Quality Control Leader: Manufacturing & Compliance

IRhythm Technologies Inc.

Aliso Viejo (CA)

On-site

USD 90,000 - 120,000

Full time

4 days ago
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Job summary

iRhythm Technologies seeks a Quality Control Manager to lead inspection and material control across manufacturing and receiving in Orange County. You will direct quality inspectors, develop plans, and ensure regulatory compliance before lot release.

Responsibilities include mentoring teams, reviewing batch records, monitoring quality metrics, and driving continuous improvement on the production floor. The role requires FDA 21 CFR 820 and ISO 13485 knowledge, plus MRB and FAI experience.

Qualifications

  • Experience leading quality inspection or manufacturing teams.
  • Knowledge of FDA 21 CFR 820 and ISO 13485 requirements.
  • Experience with batch record review and documentation control.

Responsibilities

  • Lead, coach, and develop Manufacturing Quality Inspectors and Receiving Inspection personnel.
  • Develop and implement inspection plans, sampling strategies, and control plans with cross-functional partners.
  • Oversee identification, documentation, and containment of nonconforming material and support MRB activities.
  • Review and verify manufacturing batch records and travelers for completeness and regulatory compliance prior to lot release.
  • Monitor quality metrics, conduct Gemba walks, and drive continuous improvement initiatives.

Skills

Leadership
Regulatory knowledge
Batch records review
Nonconformance management
MRB
Receiving inspection
FAI
Inspection plans
Sampling strategies
Control plans

Job description

iRhythm Technologies seeks a Quality Control Manager to lead inspection and material control across manufacturing and receiving in Orange County. You will direct quality inspectors, develop plans, and ensure regulatory compliance before lot release.

Responsibilities include mentoring teams, reviewing batch records, monitoring quality metrics, and driving continuous improvement on the production floor. The role requires FDA 21 CFR 820 and ISO 13485 knowledge, plus MRB and FAI experience.

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