Drug Regulatory Affairs Jobs in Bangalore

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Regulatory Affairs Manager  

SurgeWay Biosciences - Bengaluru, Karnataka, India

spanning 40 years, SurgeWay is led by a dynamic young team that brings a professional approach and long-term business growth outlook. Our expertise in regulatory affairs, coupled with in-depth market

from: linkedin.com - 6 days ago

Regulatory Specialist  

Novo Nordisk - Bangalore, Karn, IN

Management and Coordination: Plan, coordinate, and project manage regulatory activities, including handling Change Requests, corrective and preventive actions (CAPA) cases, and representing Regulatory Affairs

from: Novo Nordisk - 17 days ago

Expert - Regulatory CMC  

Merck - Bengaluru

combination products . Minimum 5 years of experience in regulatory affairs in medical devices and drug / device combination Not disclosed INR

from: naukri.com - 27 days ago

Global Regulatory Submissions Manager  

Bengaluru / Bangalore, India

in Regulatory Affairs Excellent communication, organization and planning skills with an attention to detail Extensive experience in leading clinical trial applications at a regional/global level Direct project Not Mentioned

from: Monsterindia.com - 4 days ago

Senior Literature Specialist  

Bengaluru / Bangalore, India

Pharmaceutical industry experience (eg drug safety (desired), regulatory, clinical development, medical affairs) Working knowledge of key pharmacovigilance regulations and methodologies Good English language Not Mentioned

from: Monsterindia.com - More than 30 days ago

Drug Safety Associate  

Bengaluru / Bangalore, India

writing and Medical Coding. Ability to perform Quality Control checks and ensure Regulatory Affairs compliance. Knowledge of Pharmacy and experience in drug safety. Excellent attention to detail Not Mentioned

from: Monsterindia.com - More than 30 days ago

Scientific Writer, Medicines Innovation Hub, LCCI  

Bengaluru / Bangalore, India

writing, or regulatory affairs, within the pharmaceutical or medical device industry. Familiarity with Food and Drug Administration regulations, ICH guidelines, and other relevant regulations. Ability Not Mentioned

from: Monsterindia.com - 16 days ago

Associate Director - Materials  

Bengaluru / Bangalore, India

, regulatory, medical affairs, legal, commercial, and quality to achieve organizational goal to providing safe drug and medical device products to our global patient population. Act as a thought leader in global Not Mentioned

from: Monsterindia.com - More than 30 days ago


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