About the role

Seeking aQuality Leadto support quality remediation and compliance initiatives within the medical device industry. The role will manage CAPA, nonconformance, deviations, complaints, quality systems, root cause investigations, and quality improvement activities while ensuring regulatory compliance.
Key Responsibilities: ManageCAPA, Nonconformance, Deviation, and Complaintactivities. Conduct Root Cause Analysis and implement corrective actions. Analyze quality metrics and identify recurring issues/trends. Support quality audits and FDA readiness initiatives. Collaborate with cross-functional teams on quality improvements.
Required Skills: CAPA, Nonconformance, and Deviation Management. Root Cause Analysis:5 Why, Fishbone, FTA .Quality Metrics and Trend Analysis. Knowledge ofFDA 21 CFR Part 820, ISO 13485, and ISO 14971 .Design Controls and Validation Support.
Preferred Qualifications: Bachelor's degree in Engineering or related discipline.8+ years of Medical Device Quality experience .Experience with Class II/III medical devices .Experience supportingFDA, MDSAP, and ISO audits .ClinDCast offers Healthcare IT solutions and consulting services to payers, providers and life sciences organizations enabling them to enhance care delivery to patients.

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JOB OVERVIEW

Experience level

Manager

Location

Brooklyn, NY

Occupation

Quality Control Systems Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

today

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