About USP
The firm is more than 200 years of experience in producing the quality standards helping major bio-pharmaceutical firms in delivering high quality medicines to relieve many diseases. This is an organization supplying methods at free of cost for the product development and maintaining the standards. This is distributed across the globe serving mankind.
About the Job
Experience : 1-3 years with masters in Chemistry
Required exposure in General chapters understanding and GMP/ GLP environment and documentation
Knowledge in handling the instruments like UPLC, HPLC, GC_MS and FTIR
Handling of analytical method development and Validations of Drug substance and products.
Required to prepare the Protocol and reports.
Job Role
Project planning, execution, method development and validation according to set standards as USP guidelines, general chapters, SOPs and protocols
Able to design, review, and execution of method development experiments and perform method validation in accordance with laid down procedure.
Experience on chromatography (HPLC, GC) techniques.
Expertise on method development and validations (DS/DP/Excipients).
Responsible for preparation of method validation protocols and reports.
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Plan individually the project requirements and their completion within the timelines by coordinating with the supervisor and team.