– Conduct stability studies of intermediates and active subtances as per predefined protocol , data compilation and evaluation as per ICH guidelines.
– Analysis of finished products as per the specifications, MoA and data compilation.
– Analytical method validation protocol , execution and final report preparation.
– Analytical method transfer
– Write standard operation procedures, analyticcal tests methods, protocols/reports for various analytical projects , or stability reports, when required.
– Review of data generated by chemist
– OOS and investigation reports
– To ensure that all the work is carried out in compliance with the required standards, conforming to company, cGMP, SOPs, regulatory regulations and guidelines, safety and evironmental guidelines.
Candidates will need to show evidence of the following :
*All fields are required/Todos los campos necesarios
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