Live opening · Posted 7 days ago
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About the role
Description supplied by the original job listing.
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
Work arrangement
No
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