Senior Audit Program Specialist
Integra LifeSciences · Facility, NJ +3 more
Corporate & BusinessFull-time$82k–$113kCompany career page
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Role summary
Integra LifeSciences seeks a Senior Audit Program Specialist to manage the corporate internal quality audit program across multiple manufacturing facilities. The role coordinates audit scheduling, planning, execution, report generation, and corrective action tracking while ensuring compliance with FDA, ISO, and global regulatory standards.
What they're looking for
- Bachelor's degree in Engineering, Science, Quality, or related field
- Minimum 5 years quality/compliance experience or advanced degree with 3 years experience
- Knowledge of FDA QMSR, ISO 13485, and MDSAP requirements
- Proficiency with quality systems and Microsoft Office applications
- Experience in FDA-regulated manufacturing environments
- Strong organizational and written/verbal communication skills
- Ability to collaborate effectively in matrix organizational structures
What you'll be doing
- Coordinate annual internal audit schedules, approvals, and revisions across facilities
- Support audit planning, scope definition, agenda development, and on-site/remote logistics
- Draft audit reports and facilitate cross-functional review and approval processes
- Track corrective and preventive actions and maintain audit records and databases
- Prepare audit metrics, dashboards, and support external inspection readiness
Privacy & handoff
This role links to Integra LifeSciences's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.