About this role
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