- Investigate and document Minor/Track & Trend deviations within GMP-regulated environments
- Perform root cause analysis (RCA) and collaborate cross-functionally to resolve quality issues
- Draft clear, accurate technical reports for scientific and non-technical audiences
- Track and manage quality records such as deviations, CAPAs, and material recalls
- Support continuous improvement and error prevention initiatives based on recurring issues
- Interact with QA, Supply Chain, and Warehouse teams to gather data and finalize investigations
- Dental insurance
- Health insurance
- Batch Records: 1 year (Required)
- SOPs: 1 year (Required)
- Capa: 1 year (Required)
- cGMP: 1 year (Required)