GLAUKOS FACILITIES TECHNICIAN How will you make an impact? The Facilities Technician will perform a variety of work in the maintenance and repair of the global headquarters location in Aliso Viejo including tenant improvements (electrical, plumbing, carpentry, drywall, and painting) and janitorial as needed. This individual will also apply their skills in the preventive a

How will you make an impact? The Clinical Programmer I will, at the direction of the Lead Clinical Programmers, design clinical study databases, program edit checks, integrate external data sources, and model and deliver data reports, dashboards and datasets. The Clinical Programmer II works in coordination with the Lead Clinical Programmer, Data Management, Biostatistics

Serve as Quality Control Subject Matter Expert for assigned drug programs. Ensure that method development, transfer, and validations meet current ICH and other regulatory guidelines. Perform quality control activities (such as analytical validation protocol/report review and approval, specification review and approval, laboratory record review and release, etc.) to ensure

GLAUKOS DIRECTOR COPORATE ACCOUNTS GLAUCOMA (United States) How will you make an impact? The Director Corporate Accounts Glaucoma (DCAG) will seek to enhance the customer experience and position Glaukos as a leading partner within the ophthalmology space. The Director will maximize the utilization of the Glaukos glaucoma product portfolio, increasing revenue and developin

GLAUKOS REIMBURSEMENT LIAISON (CORNEAL HEALTH) Mid South Total Compensation $200 210k + RSUs How will you make an impact? The Reimbursement Liaison will serve as an expert in reimbursement policies, as well as patient and provider support, to ensure patients have access to Glaukos' sight saving technologies. The Reimbursement Liaison works with physician practices (both p

include all aspects of inspection (receiving, in process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc. What will you do? Receiving Inspection Receiving inspection of components following procedures, specifications and drawings. Utilize a variety of

Review key study documents produced by other functions (protocols, statistical analysis plans [SAPs], TFL shells, case report forms) and interact with Statisticians and other clinical team members to ensure programming requirements are understood. Follow SAPs, develop specifications and execute derivation algorithms for analysis dataset production. Follow the SDTM and ADa

The individual in this position will perform a variety of manufacturing technician and low level engineering design activities in support of Glaukos' ocular related products manufacturing activities. Responsibilities include building subassembly and top level assemblies for Glaukos stent systems, developing creative solutions to manufacturing problems, ensuring the proper

Quality System Interfacing with all departments to ensure the quality system is implemented and effective. Lead groups in improvement projects to ensure continued compliance of the quality system. Creating reports in Oracle Cloud and CATSWeb systems for CAPA Review Board, Management Review, CAPAs, and other trending requests. Maintaining existing modules within the Oracle

How will you make an impact? Responsible for assisting in the development, analysis, and execution of scientifically valid human research studies for medical devices developed by Glaukos Corporation. This job description attempts to capture only the primary and most identifiable tasks of this position. What will you do? Clinical Study Design and Execution Writes drafts of

How will you make an impact? Glaukos is a medical technology and pharmaceutical company that's advancing the treatment of ophthalmic diseases. At Glaukos, we are pioneering new treatments for chronic eye diseases and are focused on novel therapies for the treatment of glaucoma (market leader iStent inject W), corneal disorders and retinal diseases. Glaukos is looking for

Manage and coordinate manufacturing and supply chain activities in support of development, clinical and marketed products. Provide expertise in support of internal qualifications and process validations. Provide expertise in support of qualifications of CRO's, CMO's, CPO's, 3PL's and related vendors in support of product manufacturing and supply chain. Key contributor on

& Work Experience Design Control Working with development teams to assure Clear and concise user requirements, product specifications, plans, verification and validation studies, risk management strategies and other relevant design control deliverables, Test protocols that include qualified and repeatable test methods, appropriate risk based sample sizes and clear test ins

GLAUKOS #DareToDomore Director, Clinical Compliance Founded in 1998, Glaukos is publicly traded ophthalmic medical technology and pharmaceutical company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders and retinal diseases. Our global headquarters is in Aliso Viejo, California, and we have additional locations in t

Glaukos Practice Integration Liaison (Southeast) Total Targeted Compensation up to $250k #DaretoDream #DaretoLead #DaretoCare How will you make an impact? The Practice Integration Liaison's objective is to improve patient access and experience with the Glaukos family of products by assisting ophthalmology groups remove operational and organization barriers. The Practice L