1. To perform analytical method development of drug products for different tests like Assay/Dissolution/Degradation products/Residual solvents/water content by using advanced techniques like HPLC/GC/UV/KF

1. To perform documentation through the BIOVIA system to ensure data integrity, traceability, version control, audit trail compliance, and secure electronic record management in accordance with applicable quality and regulatory requirements.

1. Performing routine/initial analysis of drug products for market samples/query response.

1. Preparation of method development protocols, reports, method equivalency report and COA

1. To perform multimedia dissolution study and compatibility study and prepare report of the same.

1. Maintaining lab safety compliance during analysis

1. Maintaining GLP compliance in the laboratory.

1. Maintaining GDP in the laboratory.

Work Experience

0 to 5 Years

Education

Masters in Pharmacy or Analytical Chemistry

Competencies

📌 Research Associate : IRF Analytical (India)
🏢 LUPIN
📍 India