Why engineering at Stryker?

At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development.

Need another reason to apply? Check out these 8 reasons to join Stryker's engineering team: https://www.strykercareersblog.com/post/8-reasons-to-join-strykers-engineering-team

• Responsible for coordinating a project team, assigning individual responsibilities, identifying appropriate resources needed, and developing schedules to ensure timely completion of project
• Measure project performance using appropriate tools and techniques in order to monitor the progress of the project, identify and quantify any variances, perform any required corrective actions, and communicate to all stakeholders
• Lead the identification, assessment, monitoring, and closure of project risks throughout the project lifecycle
• Be aware of differing global/technical/product specific labelling standards and requirements.
• Monitors process of any changes in labelling regulations in the US and/or abroad
• Collaborates with subject-matter experts from PD, Regulatory Affairs, Marketing, and Quality to ensure user needs are captured and regulatory requirements are identified and included in final product labelling.
• Represents the division in corporate meetings regarding the corporate global labelling system.
• Understanding of label requirements. Including knowledge of device markings, packaging level label elements for different types of devices and when to use graphical solutions (symbols).
• Authors and executes divisional quality system procedures on label creation, evaluation, and maintenance of labelling systems.
• Produces and maintains medical device labelling and performs labelling verification to ensure all product labelling is complete and compliant to identified standards and regulations.
• Provide solutions to a variety of technical problems of moderate scope and complexity where analysis of situations, strategy for labelling requires a review of variety of factors.
• Will advocate for and influence best practices and continuous improvement.
• Exercises discretion and independent judgment with respect to matters of significance.
• May periodically lead and train new level employees.
• Must be highly engaged with team and success of team goals.
• Support NC/CAPAs efforts (effectivity checks). May be NC owner.
• SME for audit back-room support

• Minimum level degree qualification
• 2 - 4 years of experience
• Technical aptitude for systems and tools and analytical thinking
• Ability to understand labeling systems and how they interact with other business systems, including PLMs and ERPs.
• Proven ability to implement small to medium-scale projects.
• Well organized, able to support multiple projects. Project management skills. Able to meet deadlines.
• Ability to generate and explain detailed schedules and performance objectives.
• Demonstrated experience in presenting to mid-level management.