You will be responsible for adhering to GLP (Good Laboratory Practices) and safety practices, and ensuring compliance with the SOP (Standard Operating Procedure).
Your responsibilities include analysis of samples as assigned by the group leader, ensuring adherence to relevant SOPs and Standard Testing Protocols (STPs), and following online documentation and calculation practices.
You will also be responsible for authorized transactions in SAP and LIMS (Laboratory Information Management System), as well as the online reporting of any Out-of-Specification (OOS), Out-of-Trend (OOT), and incidents to the group leader.
You will be responsible for verifying that analytical results are conforming with specification limits.
You will maintain and monitor 5S practices in the laboratory, perform sample management for the team and handle any other responsibilities assigned by the team leader.
Qualification & Experience
5 to 8 years of experience in a laboratory setting, preferably in pharmaceutical or related industries