To develop, validate analytical methods to support the formulations development.
Implementation of QbD principle and tools to analytical methods for entire product lifecycle.
To handle analytical development for various dosage forms.
Preparing documentation of the analytical methods and Standard Testing Procedures
Analytical research, Analytical Method Validation and ICH Stability Testing.
Adept at supervising analytical work & documentation as per pharmaceutical industry regulations.
Expertise in analytical and method development, Method validation and method transfer activities for solid dosage formulations.
Expertise in preparation of protocols, reports & calculation sheets of validation, specifications, test procedures, SOPs for analytical activities and Investigation reports.
Maintaining basic laboratory systems and procedures related to cGMP/cGLP
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