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3.0 - 7.0 years

0 Lacs

vadodara, gujarat

On-site

As a candidate for this role, you will be responsible for working in accordance with organizational compliance requirements. Your main tasks will include developing methods for various quality attributes for complex injectable drug products such as Liposomes and Ophthalmic Drug products. You will also be in charge of performing method validation and verification, as well as analyzing drug products using a variety of analytical techniques including HPLC, GC, UV, and other relevant methods. In addition, you will be tasked with identifying, investigating, and troubleshooting issues as they arise. Your responsibilities will also involve conducting chemical analyses such as Extraction, Refluxing, Residue on ignition, Centrifuging, and Evaporation. Furthermore, you will be expected to prepare study templates, analytical method validation and verification reports, as well as protocols to support your findings. Overall, this role will require a high level of attention to detail, strong analytical skills, and the ability to work effectively within a regulated pharmaceutical environment.,

Posted 3 days ago

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