BRAWN, with its inception barely 21 years back(1988) has today evolved into a fully integrated, healthcare group, marking its presence in India and dotting various major markets across the globe. With its claim of quality and certified with ISO 9001:2000, 13485, WHO : cGMP, BRAWN is proud to possess product registration with major health and govt. institutions throughout India and in many other countries worldwide.
Headed and represented by a team of skilled industry experts with impressive educational backgrounds and broad experience, BRAWN continues to spread its wings in expansion in the domestic as well as in the international markets with a vision beyond the existing horizon to stand among the leading Indian HealthCare Companies.
Post: Executive Regulatory Affairs
1. Preparation and submission of Dossiers for registration in regulated, semi regulated & non regulated countries.
2. Coordination with R&D, QA,QC & production for regulatory requirements.
Shall be responsible for taking the regulatory approvals for regulated, semi regulated and ROW.
Should have excellent technical expertise in regulatory and Quality Compliances
A team builder and lead the project to its succes based on timeline
Experience: 1-2 Years
Education: B.Pharm, M.Pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
End Date: 14th Oct., 2011
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