Principal Design Engineer Visa Sponsorship Jobs in Wisconsin
Principal design engineer roles in Wisconsin are concentrated in the state's manufacturing and technology corridors, with employers like Rockwell Automation, Johnson Controls, and Generac Power Systems actively hiring senior engineering talent in Milwaukee, Madison, and the Fox Cities. International candidates pursuing visa sponsorship will find Wisconsin's industrial base offers strong demand for experienced design engineers.
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Get Access To All JobsJob Description:
Participate in the New Product Development (NPI) and design changes, Design History File (DHF) and Device Master Record (DMR) reviews meetings and fully understand the design control process and Quality Engineering. Utilize technical training and compliance experience to ensure that company design control projects comply with internal design control procedures in accordance with FDA and ISO requirements.
Roles & Responsibilities:
- A seasoned, experienced professional with a full understanding of design control process; resolves a wide range of issues in creative ways.
- Responsible for assuring projects meet customer expectations, and regulatory requirements.
- Act as a subject matter expert on design control process and Quality Engineering. The Quality Engineering subjects are Risk Management, Test Method Validation (TMV), Statistics, Reliability Engineering, Process Validation (PV).
- Successfully address complex engineering issues where analysis of situations or data requires an in-depth evaluation of variable factors.
- Provide guidance to engineering staff and other personnel, and ensure that design control requirements are being met in an effective manner in order to achieve quality by design, including those for design verification, validation, specification and procedure development, risk management, and design review.
- Provides input to design and manufacturing engineering project DHF deliverables including material specifications, drawings, inspection procedures, and manufacturing procedures, to ensure that the resulting products can be adequately manufactured and tested. Review DHF files for accuracy and completeness and provide guidance on FDA compliance and procedures.
- Review and approve design control related Change Notices (CNs) within the documentation system as applicable.
- Coordinate the Design Assurance activities of other team members and assist staff with complex tasks that may require considerable judgment and initiative.
- Create processes and process improvements to ensure consistent implementation of internal requirements and external regulations and standards.
- Represent the design quality functions for the review and approval of designated design outputs.
- Assist in the development and maintenance of company procedures for design control, change management, risk management, process validation and related areas of the quality management system.
- Represent the design quality assurance department to FDA, ISO and all other auditors.
- Work independently on high visibility new product development projects; including projects involving multiple technologies and design sites.
- Maintain knowledge of current regulatory requirements and standards as they pertain to the development and release of medical devices.
- Provide mentorship and assistance to junior level staff with more complex tasks that require a higher level of understanding of functions, and escalate issues to supervisor/manager for resolution, as necessary.
- Assist with various projects as assigned by a direct supervisor.
- Other duties as assigned.
Requirements
- Bachelor's Degree required; Advanced Degree preferred.
- Bachelor's degree and 8-12+ years of experience or a master's degree and 6+ years of experience preferred.
- Familiar with critical elements of the design history file including risk management, design verification and validation tests and ensuring compliance of these elements to procedural requirements.
- Ability to multi-task and operate within a fast-paced environment.
- Strong organizational and presentation skills required.
- Excellent oral, written, analytical, computer and interpersonal skills.
Job Description:
Participate in the New Product Development (NPI) and design changes, Design History File (DHF) and Device Master Record (DMR) reviews meetings and fully understand the design control process and Quality Engineering. Utilize technical training and compliance experience to ensure that company design control projects comply with internal design control procedures in accordance with FDA and ISO requirements.
Roles & Responsibilities:
- A seasoned, experienced professional with a full understanding of design control process; resolves a wide range of issues in creative ways.
- Responsible for assuring projects meet customer expectations, and regulatory requirements.
- Act as a subject matter expert on design control process and Quality Engineering. The Quality Engineering subjects are Risk Management, Test Method Validation (TMV), Statistics, Reliability Engineering, Process Validation (PV).
- Successfully address complex engineering issues where analysis of situations or data requires an in-depth evaluation of variable factors.
- Provide guidance to engineering staff and other personnel, and ensure that design control requirements are being met in an effective manner in order to achieve quality by design, including those for design verification, validation, specification and procedure development, risk management, and design review.
- Provides input to design and manufacturing engineering project DHF deliverables including material specifications, drawings, inspection procedures, and manufacturing procedures, to ensure that the resulting products can be adequately manufactured and tested. Review DHF files for accuracy and completeness and provide guidance on FDA compliance and procedures.
