At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
What You Can Expect
Job Summary
Responsible for gathering relevant, factual information and data in order to solve quality related problems. Resolve issues by identifying and applying solutions from acquired technical experience and guided precedents. Plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Work effectively/ productively with all departments by developing a team atmosphere. Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. Mentors less senior staff within the department.
How You'll Create Impact
Principal Duties and Responsibilities
Evaluating process methods and systems to meet performance and quality requirements.
Establishing quality plans for systems and processes for general and specific product performance needs
Monitoring performance of processes to standards
Applying ISO and QSR requirements to processes and procedures for Zimmer and outside suppliers; Working with suppliers on new product introduction to ensure that quality and performance requirements are fulfilled
Assisting Manufacturing, Sourcing and Development in the interpretation and application of regulations
Developing and maintaining department and project budgets
Develop and maintain project plans for system deployments and enhancements
Training and mentoring less experienced team members and cross-functional peers
Identifying and/or developing new technologies
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 OutExpected Areas of Competence
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.Ability to deliver, meet deadlines and have results orientation.Able to communicate both orally and in written form to multiple levels of the company.Understanding of QSR/ISO regulations, design assurance and FMEA. Knowledge of statistics, process control, and process capabilityFull working knowledge of all supporting department needs and capabilities, including the ability to discern when inaccurate information is supplied and offer ideas for how to correct it.Thorough knowledge base of existing Zimmer Biomet products and a basic understanding of competitive products preferredYour Background
Education/Experience Requirements
Required
Bachelor's Degree and 6 years of relevant experience, or Associate's Degree and 8 years of relevant experience, or High School Diploma or Equivalent and 10 years of relevant experienceFamiliarity with Good Manufacturing Practices and QSR/ISO standards required.
Preferred
4+ years’ experience in Engineering focused in one of the following areas, Quality, Quality Assurance, Manufacturing, Development, Regulatory or Compliance4+ years FDA regulated industry experienceTravel Expectationsup to 20%
Salary Expectations:
120-145k
EOE/M/F/Vet/Disability