1. To comply with the implemented Quality management system as per ISO/IEC 17025: 2017, satisfying the requirement of regulatory agencies, accreditation bodies and customers.
2. To ensure laboratory safety, Data Integrity, Positive Documentation Practices, Good laboratory Practices are in line of implemented quality management system.
3. You shall keep yourself & team members abreast with latest changes in applicable regulations.
4. To maintain confidentiality of Laboratory’s information related to customers & organization and impartiality throughout your association with organization.
5.
6. To arrange and keep updated Analytical methods, Standards, and CRMs.
7. To ensure critical supplies are evaluated before these are in use.
8. To ensure,
Lab equipment are periodically calibrated & working. Maintenance schedule is available and effective, intermediate checks are performed as per defined schedule.
9. To ensure the validity of the test results by participating in ILC/PT programs.
10. Sample management before and after analysis as per applicable Lab procedure.
Any other task/activity assigned by management as & when required basis.