Supervisor, Manufacturing (2nd shift)

Glaukos; San Clemente (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

Glaukos is seeking a Supervisor for their manufacturing operations on the 2nd shift in San Clemente, CA. The role involves supervising production processes, managing schedules, ensuring compliance, and training a team in a controlled manufacturing environment, especially in the medical device industry. Candidates should possess strong leadership and communication skills, with a focus on quality and process improvement.

Qualifications

• 5+ years of experience in a controlled manufacturing environment.
• At least 2 years in a lead or supervisory role.
• Familiarity with GMP and SOP-driven environments.

Responsibilities

• Supervise all in-house commercial manufacturing processes.
• Manage daily production schedules and coordinate with technicians.
• Ensure documentation compliance by updating SOPs, DHRs, and training records.

Skills

Leadership

Communication

Process Efficiency

Attention to Detail

Education

High School Diploma

Some College Coursework or Technical Training

Tools

MRP Systems (Expandable or equivalent)

Job description

GLAUKOS – SUPERVISOR MANFUCTURING – 2ND SHIFT (San Clemente, CA)

How will you make an impact?

As a key leader on the production floor, you’ll ensure that life-changing medical devices are built to the highest standards—on time and ready for patients who rely on them. By supervising day-to-day manufacturing operations, you will play a crucial role in ensuring operational excellence, maintaining inventory accuracy, and supporting a team of technicians through consistent training and mentorship. Your leadership will help keep our products moving—and our mission thriving.

What will you do?

• Supervise all in-house commercial manufacturing processes, including assembly, coating, final packaging, and product release.
• Manage daily production schedules and coordinate with technicians to ensure on-time completion of jobs.
• Perform and oversee MRP transactions such as job creation, kitting, transfers, and adjustments using Expandable or similar systems.
• Ensure documentation compliance by updating SOPs, DHRs, and training records in accordance with GMP and medical device industry standards.
• Conduct regular inventory accuracy checks and maintain production efficiency through proper job planning and materials flow.
• Lead on-the-job training efforts and ensure team members meet all required certifications and competencies.
• Communicate issues that could impact production timelines or quality to management promptly and effectively.

How will you get here?

• High school diploma required; some college coursework or technical training preferred.
• 5+ years of experience in a controlled manufacturing environment, preferably medical device, with at least 2 years in a lead or supervisory role.
• Proficiency in MRP systems (Expandable or equivalent) and familiarity with GMP and SOP-driven environments.
• Strong hands-on operations experience and an eye for process efficiency and continuous improvement.
• Excellent verbal and written communication skills, with the ability to interface across all levels of the organization.
• Proven leadership skills with the ability to train, guide, and motivate a diverse production team.
• Attention to detail and a commitment to quality, safety, and accountability in every task.

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