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Supervisor, Manufacturing (2nd shift)

Glaukos Corporation

San Clemente (CA)

On-site

USD 70,000 - 90,000

Full time

7 days ago
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Job summary

At Glaukos Corporation, the Supervisor of Manufacturing will oversee critical operations in the production of medical devices. This role will require strong leadership and communication skills to manage a diverse team, ensure adherence to quality standards, and enhance process efficiency for timely delivery. Candidates with extensive experience in a manufacturing environment, particularly in medical devices, are encouraged to apply.

Qualifications

  • 5+ years in controlled manufacturing environment, preferably medical devices.
  • 2+ years in a supervisory role.
  • Proficiency in GMP and SOP processes.

Responsibilities

  • Supervise manufacturing processes and manage daily production schedules.
  • Perform MRP transactions and ensure documentation compliance.
  • Lead training efforts and maintain inventory accuracy.

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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