Senior Audit Program Specialist

Integra LifeSciences

. Coordinate the annual internal audit schedule, approval, and revisions .

Posted 10/14/2026full-timeUnited StatesSenior💰 $81,650 - $112,700 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating internal audits, managing audit logistics, and supporting compliance with FDA QMSR, ISO 13485, and MDSAP standards. Proficient in quality systems, audit reporting, and continuous improvement processes.

Highest-signal resume keywords

Internal Audit CoordinationFDA QMSR ComplianceISO 13485 ExperienceQuality Systems ProficiencyAudit Report Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Audit PlanningAudit ExecutionQuality Management SystemsAudit Metrics PreparationTrackWise Audit Module

Soft Skills

Strong Organization SkillsEffective Communication SkillsCollaboration Skills

Tools & Technologies

Microsoft OfficeAudit Databases

Certifications & Qualifications

Auditor Training Certification

Industry Keywords

FDA Controlled EnvironmentCompliance RolesContinuous ImprovementMatrix Environment

About the role

Key responsibilities & impact

Coordinate the annual internal audit schedule, approval, and revisions
Support audit planning, scope definition, agenda creation, and audit logistics
Facilitate audit execution for onsite and remote audits
Support auditors with drafting audit reports
Manage cross-functional review and approval of audit reports
Track auditee responses and audit action item status
Maintain audit records and databases
Responsible for auditor training and certification maintenance
Prepare audit metrics and dashboards
Support continuous improvement of audit processes including TrackWise audit module
Assist with site-level preparation for external inspections
Perform other related duties as expected

Requirements

What you’ll need

Bachelor’s degree in Engineering, Science, Quality, or related field
A minimum of 5 years of experience in quality or compliance roles OR an advanced degree with 3 years of experience in quality or compliance roles
Experience with FDA QMSR, ISO 13485, MDSAP
Strong organization and communication skills
Proficiency with quality systems and Microsoft Office
Experience in FDA controlled environment
Strong collaboration skills and experience working in a matrix environment
This position could require up to 20% travel

Benefits

Comp & perks

Medical insurance
Dental insurance
Vision insurance
Life insurance
Short- and long-term disability
Business accident insurance
Group legal insurance
Savings plan (401(k))