How will you make an impact? The Senior Scientist II Biocompatibility is responsible for the design, execution (including monitoring) and reporting on in vitro and in vivo studies supporting the nonclinical development of new drug delivery devices, medical devices and enabling their testing in clinical studies. These studies include biocompatibility studies conducted in c

GLAUKOS REIMBURSEMENT LIAISON (GLAUCOMA) SOUTHERN CALIFORNIA 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 private and hospital affiliated i

GLAUKOS SR. REGIONAL ACADEMIC MANAGER (TEXAS) How will you make an impact? The Sr. Regional Academic Manager (RAM) is responsible for training, educating, and advancing Glaukos technologies into their assigned accounts. The RAM will attend surgeries and assist attending surgeons/fellows/residents in order to achieve the desired surgical outcomes for the patient. This will

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 MANUFACTURING ENGINEER (Burlington, MA) How will you make an impact? Performs a variety of manufacturing engineering activities on ocular related products including manufacturing scale up, development, and sustaining activities. Responsibilities include developing creative solutions to manufacturing problems, development and execution of process, equipment, and pr

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