- Review and approve design control related Change Notices (CNs) within the documentation system as applicable.
- Coordinate the Design Assurance activities of other team members and assist staff with complex tasks that may require considerable judgment and initiative.
- Create processes and process improvements to ensure consistent implementation of internal requirements and external regulations and standards.
- Represent the design quality functions for the review and approval of designated design outputs.
- Assist in the development and maintenance of company procedures for design control, change management, risk management, process validation and related areas of the quality management system.
- Represent the design quality assurance department to FDA, ISO and all other auditors.
- Work independently on high visibility new product development projects; including projects involving multiple technologies and design sites.
- Maintain knowledge of current regulatory requirements and standards as they pertain to the development and release of medical devices.
- Provide mentorship and assistance to junior level staff with more complex tasks that require a higher level of understanding of functions, and escalate issues to supervisor/manager for resolution, as necessary.
- Assist with various projects as assigned by a direct supervisor.
- Other duties as assigned.
Requirements
- Bachelor's Degree required; Advanced Degree preferred.
- Bachelor's degree and 8-12+ years of experience or a master's degree and 6+ years of experience preferred.
- Familiar with critical elements of the design history file including risk management, design verification and validation tests and ensuring compliance of these elements to procedural requirements.
- Ability to multi-task and operate within a fast-paced environment.
- Strong organizational and presentation skills required.
- Excellent oral, written, analytical, computer and interpersonal skills.
Principal Design Engineer Job Roles in Wisconsin
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Search Principal Design Engineer Jobs in WisconsinPrincipal Design Engineer Jobs in Wisconsin: Frequently Asked Questions
Which companies in Wisconsin sponsor visas for principal design engineers?
Wisconsin's largest engineering employers have established sponsorship track records for senior design roles. Rockwell Automation in Milwaukee, Johnson Controls in Glendale, Generac Power Systems in Waukesha, and Oshkosh Corporation in Oshkosh have all filed Labor Condition Applications for engineering positions. Medical device companies in the Milwaukee metro, including Advocate Aurora Health's technology divisions, also sponsor principal-level design engineers.
What visa types realistically apply to principal design engineer roles in Wisconsin?
Principal design engineers most commonly enter on the H-1B visa, which covers specialty occupations requiring a directly related bachelor's degree and is subject to an annual cap and selection process. Canadian and Mexican citizens may qualify for TN visa status under the USMCA Engineer category. E-3 visa applies to Australian nationals in specialty occupations. H-1B1 visa covers Chilean and Singaporean nationals. Employer-sponsored EB-2 or EB-3 green cards are also a path for long-term hires.
How to find principal design engineer visa sponsorship jobs in Wisconsin?
Migrate Mate lists Wisconsin employers with verified sponsorship histories for principal design engineer roles, letting you focus on companies that have already demonstrated willingness to sponsor. Because Wisconsin's engineering market spans manufacturing, energy, and automation sectors across multiple metros, filtering by role and location on Migrate Mate helps identify active sponsors in Milwaukee, Madison, or the Fox Valley before you apply.
Which Wisconsin cities have the most principal design engineer sponsorship jobs?
Milwaukee and its suburbs, particularly Waukesha and Glendale, account for the largest share of principal design engineer sponsorship activity, driven by Rockwell Automation, Johnson Controls, and the broader manufacturing cluster. Madison supports engineering roles tied to university-affiliated technology firms and state government contractors. Green Bay and the Fox Cities corridor, home to paper and packaging manufacturers, also generate consistent demand for senior design engineering talent.
Are there any Wisconsin-specific factors that affect visa sponsorship for principal design engineers?
Wisconsin's manufacturing concentration means many sponsoring employers are mid-size industrial companies rather than large technology firms, so sponsorship processes can vary more by employer than in coastal tech hubs. The University of Wisconsin-Madison pipeline produces engineering graduates who compete for the same senior roles, but international candidates with specialized experience in automation, power systems, or precision manufacturing often fill gaps that local talent cannot. Wisconsin employers sponsoring H-1B workers must meet DOL prevailing wage requirements for the Milwaukee or Madison wage area, depending on job location.
What is the prevailing wage for sponsored principal design engineer jobs in Wisconsin?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.