03 Oct
|
Intas
|
Ahmedabad
Roles and Responsibilities
- Conduct HPLC, FP, and AMV stability analysis for pharmaceutical products.
- Ensure compliance with cGMP guidelines during sample preparation and testing.
- Maintain accurate records of test results, reports, and data analysis.
- Collaborate with cross-functional teams to resolve issues related to product quality control.
- Participate in continuous improvement initiatives to enhance laboratory efficiency.
- 3-8 years of experience in Quality Control (QC) or similar role.
- MS/M.Sc(Science) degree from a recognized university.
- Robust understanding of HPLC, FP, and AMV techniques for stability analysis.
- Proficiency in using software such as LIMS/Lotus Notes for data management.
📌 Walk in Interview at Intas SEZ For QC (HPLC FP Stability AMV) (Ahmedabad)
🏢 Intas
📍 Ahmedabad