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
Job Description:
1.Preparing registration documents (Dossiers) for semi regulated market (Philippines, Vietnam & Ukraine).2.Having knowledge of regulatory requirement and procedures for Europe, Asian countries and sound understanding of following.
Desired Profile:
Prepare & Reviewed documents like BMR, BPR, STP, Specifications, labeling review (artwork), PIL comparison, F & D, Process Validation Protocol and Process Validation Reports. Introductory knowledge of Patents. Prior art searching/Family searching
Additional Information:
Experience: 1-2 Years
Location: Delhi, NCR
Compensation: Best in the industry
Education: B.Pharm, M.Pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
Email your resume to, hrd@brawnlabs.com
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