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Interview for Regulatory Affairs ROW and EU at BDR Pharmaceuticals

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Interview for Regulatory Affairs ROW and EU at BDR Pharmaceuticals

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.

Walk in Interview

Regulatory Affairs ROW - Assistant Manager
• Minimum 8 to 12 years of relevant experience required.
• Hands on Experience on Regulatory Affairs of various ROW markets.
• Lead the team for day to day RA activity.

Regulatory Affairs ROW- Officer
• Minimum 1 to 3 years of relevant experience required
• Require experience on RA row market.
• Dossier submission for regulatory market.


Regulatory Affairs EU - Lead
• Minimum 10 to 14 years of relevant experience required
• 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.

Regulatory Affairs EU - Executive
• Minimum 3 to 7 years of relevant experience required
• 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.


Warehouse-Technician (OSD + Injectable)
• Minimum 2 to 6 years of relevant experience required
• To receive all RM, PM, solvent and consumable material received from vendor as per define procedure.
• Dispensing of RM, PM, solvent and consumable material as per define procedure.
• Receipt, Raw Material and packing Material Dispensing, Handling of Cold Storage Material, Balance Calibration activity.

Walk in Interview
Date : 15th February 2025
Venue : BDR Pharmaceuticals International Private Limited, Baska, Gujarat

Preferred : Experience with regulated market products and USFDA approved plant.
Kindly note : Walk in drive is only for the mentioned opening. 

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