Quality Control Team Lead – Medical Devices

Nuclein

Austin (TX)

On-site

USD 75,000 - 110,000

Full time

14 days+

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Job summary

Nuclein is seeking a Quality Control Supervisor to lead QC staff and drive compliance with GMP standards in our Austin facility. The role requires planning, executing, and documenting QC activities for medical devices and components, plus training team members in QC methods and record-keeping.

Responsibilities include coordinating QC resources to meet schedules, performing inspections, reviewing records for accuracy, and supporting process improvements and audits as needed.

Qualifications

  • Associate’s degree or higher in a technical discipline or equivalent experience.
  • Minimum 4 years QC work experience; 2+ years in medical device or regulated industry.
  • Previous supervisory experience preferred.
  • Quality certifications such as ASQ CQI/CQT or ASME GD&T preferred.

Responsibilities

  • Supervises, trains, and mentors QC personnel.
  • Coordinates QC resources to meet production schedules.
  • Executes QC testing and inspection for release to production and finished product.
  • Maintains GMP standards and equipment; performs metrology and supplies management.
  • Performs data analysis, records results, and archives quality records.
  • Reviews quality records for completeness and accuracy.
  • Leads work instructions creation/revision and supports test method development.

Skills

Supervision
Quality control
Problem solving
Attention to detail

Education

Associate’s degree or higher in a technical discipline

Tools

Laboratory equipment

Job description

Nuclein is seeking a Quality Control Supervisor to lead QC staff and drive compliance with GMP standards in our Austin facility. The role requires planning, executing, and documenting QC activities for medical devices and components, plus training team members in QC methods and record-keeping.

Responsibilities include coordinating QC resources to meet schedules, performing inspections, reviewing records for accuracy, and supporting process improvements and audits as needed.

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