1. Analysis (Routine ,Stability and QBD analysis) of ongoing projects by performing analysis of various tests (e.g. Dissolution, assay, Related substances test, or as per requirement) within given Time

1. Analytical Method development as per current SOP/guideline wherever required.

1. Regulatory query/Plant Query related analysis for different products.

1. To follow Valuable Laboratories practice while working.

1. Documentation and compliance of data generated on all analytical activities as per the GLP/GMP norms and to keep working place neat and clean.

1. Effective utilization of all available resources like instruments, apparatus etc.

1. Method transfer at plant.

1. Method equivalency, method verification, pharmaceutical equivalency analysis of Pharmacopeial method.

1. Preparation of various documents like method transfer waiver, method equivalency report, cleaning validation report, SOP’s, T-STP/FP STP etc.

1. Maintenance of documentation as per the SOP according to the GLP practices.

1. To undergone training as per requirements to upgrade knowledge and current requirements.

Work Experience

2 to 6 years of relevant experience.

Education

Masters in Analytical Chemistry or Pharmacy

Competencies

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