Technical Support Engineer at Zimmer Biomet
Dover, OH 44622
About the Job
Valued Team member: We are glad you are exploring new opportunities within Zimmer Biomet!
What You Can Expect
The purpose of this position is to execute validation and/or qualification of equipment, method, processes following applicable validation standards or regulations. This person will act as a cross-functional, inter-business unit resource and interact with several functional departments including; IT, Manufacturing, Quality, and experts outside Zimmer to implement Technical Support department goals.
How You'll Create Impact
What Makes You Stand Out
Your Background
Travel Expectations
EOE/M/F/Vet/Disability
What You Can Expect
The purpose of this position is to execute validation and/or qualification of equipment, method, processes following applicable validation standards or regulations. This person will act as a cross-functional, inter-business unit resource and interact with several functional departments including; IT, Manufacturing, Quality, and experts outside Zimmer to implement Technical Support department goals.
How You'll Create Impact
- With oversight from supervisor and mentorship by senior peers:
- Execute system validation processes by following procedures, specifications, and standards to company standards
- Collects and analyzes data for software and product evaluation
- Implement appropriate methodologies to ensure validation resources are deployed according to level of risk.
- Implements software issue resolution, mitigation, and corrective/preventative action plans
- Ensures that suppliers and their products are qualified to appropriate standards and regulations
- Enact measures and reviews to ensure systems, once validated, remain in a validated state throughout their life cycle.
- Manage and confront issues as they arise.
- Assist in the execution of validations regarding the development and implementation of the quality assurance and manufacturing projects.
What Makes You Stand Out
- Able to work well with others and interact effectively with all levels, outside contacts and support personnel.
- Able to multitask, meet deadlines and be results oriented.
- Able to communicate both orally and in written form to multiple levels of the company.
- Must have knowledge around Good Manufacturing Practices, specifically within medical device processes, systems, methods, equipment & software validations.
- Capable to lead, review, & apply statistical sampling plans and lean six sigma tools.
- Provides solution to a variety of technical problems of moderate scope and complexity.
- Works under general supervision while following established procedures.
- Frequent use and application of technical standards, principles, theories, concepts and techniques.
Your Background
- B.S. in Engineering with 0 years of experience in an engineering role.
- Minimum of 2-3 years of experience in an engineering role.
- Six Sigma Certification preferred
Travel Expectations
- Up to 5%
- Applicants should be willing to work flexible hours, including evenings & weekends, as needed.
EOE/M/F/Vet/Disability