Job Description

Planning /Analysis (Routine and 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.
Analytical Method development as per current SOP/guideline wherever required.
Regulatory query/Plant Query related analysis for different products.
To follow Good Laboratories practice while working.
Documentation and compliance and review of data generated on all analytical activities as per the GLP/GMP norms and to keep working place neat and clean.
Method transfer at plant.
Method equivalency, method verification, pharmaceutical equivalency analysis of Pharmacopeial method.
Preparation/review of various documents like method transfer waiver, method equivalency report, cleaning validation report SOP, T-STP/FP STP etc.
Coordination with team members, superiors and subordinates within the group and across all relevant groups (customers) to achieve target timelines.
Procuring of columns, reagents and miscellaneous items for analytical product development/support.
Whenever required give training to subordinates/colleagues to upgrade their knowledge and current requirements.
Work Experience
3 to 5 years of experience
Education
Masters in Analytical Chemistry or Analytical Chemistry
Post Graduation in Pharmacy or Analytical Chemistry
Competencies