Senior Supervisor, Inprocess Qa

Abbott

Pleasanton, United States
Base: $90,000.00 – $180,000.00; bonus/equity: not ...
Not specified
Bachelor's degree in engineering or life sciences
Minimum 5 years regulated environment experience
Knowledge of iso 13485 and fda qsr requirements
Abbott is seeking a Senior Supervisor for In-Process Quality Assurance in Pleasanton, CA, to lead a team overseeing quality control in manufacturing operations. The ideal candidate will have a background in quality management within regulated industries and a strong understanding of compliance standards

Job Summary

  • The Senior Supervisor leads a team responsible for overseeing daily in-process quality activities to ensure manufacturing operations meet strict regulatory standards.
  • Employees qualify for comprehensive benefits including free medical coverage, a high employer contribution retirement plan, and tuition reimbursement programs.
  • This role requires close collaboration with Operations and Engineering to resolve quality issues without disrupting production timelines while maintaining audit readiness.

Matching Summary

Match Score: 85

Abbott is seeking a Senior Supervisor for In-Process Quality Assurance in Pleasanton, CA, to lead a team overseeing quality control in manufacturing operations. The ideal candidate will have a background in quality management within regulated industries and a strong understanding of compliance standards.

Salary

Base: $90,000.00 – $180,000.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • Bachelor's degree in Engineering or Life Sciences
  • Minimum 5 years regulated environment experience
  • Knowledge of ISO 13485 and FDA QSR requirements

Nice-to-have

  • Experience with Lean Six Sigma methodologies
  • Prior supervisory experience managing technical staff
  • Familiarity with SPC and PFMEA tools

Key Requirements

  • Bachelor's degree in Engineering, Life Sciences, or related field
  • 5+ years experience in Quality or Manufacturing within regulated industry
  • Demonstrated expertise in root cause analysis and CAPA management

Work Rights

Not specified

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