Job Description

What you will do:

You will provide manufacturing engineering leadership and lead multiple complex projects for assigned cells within our Mahwah, NJ site. You will work closely with quality assurance, suppliers, advanced operations, and product development on initiatives that drive best practices and support business objectives.

Additional responsibilities:  

• Develop and manage project timelines within a cross-functional team
• Define and implement specific solutions to technical problems, completing the tasks associated with such projects and writing reports that clearly document the results
• Work closely with operations, engineering services and quality to resolve in-house and supplier quality problems using established problem-solving methodologies
• Actively participate and lead teams to support new product and process design and development activities
• Lead and participate in the development and improvement of the manufacturing process for existing and new products
• Review and approve inspection plans, routers and product drawings
• Facilitate quality remediation and gap closure through partnership with cell quality engineers
• Participate in development, review and approval process and equipment validation/qualifications
• Review and approve nonconforming material and system documentation
• Initiate and support NCR's and CAPA initiatives
• Development and management of Packaging Procedures; develop design rules and guidelines considering performance, cost, and reliability
• Create and maintain component specifications for all primary, secondary and tertiary packaging and develop, conduct and analyze the testing of this packaging
• Interfacing with internal product development engineering team to define package design solution; Manage multiple projects to meet established timelines
• Develop an understanding of Stryker package manufacturing processes 
• Identify viable primary packaging options and alternatives, defining technical parameters

Minimum Requirements:

• Bachelor’s degree in engineering required
• 2+ years of operations engineering experience in a manufacturing environment required

Preferred Skills:

• Medical device or highly regulated industry experience
• Must be able to define root cause of different manufacturing equipment such as inspection and packaging equipment
• Demonstrated proficiency in Lean and problem-solving tools, with a high focus on process improvement
• Working knowledge of quality tools such as failure modes effect analysis (FMEA), geometric dimensioning and tolerancing (GD&T), root cause analysis, and Poke-Yoke

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