- Written confirmation or EDQM
- Ensure stability studies ,data integrity and f unctioning of HPLC ,GC,FTIR ,UV and microbiological sections
- Collaborate with cross-functional teams to resolve quality issues and improve overall product quality.
- Develop and implement corrective actions plans to address non-conformities found during audits.
Desired Candidate Profile
- 10-15 years of experience in pharmaceutical industry with expertise in HPLC analysis, GC, UV, IR, Stability, Micro etc...