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Skills
Bioengineeringunmatched
Certified Internal Auditor (CIA)unmatched
Communication Skillsunmatched
Computer Skillsunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Cross-Functionalunmatched
Electrical Engineeringunmatched
Environmental Managementunmatched
Environmental Monitoringunmatched
External Auditunmatched
FDA (Food and Drug Administration)unmatched
FDA Requirementsunmatched
GMP (Good Manufacturing Practices)unmatched
ISO (International Organization for Standardization)unmatched
Internal Auditunmatched
Maintain Complianceunmatched
Manufacturing Requirementsunmatched
Mechanical Engineeringunmatched
Microsoft Excelunmatched
Microsoft Officeunmatched
Microsoft PowerPointunmatched
Microsoft Projectunmatched
Microsoft Wordunmatched
Multitaskingunmatched
Presentation/Verbal Skillsunmatched
Problem Solving Skillsunmatched
Project/Program Coordinationunmatched
Quality Assurance Methodologyunmatched
Quality Controlunmatched
Quality Engineeringunmatched
Quality Managementunmatched
Quality Metricsunmatched
Quality System Requirements (QSR)unmatched
Regulationsunmatched
Regulatory Complianceunmatched
Risk Managementunmatched
Root Cause Analysisunmatched
Team Playerunmatched
Vendor/Supplier Evaluationunmatched
Writing Skillsunmatched
Description
The Quality Systems Specialist role is responsible for supporting all areas of the pre-and post-market quality system activities; ensuring that the Quality System complies with FDA, ISO and customer requirements.
Role and Responsibilities:
Employ quality assurance methodologies in support of quality, engineering, manufacturing and regulatory functions
Responsible for the collection and management of environmental monitoring samples
Support Quality Management System processes such as, but not limited to, control of nonconforming product reports, product holds, deviations, etc.
Conduct internal and supplier audits
Assist in Risk Management activities, FMEAs and ensure compliance to standards and regulations
Investigation and management of customer complaints
Participate in the failure investigation of product complaint and CAPA activities
Lead root cause activities for CAPAs and other systems as needed
Trend quality system metric data
Assist in preparation for external inspections/audits
Review for completeness and adequacy of the Design History Files
Assist in Quality Control functions
Other tasks as assigned.
Qualifications:
Minimum of Bachelor''s degree in technical field (i.e. Bioengineering, Electrical Engineering, Mechanical Engineering or other technical field) and minimum of 1 year of experience
Ability to work in a fast paced, collaborative team environment
Ability to handle multiple projects and coordinate cross functional teams
Knowledge of FDA Quality System requirements, ISO 13485 (Quality System) requirements, ISO 14971 (Risk Management) requirements, Good Manufacturing Practices (GMP) and applicable Quality System Standards
Certified internal/lead auditor is a plus
Able to use and demonstrate root cause analysis tools
Excellent verbal and written communication skills
Effective problem-solving skills
Ability to work in a team minded approach to achieve individual and company success
Fluent in computer skills and, at a minimum, the use of Microsoft Office Word, Microsoft Office Excel, Microsoft Office PowerPoint and Microsoft Office Project programs
Numbers & Facts
Location
Scottsdale, AZ
Industry
Medical Devices and Supplies
Company Size
50 to 99 employees
Year Founded
2015
Website
http://www.innovative-health.com
About Company
Innovative Health introduces a targeted, high-impact Cardiology program to realize the largest possible savings from using reprocessed single-use devices. The Innovative Health team consists of the reprocessing pioneers who founded the industry. Innovative Health is the next generation in reprocessing, realizing optimal savings while reducing complexity.