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Description: Job Description - Preparation of AMV/AMTP for cleaning and validations - Review of Specification and STP - Timely investigation of OOS/OOT results - Expoure to regulatory audits such as UDFDA, MHRA, ANVISA, PMDA etc. - Allocation of work to the team members - Co-ordinatiomn with LRP, QA, CQA - Responsible for LCM of derug products. Work Experience about 8 to 10 years Education Graduation in Chemistry Masters in Chemistry Competencies Strategic Agility Process Excellence Collaboration Innovation & Creativity Result Orientation Stakeholder Management Customer Centricity Developing Talent