Work Flexibility: Onsite

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 teamDefine and implement specific solutions to technical problems, completing the tasks associated with such projects and writing reports that clearly document the resultsWork closely with operations, engineering services and quality to resolve in-house and supplier quality problems using established problem-solving methodologiesActively participate and lead teams to support new product and process design and development activitiesLead and participate in the development and improvement of the manufacturing process for existing and new productsReview and approve inspection plans, routers and product drawingsFacilitate quality remediation and gap closure through partnership with cell quality engineersParticipate in development, review and approval process and equipment validation/qualificationsReview and approve nonconforming material and system documentationInitiate and support NCR's and CAPA initiativesDevelopment and management of Packaging Procedures; develop design rules and guidelines considering performance, cost, and reliabilityCreate and maintain component specifications for all primary, secondary and tertiary packaging and develop, conduct and analyze the testing of this packagingInterfacing with internal product development engineering team to define package design solution; Manage multiple projects to meet established timelinesDevelop an understanding of Stryker package manufacturing processes Identify viable primary packaging options and alternatives, defining technical parameters

Minimum Requirements:

Bachelor’s degree in engineering required2+ years of operations engineering experience in a manufacturing environment required

Preferred Skills:

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

Travel Percentage: 0%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.