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)