1. Conduct in-process inspections, sampling, and verification activities during vaccine manufacturing.
2. Support investigations of deviations, non-conformances, and CAPA implementation.
3. Review, approve, and ensure accuracy of batch documentation, including manufacturing records and reports.
4. Assist in preparation for audits, inspections, and regulatory reviews.
5. Monitor environmental conditions and GMP compliance in manufacturing areas.
6. Collaborate with cross-functional teams including Manufacturing, QA/QC, and Engineering.
7. Facilitate training and awareness of GMP practices among shop-floor staff.
8. Support continuous improvement initiatives related to quality systems and processes.
Preferred candidate profile
Candidates having Vaccine experience will be considered.