Teams at Pharmathen S.A.

Perform routine and non-routine microbiological tests on in-process, finished and environmental samples; maintain accurate test records and sample logs; investigate OOS results; support supplier and contract lab audits.

Perform routine and non-routine microbiological testing of in-process and finished products, raw materials, and environmental monitoring samples; conduct sterility testing; document results and maintain sample logs; investigate OOS results; participate in peer-review of analytical data and support supplier/contract lab audits.

Lead and oversee product quality lifecycle activities to ensure cGMP compliance and product release. Manage inspections, testing, investigations (OOS/OOT), validations, CAPAs, deviations, audits, documentation, stability and APQR oversight, training, and cross-functional quality integration to continuously improve product quality.