Coordinatelaboratory equipmentactivity to satisfy demands

Commissionequipmentand prepare and execute IQ, OQ and PQ activitiesasrequired. 

Develop and implement best practices for laboratory activities. Creation and maintenance of Standard Operating Procedures, maintenance procedures and Health and Safety procedures.

Perform all necessary laboratory and ProductDevelopmenttesting and supply datarequiredfor FDA submissions. Equipment will include metallographic, optical microscopy, chemical and physical analysis, dimensional measurement, First Article Inspection, etc., of metals, polymers, etc., as required.

Conduct DOEs, capability studies, MSAs, Technical report writing, Technical support, e.g. workmanship standards, product quality issue resolution, quality control support, engineering support, e.g. ECN generation.