Walk in interview in Regulatory Affairs Department at Caplin Point
Caplin Point was established in 1990 to manufacture a range of ointments, creams and other external applications. The Company was listed in 1994 following its Initial Public Offering (IPO) which was oversubscribed 117 times, the proceeds of which were deployed in setting up a manufacturing facility at Pondicherry. Thereafter, the Company expanded its product range and increased its production capacity. The Company focused on the emerging markets of Latin America, Caribbean, Francophone and Southern Africa and is today one of the leading suppliers of Pharmaceuticals in these regions, with over 2800 product licenses across the globe.
Post : Exe., Sr.Exe., AM & DM
Department : Regulatory Affairs
Experience : 3 - 9yrs
• Preparation & Review of CTD dossiers.
• Preparation and review of post approval filings (Annual reports, CBE-O, CBE-30 and PAS)
• Review of artworks and updation of labels & patents.
• Review and finalize the API / IP/FP/ Excipients / PM specifications, BMR'sand Stability protocols/data.
Experience in US & EU Market (Injectables)
Work Location : Chennai
Send your CV's to firstname.lastname@example.org
Shortlisted Candidates will be called for Personal Interview.
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