Manufacturing Engineer
Publication date:
06 October 2024Workload:
100%Contract type:
Unlimited employment- Place of work:Portage
Stryker’s Medical manufacturing facility is seeking to hire a Manufacturing Engineers to support sustaining engineering efforts in Portage, Michigan.
WHO WE WANT:
-
Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.
-
Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes – finding ways to simplify, standardize and automate.
-
Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
WHAT YOU WILL DO:
-
As the Manufacturing Engineer, you will collaborate with Quality Engineering to provide manufacturing support.
-
You will be responsible for providing manufacturing engineering support to specific projects including change analysis, risk analysis, and manufacturing readiness.
-
As the Manufacturing Engineer, you will troubleshoot and resolve issues relating to the safety, efficacy, quality, cost, or delivery of components and finished devices.
-
You will conduct qualification, verification, and validation activities to produce medical devices.
-
You will be responsible for completing engineering work and contribute to new product development teams and product support, typically including the following activities: technology development, test of materials or products, preparation of specifications, six sigma, process studies, process improvements, and report preparation.
-
You will design, procure, and fabricate tooling and fixtures.
-
As the Manufacturing Engineer, you will design, document, and improve manufacturing processes and operations that control the safety and efficacy of finished devices.
-
Train, develop, and/or provide work direction to operators and technicians.
-
Participate on cross-functional project teams. Coordinate, manage, and document project work and progress, and recommend appropriate revisions.
-
Participate in design control efforts related to risk analysis (failure mode and effect analysis) & design reviews.
-
You will interface with product builders or extrusion technicians, production supervisors, and engineers in troubleshooting problems on the production floor.
-
Your goal will be to identify and implement process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance.
-
In this role you will design, develop, testing, and validate equipment and processes; analyze and interpret process models and recommend process improvements.
WHAT YOU NEED:
-
Bachelor’s degree in engineering - required
-
Bachelor’s degree in mechanical, industrial or manufacturing engineering - highly preferred
-
Controls, PLC, SQL experience - preferred
-
Manufacturing engineering in a FDA regulated environment - preferred
-
Previous manufacturing experience including validations, process efficiencies, lean manufacturing and manufacturing services experience - preferred
-
Ability to read, understand, engineering drawings on common engineering software - preferred
-
Minitab, or similar, statistical software - preferred