Job Description

1. Product optimization of Lateral Flow Assay and Flow Through Assay.

2. Product complains verification, documentation and biological sample handling.

3. Daily instruments/equipment log book filling and handling.

4. COA, SOPs, Specification preparation, verification and submission to QA as per company QMS.

5. In process R&D and production check list preparation and verification.

6. New RM evaluation, execution and implementation in flow through system.

7. Daily collected Biological samples testing and qualification in FT, LFT and ELISA system.

8. Testing and evaluation of FT, LFT kits and comparative study with compare to market standard kits.

9. In House RM testing, Optimization & standardisation.

10. Documentation as per company QMS system and track the GDP & GLP.

11. Lab Instruments/Equipment handling, complain register, follow-up with maintenance team to ensure the equipment performance.

12. Daily Log book/...

Apply for this Position

Ready to join Meril? Click the button below to submit your application.

Submit Application