Medical device manufacturer specializing in glaucoma and corneal treatments
Glaukos manufactures implants and devices for glaucoma, corneal, and retinal disorders across a 1,000–5,000-person organization. The tech stack reflects a heavily regulated medical-device operation: Oracle PLM, Veeva (clinical/quality), SolidWorks (CAD), and compliance-focused tools (CDISC SDTM/ADaM for data standards, Helix ALM for traceability). Hiring spans manufacturing, research, sales, and healthcare roles in steady volume, with notable leadership gaps in regulatory affairs and clinical research—priorities that align with their published pain points around GMP compliance, medical-device regulation, and clinical enrollment.
Notable leadership hires: Area Director, Regulatory Affairs Director, Clinical Research Director
Glaukos develops and manufactures novel therapies for glaucoma, corneal disorders, and retinal diseases. The company serves ophthalmologists and surgical centers with implantable devices and procedural support, spanning minimally invasive glaucoma surgery (MIGS), corneal crosslinking, and emerging retinal treatments. Operations are centered in Aliso Viejo, California, with hiring also active in the Netherlands. The organization runs clinical research programs, surgical training labs, and quality-system initiatives alongside manufacturing and regulatory functions.
Glaukos uses Oracle (ERP/PLM), Veeva (quality/clinical), SolidWorks (design), CDISC standards (clinical data), Salesforce (CRM), Perforce (version control), Altium and AutoCAD (engineering), and SAS (analytics). The stack is typical of regulated medical-device manufacturers.
Glaukos is actively recruiting in the United States and Netherlands.
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