Specialist, Quality Documentation
Integra LifeSciencesNew Jersey, United States
Posted December 19, 2025
71300 - 97750 USD year
Full Time
About the Company
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
Job Description
Join Integra LifeSciences and be part of creating change and shaping the future of healthcare. Operate in Integra's corporate document control and training systems to transact changes to quality system documents.
Requirements
- Operate in Integra’s corporate document control and training systems
- Support quality system training and management of quality system training requirements in LMS
- Support record retention program (archiving for offsite, electronic signature)
- Execute change orders in alignment with quality system priorities and the global priorities as defined in the CMP and risk prioritization projects
- Support metric and Management Review updates by managing and collecting periodic review data
- Assist in the administration of the corporate document change management system
- Review and manage change records to ensure the information is accurate and complete
- Participate in the development and roll-out of document change management tools
- Promote and provide guidance in Good Documentation Practices
- Collaborate with departments to ensure that all review activities are executed efficiently and effectively
- Support Record Management, Retention and Repository activities and processes
Benefits
- Medical
- Dental
- Vision
- Life insurance
- Short- and long-term disability
- Business accident insurance
- Group legal insurance
- Savings plan (401(k))