. We are looking for a passionate and self-motivated fresher to join our Formulation & Development teamPrepare and maintain batch manufacturing records (BMRs),lab notebooks,and experimental reports ....view more
Analytical method development and validation shall be in line with required documentation as per cGMP / GLP requirements following the laid down Quality management procedures by CQAFace customer or re...view more
Timely query response submission to Distributor/ MOH. Review of documents for its correctness and compliance with respective regulatory guidelines (as per country requirement)....view more
Role & responsibilities * Data Entry and Updation in Regulatory Information Management System.* Dossier preparation (New/ Renewal/ Variations) for different countries.* Other RA Related Activities.Pe...view more