmaceutical industry with major experience in Global Regulatory Affairs function.
• Authoring and / or contributing line to Clinical/ Non- clinical/ CMC content for DMFs/ INDs/IMPDs/ NDAs/ ANDAs/MAAs/Post-approval variations/ Supplements for Global markets.
Candidates with relevant technical experience in Pharma R&D, Tech Transfer, Quality & Manufacturing can also apply, and will be considered based on merit and potential.
Work Location : Ahmedabad, Chennai, Mumbai & Vizag (Hybrid Work Model)
Walk-in drive at Hyderabad on 11th and 12th March 2023 (9:00 am to 6:00 pm IST)
Venue : Pfizer Limited, Ground Floor - Accord Blu (No.8-2-610/68/1,2,3 Road No-10 Banjara Hills, Hyderabad 500034
Interested candidates may please send their resumes to indiatalentacquisition@pfizer.com or tushar.tulapurkar@pfizer.com
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