Senior Supplier Quality Engineer II — Global Quality

Glaukos Corporation; Burlington (MA); On-site; USD 110,000 - 140,000; Full time

Job summary

Glaukos Corporation is seeking a Sr. Supplier Quality Engineer II to join the Global Quality team in Burlington, MA. The role focuses on ensuring supplier quality, compliance, and performance across development, manufacturing, and distribution of medical devices and pharmaceuticals.

You will lead audits, drive corrective actions, and collaborate with cross-functional teams to optimize supplier performance and product reliability. Domestic travel up to 50% is required.

Qualifications

• Bachelor’s degree in Engineering or related technical discipline required.
• 8+ years of experience in Supplier Quality/Quality Engineering or related field.
• Experience in medical device/pharma manufacturing environments.

Responsibilities

• Lead supplier qualification, assessment, and performance management activities.
• Conduct supplier audits, assessments, and on-site inspections for regulatory and company requirements.
• Drive supplier corrective actions and continuous improvement initiatives.
• Partner with Operations, Manufacturing, R&D, Regulatory Affairs, and Quality teams to support product quality and reliability.
• Review supplier risk classifications and qualification requirements for new/existing suppliers.
• Develop and maintain quality agreements and supplier quality documentation.
• Analyze supplier performance metrics and implement actions to improve quality and on-time delivery.
• Support QMS improvements and organizational quality initiatives.
• Travel domestically up to 50% to support supplier-related activities.

Skills

Supplier Quality

Quality Engineering

Audits

QMS

Root cause investigations

Regulatory compliance

Cross-functional collaboration

Analytical thinking

Education

Bachelor's degree in Engineering

Job description

Glaukos Corporation is seeking a Sr. Supplier Quality Engineer II to join the Global Quality team in Burlington, MA. The role focuses on ensuring supplier quality, compliance, and performance across development, manufacturing, and distribution of medical devices and pharmaceuticals.

You will lead audits, drive corrective actions, and collaborate with cross-functional teams to optimize supplier performance and product reliability. Domestic travel up to 50% is required.