Overview
On Site
Full Time
Skills
Manufacturing
Marketing intelligence
MI
Forecasting
Reporting
Sales
Continuous improvement
Management
Productivity
Research design
Evaluation
Medical devices
System requirements
Modeling
Budget
Product design
Analytical skill
Optimization
System integration testing
Risk management
Marketing strategy
Dynamics
Product development
Customer facing
Partnership
Collaboration
Regulatory Compliance
Mentorship
Documentation
Research and Development
Science
Electrical engineering
Mechanical engineering
Biomedical engineering
Requirements management
Systems modeling
Programmable logic controller
Systems engineering
SysML
ISO 13485
ISO 9000
Legal
Job Details
Work Flexibility: Onsite
As a Control Systems Engineer at Stryker, you will Lead in the design, development, modification, and evaluation of the manufacturing control systems. You will also translate user needs to design inputs/ specifications and produce architectural-level layouts and platform designs. This role is located in Kalamazoo, MI.
Who we want:
What you will do:
Lead research, design, development, modification, and evaluation of medical device systems
Apply and mentor others on advanced engineering theories, principles, and concepts
Translate user needs to system requirements
Create and modify complex system and test architectures
Allocate and decompose requirements on a multi-disciplinary (electrical, mechanical, software) project using modeling, simulation, budgeting, or mathematical techniques
Lead Concept Phase activities for a small project or collection of features
Lead and guide in correction of complex product design issues
Lead analytical study, including trade studies, sensitivity studies, optimization studies, performance assessments, and design assessments
Lead system integration testing and verification activities
Contribute to Product Risk Management activities, including identification of failures, mitigations, safety requirements, and design for safety
Implement PLC based controls
Business Responsibilities:
Contribute to competitive and market strategy by demonstrating in-depth knowledge of the market, customer dynamics and competitive offerings
Apply strong understanding of clinical procedures to enhance product development
Contribute and execute customer facing activities like voice of customer and customer centric design in partnership with internal and external stakeholders
Med Device Compliance:
Mentor others as a business unit expert on the usage of industry standards, including design requirements and test strategies per applicable regulations
Lead others to create and refine engineering documentation, such as the Design History file and create more progressive technical content
Contribute to R&D procedures and development of industry standards working closely with cross-functional business units
What You Need:
Bachelor of Science in Software, Electrical, Mechanical, Systems, or Biomedical Engineering
6+ years of post grad experience
Experience in developing and optimizing complex systems
Advanced knowledge of Requirements Management Tools and System Modeling Tools
Ability to communicate complex plans and technical information to team members
Preferred Skills / Engineering tools:
PLC programming, Ignition
Experience with SysML and Model-based Systems Engineering
Experience with SysML / MBSE software tools
Knowledge of ISO 13485 and ISO 14971
Travel Percentage: 10%
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.
As a Control Systems Engineer at Stryker, you will Lead in the design, development, modification, and evaluation of the manufacturing control systems. You will also translate user needs to design inputs/ specifications and produce architectural-level layouts and platform designs. This role is located in Kalamazoo, MI.
Who we want:
- Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
- Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
- Self-directed initiators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.
What you will do:
Lead research, design, development, modification, and evaluation of medical device systems
Apply and mentor others on advanced engineering theories, principles, and concepts
Translate user needs to system requirements
Create and modify complex system and test architectures
Allocate and decompose requirements on a multi-disciplinary (electrical, mechanical, software) project using modeling, simulation, budgeting, or mathematical techniques
Lead Concept Phase activities for a small project or collection of features
Lead and guide in correction of complex product design issues
Lead analytical study, including trade studies, sensitivity studies, optimization studies, performance assessments, and design assessments
Lead system integration testing and verification activities
Contribute to Product Risk Management activities, including identification of failures, mitigations, safety requirements, and design for safety
Implement PLC based controls
Business Responsibilities:
Contribute to competitive and market strategy by demonstrating in-depth knowledge of the market, customer dynamics and competitive offerings
Apply strong understanding of clinical procedures to enhance product development
Contribute and execute customer facing activities like voice of customer and customer centric design in partnership with internal and external stakeholders
Med Device Compliance:
Mentor others as a business unit expert on the usage of industry standards, including design requirements and test strategies per applicable regulations
Lead others to create and refine engineering documentation, such as the Design History file and create more progressive technical content
Contribute to R&D procedures and development of industry standards working closely with cross-functional business units
What You Need:
Bachelor of Science in Software, Electrical, Mechanical, Systems, or Biomedical Engineering
6+ years of post grad experience
Experience in developing and optimizing complex systems
Advanced knowledge of Requirements Management Tools and System Modeling Tools
Ability to communicate complex plans and technical information to team members
Preferred Skills / Engineering tools:
PLC programming, Ignition
Experience with SysML and Model-based Systems Engineering
Experience with SysML / MBSE software tools
Knowledge of ISO 13485 and ISO 14971
Travel Percentage: 10%
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.
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