SIRE Life Sciences
As a pioneering bio-pharmaceutical company at the forefront of cancer immunotherapy, this company is dedicated to developing innovative and transformative treatments. Joining the team means becoming part of a cutting-edge organization committed to revolutionizing cancer care.
In this role you will be part of the QA Operations Review & Disposition department. Where you will use your QA skills for reviewing, identifying, and communicating QC data and Processes.
-You will examine quality control data for in process and finished products
-Review records in digital and paper format
-Use the environmental monitoring tool to obtain information for reports
-Preform various quality tasks in a GMP environment
-MBO or Bachelor degree
-At least 1-2 years’ experience in a highly regulated (GMP) environment
-Experience with computerized (e.g. ERP/EBR/LIMS) applications
-Previous involvement in the pharmaceutical sector or a related biotechnology industry would be a plus