Quality Assurance Coordinator

QA Coordinator – West Valley City, Utah

• Coordinate and support the execution of quality control activities across the facility.
• Collaborate with the QA Manager to identify, prioritize, and monitor quality-related tasks and objectives.
• Facilitate execution of assigned quality system processes in accordance with internal procedures and regulatory requirements.
• Provide guidance and training to QC Technicians and other personnel involved in quality processes.
• Support coordination of inspection activities and remain qualified to perform inspections when operational support is required.
• Support the execution and monitoring of environmental monitoring activities and ensure timely review of related data.
• Serve as process owner or coordinator for assigned quality system processes as defined in controlled procedures or standard work documents.
• Support document control activities and act as backup for document control and training coordination functions when required.
• Promote compliance with cleanroom behavior, personal practices, and gowning procedures to ensure contamination control standards are maintained.
• Communicate status of quality activities and escalate issues that may impact timelines, compliance, or quality objectives.
• Support internal, external, and regulatory audits as required.

• 1–5 years of experience in quality inspection or a similar role within medical device, pharmaceutical, or regulated manufacturing.
• Knowledge of ISO, FDA, and QMSR concepts and guidelines.
• Excellent communication, organizational, and interpersonal skills.
• Strong attention to detail and ability to work accurately, follow instructions, schedules, timelines, and handle multiple priorities.
• Ability to utilize multiple gauges and measurement tools for inspection.
• Proficiency with MS Office (Word, Excel) and electronic quality management systems (eQMS).
• High School Diploma or equivalent; higher education considered.

1–5 years of experience in quality inspection or a similar role within the medical device, pharmaceutical, or regulated manufacturing industry. High School Diploma or Equivalent (education and experience combined will be considered).

• Inspection tools such as calipers, optical comparators, pin gauges, micrometers, and visual inspection equipment.
• RODAC plate testing, viable air sampling, and particulate monitoring using calibrated equipment.
• General office equipment such as telephone, printer, scanner, etc.
• Electronic documentation systems for tracking nonconformances and quality data.
• Microsoft Office (Excel, Word, Outlook) and eQMS platforms.

Ability to sit, stand, bend, and move throughout the facility for extended periods. Repetitive use of hands and fingers to operate equipment and perform inspections. Must be capable of using a keyboard for data entry and documentation. Reasonable accommodations may be made in accordance with the ADA.

$20.24 – $27.36 USD hourly. Pay is determined by job-related skills, experience, and education or training.

Integra Life Sciences is an equal opportunity employer, committed to providing equal employment opportunities to all qualified applicants regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status. If you require accommodations during the application process, please contact .