Cadila Pharmaceuticals is an Indian multinational pharmaceutical group based in Ahmedabad, Gujarat, India. With more than 6 decades of experience, the companys integrated operations focus on manufacturing products ranging from API's-Intermediates, finished formulations, OTC-Food Supplements, Biotechnology Products and pharmaceutical Machinery. Cadila Pharmaceuticals manufacturing facilities are approved by International bodies such as WHO-GMP, UK-MHRA, USFDA-API, TGA-Australia, and AIFA-Italy. The company's international operation of is spread across 58 countries including the Americas, Japan, Asia, CIS and Africa.
Post : Executive to Manager
Number of Positions : 10
Qualification : B.Pharm / M.Pharm
Experience : 3 to 13 Years
Location : Dholka, Ahmedabad
Department : Regulatory Affairs
Job Description
• Collaborate and manage all relevant regulatory activities related to registration of products in ROW /EU/AU/NZ/CA Markets countries
• Review of technical documents
• Preparation and review of registration, renewal dossiers and variation documents as per current guidance applicable in respective countries
• Timely response to customer and regulatory queries
Timings : 10 AM to 3 PM | Date: 09/01/2022 (Sunday)
Walk-In Venue : Cadila Pharmaceuticals Ltd. Corporate Campus,
Sarkhej-Dholka Road, Bhat, Ahmedabad-382210
Interested candidate can share updated resume on mamta.pitale@cadilapharma.co.in or apeksha.langhanoja@cplbio.com
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