What are the responsibilities and job description for the Lead Quality Assurance Coordinator position at Integra LifeSciences?
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
Performs the essential duties and responsibilities as listed in section below.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law | EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
Integra - Employer Branding from Integra LifeSciences on Vimeo
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
Performs the essential duties and responsibilities as listed in section below.
- Review of production activities including completed forms and batch records against procedure requirements and product specifications for material and product release.
- Review of quality monitoring and testing activities including environmental monitoring and product surveillance.
- Supports QA procedure changes including writing, revising, training and implementation.
- Conducts training for staff at all levels as it relates to quality assurance review and release procedures. Compiles quality metrics for daily/weekly/monthly reporting and reports metrics to site management
- Compiles information for Quality Management Review
- Conducts inspections of materials
- Reviews records for compliance to procedures such as inspection reports, test records, and Device History Records
- Conducts CAPA investigations, proposes corrective and preventative actions, and conducts verification and effectiveness reviews Initiates Nonconforming Material reports, conducts nonconformance investigations, and presents reports/metrics during periodic meetings
- Participates in audits/inspections by customers and regulatory agencies and compiles corrective and preventative action responses
- Other duties may be assigned as necessary
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law | EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
Integra - Employer Branding from Integra LifeSciences on Vimeo