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Covalent Laboratories Private Limited is seeking a Quality Control Chemist to perform chemical analysis of raw materials, intermediates, APIs, stability samples and finished products per approved specifications, standard test methods and cGMP requirements. The role operates in a USFDA, EU-GMP and ISO 14001 certified facility and supports Cephalosporin production for global and domestic markets.
Prior experience in pharma QC is preferred.
12th October- 13th October, 9.30 AM - 2.00 PM
Contact - Mahesh Reddy(9100132004)
The Quality Control Chemist is responsible for performing chemical analysis of raw materials, intermediates, APIs, stability samples, and finished products as per approved specifications, standard test methods, and cGMP requirements.
Skills highlighted with ‘‘ are preferred keyskills
Covalent Laboratories Private Limited is an USFDA,EU-GMP & ISO 14001(2004) Certified & Reputed Pharmaceutical Company, pioneer & Leader of producing Cephalosporin products since 2003 in theGlobal/Domestic market.
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