Quality Sr Engineer II

Responsibilities

• Evaluate process methods and equipment to meet performance and quality requirements.
• Establish quality plans for equipment and processes for general and specific product performance needs.
• Monitor performance of processes to standards.
• Apply ISO and QSR requirements to processes and procedures for Zimmer and outside suppliers.
• Work with suppliers on new product introduction to ensure that quality and performance requirements are fulfilled.
• Aid Manufacturing, Sourcing, and Development in interpreting and applying regulations.
• Develop and maintain department and project budgets.

Requirements

• Bachelor's Degree in Engineering
• Minimum of 5 years of relevant experience
• Preferred certification as a quality engineer (e.g. CQE) or the Reliability Engineer Certification (CRE) from ASQ
• Strong experience in a Quality Engineering role within the medical device industry (5-7 years preferred)

Qualifications

• Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.)
• Facilitates team efforts on quality engineering projects.
• Able to deliver, meet deadlines, and have a results-oriented approach.
• Communicate both orally and in writing to multiple levels of the company.
• Expertise in Microsoft Office Suite.
• Knowledge of blueprint reading, geometric dimensioning and tolerancing, QSR/ISO regulations, design assurance, FMEA, and product testing methods.
• Experience using optical comparators and CMMs.
• Knowledge of statistics, process control, and process capability.
• Thorough knowledge of existing Zimmer products and a basic understanding of competitive products.

Benefits

• Hybrid position, 3 days onsite per week in Warsaw, Indiana.
• Up to 20% travel expected.