Job Description
Job Description
Prepare, review, and maintain Artwork-related activities for India Region Formulations in compliance with regulatory and corporate requirements.
Prepare and review of specification and STP of Raw material, Packing Material and Drug Product.
Update and manage all required QMS and documentation activities in Veeva Vault, ensuring data integrity and timely compliance.
Perform audits as and when required and provide support in the preparation and finalization of audit reports (US and IR Formulation).
Review raw data and analytical reports of contract manufacturing products to ensure accuracy, compliance, and adherence to approved specifications.
Work Experience
8-12 years in relevant area as mentioned in the Job description
Education
Graduation
Post Graduation in Pharmacy or Science
Competencies
