Senior Pharma Manufacturing Engineer - GMP & Tech Transfer

Glaukos Corporation; San Clemente (CA); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Salary and bonus eligibility

Medical/dental/vision insurance

Stock options

401(k) Employer Match

Paid holidays and time off

Job summary

Glaukos Corporation in San Clemente, CA seeks a Senior Engineer I, Pharmaceutical to lead development/pilot, clinical and commercial manufacturing of pharmaceutical/combination products. You will partner with R&D, CMC, QA, and Regulatory to advance protocols, qualification, tech transfers and documentation.

Responsibilities include hands-on manufacturing at internal or CMOs, troubleshooting, organizing campaigns, and ensuring compliance with GMP.

Qualifications

• Bachelor’s degree in Engineering or Science with 5–8 years of direct clinical and/or commercial GMP experience.
• Experience in clean-room GMP/GLP environments (ISO 5–ISO 8).
• Strong combination of technical, business, and project management skills.

Responsibilities

• Manufacture development, pilot, clinical, verification/validation, stability campaigns, and commercial production internally or at CMOs.
• Troubleshoot and perform investigations for processes and equipment.
• Develop project plans with milestones and obtain team/management approval.
• Organize activities and technicians to support campaigns and ensure deliverables are on schedule.
• Ensure pharmaceutical product development, manufacturing regulations, and quality requirements are met.

Skills

GMP experience

Project management

Process development

Cross-functional collaboration

Education

Bachelor’s degree in Engineering or Science

Tools

SolidWorks

Visio

Minitab

JMP

Job description

Glaukos Corporation in San Clemente, CA seeks a Senior Engineer I, Pharmaceutical to lead development/pilot, clinical and commercial manufacturing of pharmaceutical/combination products. You will partner with R&D, CMC, QA, and Regulatory to advance protocols, qualification, tech transfers and documentation.

Responsibilities include hands-on manufacturing at internal or CMOs, troubleshooting, organizing campaigns, and ensuring compliance with GMP.