Description:
This role is responsible for conducting in-process and final product quality analyses and inspections in strict compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment. It operates within a structured quality management framework aligned with 21 CFR Part 210 and 211, ICH guidelines, and applicable Indian and international pharmaceutical regulations.
Essential Functions:
Additional Responsibilities:
Qualifications
Education:- B. Pharm B. Pharm - Required
- M. Pharm M. Pharm - Preferred
Experience:- 1 year or more in 1 - 4 Years
Specialized Knowledge: Licenses: