Senior Project Manager – Global Supplier Quality Systems

Integra LifeSciences

Sr. Project Manager leading and executing global Supplier Quality systems initiatives.

Posted 5/10/2026full-timePrinceton • Massachusetts, New Jersey • 🇺🇸 United StatesSenior💰 $81,650 - $112,700 per yearWebsite

Tech Stack

Tools & technologies

PMP

About the role

Key responsibilities & impact

Lead and manage global Supplier Quality projects, ensuring structured planning, execution, tracking, and on-time delivery of key initiatives.
Drive digital transformation initiatives, including implementation and optimization of eQMS tools supporting Supplier Quality processes.
Partner with site value streams to ensure alignment of Supplier Quality initiatives with operational priorities and business needs.
Track and report on KPIs and project performance metrics, enabling data-driven decisions and continuous improvement.
Coordinate cross-functional teams (Quality, Regulatory, Operations, IT, Procurement) to align priorities, resources, and project outcomes.
Develop and maintain project plans, timelines, risk registers, and stakeholder communication to ensure transparency and accountability.
Support deployment of standardized processes, tools, and reporting frameworks across global Supplier Quality.
Facilitate governance routines (project reviews, status updates, escalation management) to drive execution discipline.
Support integration of acquisitions and new initiatives into existing Supplier Quality systems and frameworks.
Ensure projects and systems align with applicable regulatory and compliance requirements (e.g., FDA, ISO 13485, 21 CFR Part 11).
Promote a culture of accountability, continuous improvement, and strong stakeholder engagement across all projects.

Requirements

What you’ll need

Bachelor degree with 5+ years of experience or equivalent education and years of experience
Master degree with 3+ years of experience or equivalent education and years of experience
Experience leading cross-functional projects.
Strong experience leading deployment of eQMS software solutions.
Strong collaboration skills and experience working in a matrix environment.
Ability to read and understand technical and statistical documents.
Ability to interface with technical and non-technical personnel.
Knowledge of current Good Manufacturing Practices (cGMP) and other applicable standards.
Experience using analytical tools to drive data-based decision making.
PMP Certification Preferred.
Experience with medical products and with ISO and FDA quality systems regulations and medical device design and development cycles is preferred.
Strong knowledge of Power BI, MS Office and eQMS tools and systems.

Benefits

Comp & perks

medical
dental
vision
life insurance
short- and long-term disability
business accident insurance
group legal insurance
savings plan (401(k))

ATS Keywords

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Hard Skills & Tools

Supplier Quality managementeQMS software solutionsdata analysisproject managementrisk managementKPI trackingcontinuous improvementregulatory complianceGood Manufacturing Practicesstatistical analysis

Soft Skills

collaborationleadershipcommunicationstakeholder engagementcross-functional team coordinationaccountabilityproblem-solvingadaptabilitystrategic planningexecution discipline

Certifications

PMP Certification