Why This Role Stands Out
This Quality Management Consultant role offers a fantastic opportunity to drive impactful compliance initiatives and hone your expertise in medical device regulations within a long-term project. You'll thrive here if you possess a strong background in quality systems and a passion for continuous improvement. Apply now to contribute your skills to a reputable company!
Quick Overview
Seniority
Mid Senior
Work mode
On Site
Location
Reedsville, PA, United States
Posted
20 hours ago
ComplianceRoot Cause Analysis
Job Description
Hi ,
Our client is looking for an Quality Management Consultant for Reedsville, PA (Day 1 Onsite) a project and below is the detailed requirement.
Job Title: Quality Management Consultant
Location: Reedsville, PA (Day 1 Onsite)
Duration: Long Term
Responsibilities:
- Bachelor’s degree in Computer Science, Information Systems, Business, or a related field.
- Must Support quality remediation and compliance initiatives by managing nonconformance, CAPA, deviation, complaint handling, and quality system activities. Perform quality assessments, root cause investigations, data analysis, and quality improvement initiatives while ensuring compliance with medical device regulations and standards
- Must have a CAPA Lifecycle Management.
- You should have a Nonconformance and Deviation Management.
- Must have a Root Cause Analysis Techniques.
- Good Experience in 8+ years of Medical Device Quality Systems experience.
- You should have a Minimum 3 years of CAPA management experience.
- Strong Experience supporting regulatory audits and inspections.
- Good Experience in eQMS and Quality Metrics Reporting.
- Must have a FDA 21 CFR Part 820, ISO 13485, ISO 14971.
- Good Experience to Manage CAPA lifecycle from initiation to closure.
- Must Monitor CAPA timelines, aging, and effectiveness.
- You should Facilitate CAPA review meetings and follow-ups.
- Must Review CAPA documentation for compliance.
- Good Experience to Support audit and inspection readiness activities.
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