Associate Project Engineer

Company Name:
1. Develop new products and processes with input from experienced engineers, physicians, marketing and manufacturing adhering to the design control process. Aid in the redesign of existing components/assemblies and processes to improve quality, utilize automated production techniques, optimize process capabilities, and produce better products in a more cost-effective manner.
2. Assist in the verification and validation activities for new and existing products and components.
3. Perform or coordinate the development of new processes, optimize them utilizing tools such as DOE, accomplish their evaluation through process validation, and assist in their implementation with appropriate controls and metrics.
4. Train manufacturing management, operator and set-up personnel to manufacture according to specifications.
5. Coordinate the transfer of parts, assemblies, documentation and processes from prototype stage, through pilot to production. Generate product, process and experimental activity specifications for the Device Master Record as required.
6. Aid the project teams in meeting project objectives, milestones, and target dates. Update and review project progress on an as-required basis by supervisor.
7. Interface with vendors to obtain quotations, purchase components, and debug problems with production parts.
8. Interface with purchasing and marketing to develop vendor supply agreements for components and/or new products.
9. Resolve manufacturing issues and conduct continuous improvement of manufacturing processes through the use of statistical data analysis techniques such as Process Capability Studies, DOE and SPC. Provide uniform solutions for international manufacturing operations.
10. Monitor and respond to feedback concerning products. As needed, support investigation of product complaints to determine cause and implement corrective action.
11. Learn the requirements of and operate in a medical device manufacturing environment.
12. Document all new ideas for products and/or processes using Teleflex's Intellectual Property Engineering Notebook.
13. Design products, equipment, tooling and components by using engineering principles on a Computer Aided Design (CAD) system.
14. Direct the efforts of draftsmen, technicians, tradesmen, and engineering assistants in the development of products, processes, equipment and documentation.
15. Participate in design and technical phase reviews.
16. Support regulatory submissions and clinical trials as required.
17. Ensure projects are developed and documented compliant with Teleflex's Quality System.
18. Adhere to and ensure the compliance of Teleflex's Code of Conduct, all Company policies, rules, procedures, and housekeeping standards.

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