The Manufacturing Engineer, under general supervision, will maintain, improve, and optimize manufacturing processes in support of the Syringe and Laboratory Products division.
- Responsible for maintaining assembly documentation and production routings.
- Responsible for identifying and executing production improvement projects from concept to implementation; including component design and system design review, under general supervision of management or senior Engineer.
- Responsible for analysis of new products or design concepts for manufacturability and presentation of the analysis with recommendations and possible solutions.
- Responsible for line yield in assigned areas of responsibility.
- Responsible for internal manufacturing quality and external customer experience quality in assigned areas of responsibility.
- Plan and execute testing to assure adequate performance of assembly processes and tooling.
- Responsible for compliance of manufacturing processes to performance, regulatory, and safety standards.
- Responsible for documenting performed tasks including project descriptions, technical specifications, testing data and implementation notes.
- Responsible for the clear presentation of manufacturing-related designs or processes at design review meetings.
- Responsible for troubleshooting production floor issues and implementing corrective actions. This may include tooling or fixture design changes or collaboration with R&D on product design changes.
- Responsible for training manufacturing operators on new or revised manufacturing process instructions or tooling.
- Demonstrate competency with the company’s internal systems (ECO’s, IS, MRP and CAD software etc.).