The Principal Quality Engineer , Medical Device position will be based in San Clemente, CA and will directly support the manufacture of innovative ocular medical devices. This role includes verifying successful transfer of products into manufacturing, the review and/or execution of validations (IQ/OQ/PQ), risk management activities, environmental monitoring, supporting qu

The position of Manufacturing Engineer is responsible for supporting manufacturing by developing, qualifying, implementing and maintaining manufacturing equipment, processes and procedures.This individual will also develop and lead projects to improve process efficiencies and cost savings. Job Requirements Support existing manufacturing product lines. Lead, coordinate and

CLINICAL DATA REVIEW AND EXECUTION Authoring of clinical data management documents such as data management plan, CRF completion guidelines, data review guidelines Responsible for the development of eCRF design and annotation, database design specifications and data review listings Responsible in the validation activities such as user acceptance testing (UAT) of clinical d

The Sr. Manager, Clinical Compliance , based in San Clemente, CA will be responsible for developing, leading, implementing and conducting strategies and activities to assure Glaukos Clinical Research remains in compliance with applicable regulations and laws maintaining a constant state of audit readiness. Internal clinical audits Develop an internal clinical audit progra