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Glaukos

Medical devices for glaucoma treatment

Business Systems Manager-Quality

Enterprise ApplicationsConfirmed live in the last 24 hours
Full-time$107.7k - $134.6k

About the Job

Requirements

  • A bachelor's degree in Information Systems, Computer Science, Engineering, Life Sciences, Quality, Business, or a related discipline is required.
  • Seven or more years of experience supporting business systems within a regulated environment.
  • Five or more years of experience supporting Quality Management Systems, electronic Quality Management Systems, or related validated applications.
  • Hands-on experience administering or supporting at least one enterprise quality system, such as Veeva, TrackWise, Maximo, or comparable Quality and compliance platforms.
  • Experience leading system implementations, upgrades, integrations, migrations, vendor delivery, and computerized system validation activities.
  • Strong understanding of Quality processes, including CAPA, complaints, audits, change control, document control, training management, nonconformance management, supplier quality, and equipment or asset quality processes.
  • Working knowledge of computerized system validation, 21 CFR Part 11, data integrity requirements, risk-based validation methodologies, and controlled systems lifecycle practices.
  • Understanding of integrations among Quality platforms, ERP systems, manufacturing systems, training systems, asset management systems, and reporting tools.
  • Strong project management, business analysis, problem-solving, and process improvement capabilities.
  • Ability to translate business, quality, and compliance needs into clear, actionable technology requirements and solutions.
  • Ability to lead cross-functional initiatives, manage competing priorities, and drive adoption of new processes and technology.
  • Ability to work in a standard office environment and use computer-based systems for extended periods.

Responsibilities

  • Serve as the business systems owner and subject matter expert for Veeva, TrackWise, Maximo, and other Quality systems as assigned.
  • Develop and maintain application roadmaps aligned with business priorities, compliance requirements, enterprise architecture, and organizational growth.
  • Own or coordinate system configuration, administration, maintenance, upgrades, integrations, and lifecycle activities for assigned applications.
  • Partner with Quality stakeholders to define business requirements and implement enhancements that improve compliance, efficiency, data visibility, and user experience.
  • Manage vendor relationships, services, licensing considerations, and support agreements for assigned Quality platforms.
  • Establish and maintain governance processes with Quality process owners for system change control, release management, access management, issue resolution, and lifecycle documentation.
  • Lead or coordinate risk-based computerized system validation activities, including requirements, risk assessments, test planning and execution, traceability, and periodic reviews.
  • Maintain assigned systems in a validated state and support compliance with applicable regulatory and quality requirements, including FDA requirements, ISO 13485, 21 CFR Part 11, applicable GxP expectations, and data integrity principles.
  • Maintain inspection- and audit-ready system documentation and support internal audits, external audits, and regulatory inspections as needed.
  • Monitor system performance, usage, security, access, and data integrity, and coordinate timely resolution of identified issues.
  • Analyze Quality processes and identify opportunities for automation, standardization, simplification, and improved controls.
  • Lead cross-functional initiatives involving Quality systems, enterprise platforms, reporting tools, and integrated business processes.
  • Collaborate with technical and business teams to design, implement, and support integrations between Quality systems and ERP, manufacturing, training, asset management, and analytics platforms.
  • Establish and maintain appropriate data governance practices for Quality-related master data, records, interfaces, and reporting.
  • Develop and monitor measures of system effectiveness, adoption, service performance, and process outcomes.
  • Lead system implementations, upgrades, migrations, and optimization projects from requirements through stabilization.
  • Develop and manage project plans, milestones, risks, dependencies, budgets, resources, and stakeholder communications.
  • Coordinate vendors, consultants, business stakeholders, and technical resources to deliver project objectives.
  • Facilitate user acceptance testing, deployment readiness, training, change management, and post-implementation support.
  • Serve as an escalation point for complex application issues and provide guidance to system users, process owners, and support teams.
  • Develop or oversee training materials, work instructions, process documentation, and user support resources.
  • Occasional travel may be required based on business needs.

Desired Qualifications

  • A master's degree or relevant professional certification is preferred.
  • Experience in the medical device, pharmaceutical, biotechnology, or another FDA- or ISO-regulated industry is strongly preferred.

About the Company

Glaukos

Medical devices for glaucoma treatment

Glaukos focuses on ophthalmology by developing and commercializing medical devices and therapies for glaucoma, corneal disorders, and retinal diseases. Its products mainly target surgeons who treat eye conditions, with a core technology in micro invasive glaucoma surgery (MIGS). The company’s MIGS devices, such as the Trabecular Micro Bypass Stent and next-generation iStent, are implanted in the eye to improve outflow of eye fluid and lower intraocular pressure, offering a less invasive option compared with traditional surgeries. Glaukos differentiates itself by pioneering MIGS and bringing the first US-approved MIGS device to market in 2012, continuing to expand its portfolio through research, development, and strategic acquisitions. The company aims to improve patient care by providing safer, effective, and longer-lasting treatment options for glaucoma and related eye diseases, addressing unmet needs in ophthalmology.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Aliso Viejo, CA
Founded
1998

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