Key Responsibilities
1. Principal Accountabilities :
- Assist in development and validation of new clinical chemistry assays.
- Prepare reagents and verify raw materials.
- Maintain accurate documentation as per ISO 13485 and ISO 9001 requirements.
- Analyze QC testing data and perform troubleshooting.
- Manage testing data, ensure proper data transfer, and predict logical outcomes.
2. KPIs (Indicative) :
Optimize clinical chemistry assays on fully-automated and semi-automated analyzers.Handle biochemistry analyzers (internal & external).Perform documentation and procurement-related activities.Validate lab instruments for newly developed products.🎓 Required Skills & Experience
M.Sc. in Biochemistry (preferred) or Biotechnology .3–4 years of experience in validation / verification of clinical chemistry products.Strong experience in handling fully and semi-auto biochemistry analyzers.Experience assisting in formulation preparations for clinical chemistry assays.Strong understanding of fundamental calculations, reagent roles, and assay principles.Knowledge of ISO documentation processes (ISO 13485, ISO 9001).📨 How to Apply?
Send your updated resume to : n.anshika@transasia.co.in
with the subject line :
Application for Sr. Executive – R&D (Biochemistry)