Associate Director - Corporate Quality Compliance (QMS)

What You Can Expect

This position serves as the organization's subject matter expert on global Quality Management System compliance, providing authoritative knowledge and strategic direction across the full scope of applicable regulations, standards, and international frameworks.  This position also leads a team of quality professionals who define, implement, and monitor the global QMS at Zimmer Biomet.

How You'll Create Impact

• Architect and drive the global Quality Management System strategy, including systemic CAPA programs, quality system enhancements, and cross-functional improvement initiatives that strengthen compliance and operational performance across all manufacturing sites, design centers, and distribution centers.
• Direct the development, harmonization, and continuous improvement of corporate quality policies, procedures, and processes to ensure sustained compliance with applicable global regulations, standards, and evolving regulatory expectations.
• Interface with external regulatory bodies — lead strategy for FDA inspections, notified body audits, and other regulatory engagements across the global network, consult on agency communications, and post-inspection commitments.
• Lead quality due diligence for mergers and acquisitions, designing and executing integration strategies that bring newly acquired entities into full alignment with the Zimmer Biomet Quality Management System.
• Represent Zimmer Biomet in a leadership capacity within key industry bodies (e.g., AdvaMed, AAMI), translating emerging standards, regulatory trends, and industry best practices into actionable updates to corporate quality policies and procedures.
• Own and lead the Corporate Management Review and Global Quality Report process end-to-end — through executive presentation and tracking of resulting actions to closure.

What Makes You Stand Out

• Demonstrated knowledge and experience in interpreting and applying regulations and standards for Quality Management Systems that govern design, manufacturing and distribution of products worldwide including but not limited to FDA 21 CFR Part 820 (QMSR), ISO 13485:2016, EU MDR (EU) 2017/745, Canadian Medical Devices Regulations (SOR/98-282), Japan's Pharmaceuticals and Medical Devices Act (PMD Act) and MHLW Ministerial Ordinance No. 169, MDSAP
• Acts in a balanced and ethical manner when dealing in gray areas of regulation. 
• Utilizes leadership and motivational skills sufficient to manage multiple projects and interface with personnel from varied backgrounds and cultures in local and remote locations across all company disciplines and business units.
• Excellent interpersonal skills – Builds and maintains relationships inside and outside the organization.
• Exhibits good business sense, makes sound and timely scientific and business decisions. 
• Able to advocate positions in the face of adversity.
• Excellent oral, writing, and presentation skills.
• Excellent analytical and problem solving skills.
• Computer literacy including Microsoft Office Suite.

Your Background

• Bachelor’s degree in life sciences, technical discipline, or business is required. (Master’s degree is preferred). 
• 7-10 years of experience in a quality, regulatory or quality compliance role is required.  Experience with establishing and/or maintaining quality management systems in a medical device manufacturing organization is strongly preferred.
• Medical Device regulations knowledge and experience required.
• FDA or Notified Body experience required. 
• Audit or ASQ certifications such as RABQSA, CQA, CQE are strongly preferred.

Travel Expectations

• Up to 20%

Expected compensation: $130,000 - $165,000 base salary. Comprehensive bonus also provided.