Quality Systems Sr Specialist

Valued Team member : We are glad you are exploring new opportunities within Zimmer Biomet!

What You Can Expect

Maintain Site Quality programs to ensure compliance to domestic and international medical device regulations.

How You'll Create Impact

• Develop and facilitate Site Management Review Reports and Meetings and Corporate KPI reporting.
• Develop and implement processes, procedures and instruction to sustain and improve the Quality Management System.
• Support Top Management in the development and implementation of quality systems strategies and objectives.
• Oversee and coordinate the communication and release of corporate documents for all sites.
• Develop and support site document control procedures and work instructions.
• Develop and execute process improvements to ensure Site Quality processes meet users' needs and requirements.
• Coordinate project work related to integration of sites and migration to integrated systems.
• Assist and lead audits, both internal and external, to demonstrate compliance with GMP, ISO, CMDR, and MDD regulations.
• Support coordination of field action activities as needed.
• Support Quality investigations.
• Manage and facilitate external standard assessments.
• Support Annual Product Reviews per established procedure(s).

This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.

What Makes You Stand Out

Your Background

Travel Expectations

Up to 15% for internal audit.

Expected Compensation Range

$90,000-$110,000

EOE / M / F / Vet / Disability