Job Description Execute defined Quality Control department activities including housekeeping, testing of raw materials, in process products and where appropriate, bulk drug substance, final products and stability products according to defined procedures and best cGMP work practice, Quality standards and metrics.
Role
Perform testing activities by following procedures and report results in timely manner of raw materials and in process samples and where assigned by the Team Leader, of bulk drug substances, final products and stability products applying cGMP and quality standards.
Check and review data in compliance with Data Integrity requirement.
Perform any stability study programme activities, storage of in process and final samples and retention samples management.
Ensure that PPE, consumable and material are available by maintaining adequate stock control.
Assist in coordination of incoming deliveries and dispatches.
Arrange subcontract of QC testing and dispatches to approved suppliers as appropriate.
Assist in document writing including procedure, investigation and deviation where training has been completed.
Ensure that all laboratory areas and surrounding QC facilities are cleaned and maintained in accordance with housekeeping procedure and processes and remain at an inspection ready state.