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Job for M.Pharm, B.Pharm as Regulatory Affairs professionals at BDR Pharma

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Job for M.Pharm, B.Pharm as Regulatory Affairs professionals at BDR Pharma

BDR Group of companies has grown steadily and become a house-hold name in the pharmaceutical Industry over the last 15 years, in both domestic and international arenas. We are recognized as a niche player in manufacturing of Pharmaceutical APIs and for our renowned new age formulations. The group is complemented majorly by its two companies - BDR Pharmaceuticals International Pvt Ltd and BDR Life sciences Pvt. Ltd, each one having stamped its own supremacy in respective fields, i.e. API and formulation manufacturing, respectively.

Post : Executive / Sr Executive , Officer / Sr Officer, Asst Manager / Dy Manager

Asst Manager / Dy Manager - RA -US, EU, Canada, Australia and Brazil Markets
Regulatory Affairs professionals with 5 to 8 years of experience in regulatory strategy, dossier review, and submission for the US, EU, and Brazil markets. This role requires a deep understanding of CMC requirements and the ability to lead the regulatory strategy for various dosage forms, including complex injectables and ophthalmic products.
Location : Baska, Halol
Experience : 5-8 years in RA (Preferably US/EU Market)
Qualification : M.Pharm / B Pharm
Executive / Sr Executive - RA -US, EU, Health Canada, Australia and Brazil Markets
Regulatory Affairs professionals with 3 to 5 years of experience in managing CMC aspects, dossier compilation, and submission for US, EU, and Brazil markets. This role will focus on leading the preparation of high-quality regulatory submissions and managing complex CMC documentation for various dosage forms, including solid or injectable products.
Location : Baska, Halol
Experience : 3-5 years in RA (Preferably US/EU Market)
Qualification : M.Pharm / B.Pharm
Officer / Sr Officer - RA -US, EU, Health Canada, Australia and Brazil Markets
Candidates with 0 up to 3 years of experience in CMC (Chemistry, Manufacturing, and Controls) aspects for pharmaceutical products. The role involves preparation, review, and submission of dossiers in compliance with regulatory requirements across the US, EU, and Brazil markets. 
Location : Baska, Halol
Experience : 0-3 years in RA (Preferably US/EU Market)
Qualification : M.Pharm / B Pharm 

Pharma industry background 


Share your Resume at : hrd@bdrpharma.com by 25th October 2024

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