Quality Specialist

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This range is provided by Cleveland Diagnostics. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$60,000.00/hr - $90,000.00/hr

Title Quality Specialist

Location Onsite-Cleveland Office

Reports To Director of Quality Assurance

Job Overview Participate in activities supporting the successful implementation and maintenance of the quality management system (QMS) in compliance with current ISO
13485, EU IVDR, and 21 CFR 820 requirements. Create, review, and грив manage documentation related to the QMS. Participate in cGMP and quality related activities. Requires excellent attention to detail, critical thinking, risk-based decision making, communication, and a consistent quality-minded approach.

• Supplier Management:
  Support the supplier management process including related activities for qualification, audits, surveys, change control, corrective actions, and the approved supplier list (ASL).
• Internal Audit Program:
  Schedule and perform internal quality audits, assist in the resolution of audit findings, and manage the resulting records and supporting evidence.
• Batch Record Review:
  Perform comprehensive quality review of completed batch records and associated production records.
• Corrective and Preventive Action (CAPA):
  Support identification and resolution of events, perform root cause investigation, determine corrective action plans, and facilitate on time closure.
• Deviations:
  Support identification and resolution of events, perform risk and impact assessment, implement immediate corrections, perform root cause investigation, determine corrective action plans, and facilitate on time closure.
• Documentation:
  Coordinate, manage, and perform quality review of controlled documents and records.
• 3rd Party Audits:
  Participate in QMS audits of Cleveland Diagnostics by regulators, customers, Notified Bodies, or registrars (ISO certification and surveillance audits).
• Nonconforming Product:
  Assist all departments to identify, investigate, document, and resolve nonconformity events.
• Change Control:
  Support the change control process to determine and address the potential risks and impact of changes to product design, materials, processes, systems, equipment, etc. This includes the management of associated records and supporting documentation.
• Training:
  Coordinate initial QMS training for new hires, assist all departments to manage employee training, and coordinate refresher training.
• Complaint Files:
  Support complaint records, perform root cause investigations, and determine corrective action plans.
• Quality Management Review:
  Support information gathering and analysis for the QMS management review process.
• Quality Oversight:
  Perform quality checks of manufacturing activities including label verification, final release inspection, and records review.
• Continuous Improvement:
  Participate in the creation, revision, and implementation of procedures, forms, and work instructions to improve current processes.
• Prepare forägen and participate in QA-related activities.
• All other duties as assigned.

• Interacts frequently with employees across and at all levels within the organization
• Collaboration expected to resolve identified issues and events
• Participatesscss in cross-functional teams
• Does not have direct reports

• Bachelor’s degree in a scientific discipline such as chemistry, biology, or engineering
• ≥ 4 years of experience in a quality role within a US FDA regulated industry such as medical device or pharmaceutical manufacturing
• Working knowledge and experience with Quality Management Systems (QMS) such as 21 CFR 820, ISO
  13485, or EU IVDR
• Working knowledge and experience with current good manufacturing practices (cGMP) and good documentation practices (GDocP)
• Excellent verbal and written communication skills
• Excellent computer proficiency with Microsoft Office products
• General office and HVAC noise environment

Cleveland Diagnostics, Inc., is developing highly efficacious,…