Intas Pharmaceuticals Ltd, Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors. A variety of initiatives in Research and Development, patents and ANDA filing, NDDS, quality manufacturing support, along with approvals by regulatory authorities of many countries has made Intas a global healthcare provider. Pioneering efforts in providing medications for both chronic and acute medical conditions, has truly led Intas live up to its corporate line Expressions for a Healthy Life.
opportunities with Intas Pharmaceuticals
Walk In Interview
Date: Saturday, 1st October 2022
Time: 10:00 Am to 03:00 PM
Venue: Intas Pharmaceutical Ltd. Corporate House, Near Sola bridge, S.G. Highway, Thaltej, Ahmedabad, Gujarat, India – 380054.
1. Executive/ Sr. Executive
Function: IRA – EU Variations
Qualification: B.Pharm/ M.Pharm
Eligibility: 1-5 years of experience
· Should be well versed in identifying, compiling & submitting the EU variation (specifically Quality & Safety variations) through the agency portal.
· Involved in CRF Evaluation
· Regulatory text preparation for agency submission
· Coordination with countries for national approval and national text preparation.
2. Executive/Sr. Executive
Function: Accord – RA (EU Artwork & Labelling)
Qualification: B.Pharm/M.Pharm/M.Sc
Eligibility: 1-5 years of experience
· Expertise in Artwork Preparation & Changes
· CRF Evaluation, Development of Production information (SPC/PIL/Label)
· Submission of Bromi/article 61(3) to MHRA for mock-up changes
· Review various site transfer/ In-license Artwork
· Co-ordination with studio and third parties for artwork preparation
3. Executive/Sr. Executive
Function: QA – FDA & DCGI (Regulatory Work)
Qualification: B.Pharm/M.Pharm/M.Sc
Eligibility: 1-5 years of experience
· Expertise in formulation & Biotech molecule registration with FDCA / DCGI, Involve in BE NOC for Export, Import application, Registration of various forms (Form -29, form 41, form CT 16, form CT 11, etc.), M&M & CT /BE application/Written confirmation certificate/GMP Inclusion/FDCA Application/COPP & FSC Applications, Filling dossers for the neighbor country like NEPAL.
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