What are the responsibilities and job description for the Pharmaceutical QA Leader with Global Focus position at Cipla?
Job Description
As a Director QA, you will be responsible for developing, establishing, and maintaining a Quality Management System as per 21 CFR Part 11 requirements. You will ensure product quality of all manufactured and released products at the site and maintain the highest standard of data integrity.
You will also review and approve deviations, change controls, CAPA, complaints, and laboratory non-conformances. Additionally, you will be accountable for batch disposition based on testing results and ensure the facility's readiness for audits.
