Walk in Interview at Intas SEZ For QC (HPLC FP Stability AMV)

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.
• Strong understanding of HPLC, FP, and AMV techniques for stability analysis.
• Proficiency in using software such as LIMS/Lotus Notes for data management.