What are the responsibilities and job description for the Engineering Technician position at Zimmer Biomet Holdings Inc?
What You Can Expect
Supporting various manufacturing and process engineering related tasks and projects at Zimmer Biomet. Perform technical job functions and work with various cross-functional groups to support day-to-day operations and special projects.
How You'll Create Impact
Review and disposition product Non-Conformance Requests within the system requirements.
Support Engineering and Manufacturing teams on process improvements (cost reductions) and tracking of data to support initiatives. Support floor operations as needed.
Support site EtQ investigations (NCR's, IE's, and CAPA's) and ensure timely closure.
Support DHR, system, and ERP research for quality/process investigations.
Develop and propose process improvements from quality investigations and track savings in STAR system (create charters, manage project implementation).
Support Engineering team in validation activities.
Support Site Engineering Change Requests (creation, management, implementation) for all departments.
Support Maintenance department in fixture/tooling upkeep, replacement, development.
Support Remediation team for remediation activities (sample creation, equipment transfer as required, and documentation of activities).
Update controlled technical documents such as prints, bill of materials, machine programs, tools inventories, fixtures, manufacturing materials, routers, and procedures.
Field travel to support projects.
Makes recommendations for and implements process improvements for internal operations.
Collaborates closely among Supply Chain, Quality, and Operations to ensure smooth flow of daily work.
Execute manufacturing operations when needed to ensure smooth flow of daily work.
Participates in cross-functional meetings to ensure department goals and objectives are properly represented.
Support and collaborate with suppliers.
Support and execute process validations.
Ordering and maintain manufacturing tools, supplies and aids technical documents.
Perform duties in compliance with applicable regulations and standards such as FDA Quality System Regulation and ISO (International Organization for Standardization).
Follow all standard operating procedures, written and oral, at all times.
Provide timely updates on tasks progress and day to day activities.
Perform tasks as assigned by direct supervisor or designee.
Other duties as assigned
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
Computer literate with advanced familiarity with MS Excel
Strong written and verbal communication skills
Results oriented with the ability to accomplish work in a team environment
Strong attention to detail
Demonstrated enthusiasm and willingness to learn
Ability to work unsupervised on assigned tasks
Ability to work and meet with Controlled Environment Area (CEA) environment requirements and procedures.
Demonstrated analytical skills, especially in the areas of process improvement, problem solving, and logical thinking
Highly developed organizational skills – able to handle multiple high priority tasks/projects concurrently.
Your Background
Associate’s degree preferred.
5 years or more experience required, preferably in a related field.
Travel Expectations
>10%.
EOE/M/F/Vet/Disability
Salary : $56,000 - $77,000