Nypro, A Jabil Company offers customers the widest array of design, engineering, supply chain and manufacturing services in the industry. With over 40 years of experience, our highly specialized teams meet the complex demands of the Medical Device, Diagnostics, Pharmaceutical and Consumer Health markets to enable the world's leading brands to fulfill their market potential.
Our Mission: To be the World’s Most Capable and Trusted Healthcare Services Company.
Sr Manufacturing Engineer leads and supports the resources for Manufacturing Engineering within the operating Segment to ensure that their areas of responsibility are successfully covered, which includes the following:
Implement workflow procedures to optimize safety, quality and efficiency. Support the research and purchase of new equipment, tooling and fixtures. Support training for the assembly staff. Develop and document operating procedures and work instructions with the focus on continued productivity and quality. Responsible for validated state of equipment and processes. Coordinates ongoing projects and serves as liaison between external parties, systems and operating segments. Reviews status of projects and budgets; maintains schedules and prepares status reports.
Allocates engineering resources to the engineering tasks and develops training plans for the manufacturing engineers working in the operating segment. Elevates issues and seeks for additional resources with the operating and system segments as needed.
For the assigned operating segment, oversees and ensures compliance on all the engineering responsibilities and standard work listed below.
Is responsible for new product introduction and sustaining processes, which include the following:
o Time studies and line balancing (UCL).
o Developing work instructions and supports the training on them.
o Creates and maintain all product documentation, such as BOM’s, drawings and specifications.
o Equipment purchases.
o Supports equipment installation and setup.
o Validation of equipment, tooling, fixtures and process.
Bachelor’s degree in an engineering discipline with 6+ year of experience in engineering positions.
Expert in Medical Industry Validation Protocols
Experience managing projects, timelines and budgets.
Experience in component, equipment and process validations.
Lean manufacturing experience.
Green Belt (preferable)
Experience on medical devices or regulated industry (preferable)
Experience on Electromechanically process
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