Snr Manufacturing Engineer - Urgently Hiring!

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.

What You Can Expect

The Manufacturing Sr. Engineer II is responsible to drive process improvement and process optimization, equipment lifecycle management, and regulatory compliance, ensuring high production efficiency, quality, and cost-effectiveness. This role is integral in leading process validation, equipment qualification, and continuous improvement initiatives while upholding safety standards. The ideal candidate will collaborate cross-functionally with Operations, Quality, R&D and Supply Chain to implement best practices and cutting-edge manufacturing technologies.

How You'll Create Impact

• Develop, maintain and improve controlled technical documentation (prints, procedures, work instructions, specifications, acceptance tests, commissioning plans, transfer documents, and master plans)
• Deep understanding of manufacturing processes used in medical device production and supporting a wide variety of processing applications such as biomaterial transformations and packaging
• Analyze and improve existing manufacturing processes to enhance efficiency, yield, and cost savings
• Implement lean manufacturing and Six Sigma methodologies to reduce waste and variability
• Collaborate with Product Development teams to transition new products from design to full-scale production
• Lead and manage complex projects with high-impact deliverables, ensuring timely execution
• Lead equipment qualification or process validation projects to maintain compliance and operational excellence
• Identify and resolve complex product and process performance issues
• Hands on approach to selection, installation, troubleshooting, diagnostic and repair of manufacturing equipment
• Design, develop, and implement new manufacturing equipment, fixtures, and tools to enhance production capabilities
• Ensure compliance with ISO 13485, FDA 21 CFR Part 810, GMP and EU MDR standards

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

Expected Compensation Range

$100,000 - $120,000

Travel Expectations

EOE