Base: $90,000.00 – $180,000.00; bonus/equity: not ...
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Bachelor's degree in engineering or life sciences
5 years experience in regulated manufacturing quality
Knowledge of iso 13485 and fda qsr regulations
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Abbott is seeking a Senior Supervisor for In-Process Quality Assurance in Pleasanton, California. The role involves overseeing a team to ensure compliance with internal quality standards and regulatory requirements in a manufacturing environment.
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Job Summary
The role leads a team responsible for overseeing daily in-process quality activities to ensure manufacturing operations meet strict internal and regulatory standards.
Employees benefit from comprehensive perks including free medical coverage options, a high employer contribution retirement plan, and tuition reimbursement programs.
This position requires cross-functional collaboration with Operations and Engineering to resolve quality issues while maintaining production timelines and audit readiness.
Matching Summary
Match Score: 75
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Abbott is seeking a Senior Supervisor for In-Process Quality Assurance in Pleasanton, California. The role involves overseeing a team to ensure compliance with internal quality standards and regulatory requirements in a manufacturing environment.
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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
5 years experience in regulated manufacturing quality
Knowledge of ISO 13485 and FDA QSR regulations
Experience with root cause analysis and CAPA
Ability to supervise teams of inspectors and technicians
Nice-to-have
Experience with Lean Six Sigma methodologies
Familiarity with SPC and control plans
ASQ CQA or CQE professional certification
Background in high-volume medical device production
Key Requirements
Bachelor's degree in Engineering, Life Sciences, or related field
Minimum 5 years of Quality or Manufacturing experience
Working knowledge of FDA QSR (21 CFR 820) and ISO 13485
Demonstrated experience with nonconformance management and CAPA