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Director Engineering Medical Device Jobs in Wisconsin

Schreiber Foods

Director, Engineering

Green Bay, WI · On-site

Project Engineering In this role you will plan, manage and oversee activities of the engineering ... Get access to medical, prescription drug, dental and vision benefits starting day one. This ...

Wisconsin

Senior Medical Device Technician

Kenosha, WI · On-site

$23/hr

Senior Medical Device Technician Job Category: University Staff Employment Type: Regular Job ... There is no direct interaction with customers. Duties include transporting packages from receiving ...

Guided Search Partners

WI · On-site

$120 - $160/hr

... Director to oversee two facilities and help elevate the company's Quality Management System. The ... Degree in Engineering, Life Sciences, or related field preferred. * 10-15+ years in medical device ...

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Director Engineering Medical Device information

What are the typical challenges faced by a director of engineering in the medical device industry?

A Director of Engineering in the medical device field often navigates complex regulatory requirements while balancing innovation and speed-to-market. They frequently manage cross-functional teams, oversee rigorous testing and verification processes, and must ensure that all products meet strict quality and safety standards. Collaboration with regulatory, clinical, and marketing teams is essential to align technical development with business objectives. Additionally, adapting to evolving technology and changes in regulatory landscapes can present ongoing challenges, making strong leadership and adaptability key assets.

What are the key skills and qualifications needed to thrive in the director engineering medical device position?

To excel as a Director Engineering Medical Device, you need extensive experience in engineering management, regulatory compliance (such as FDA and ISO standards), and a background in medical device design or related technical fields. Proficiency with product lifecycle management (PLM) tools, design control systems, and quality management certifications like Six Sigma or PMP are highly valuable. Outstanding leadership, strategic thinking, and the ability to communicate effectively across multidisciplinary teams help set top performers apart. These capabilities are crucial to successfully guide high-stakes projects, ensure regulatory compliance, and drive innovation in a highly regulated industry.

What is a director engineering medical device?

A Director of Engineering in the medical device industry leads the design, development, and testing of medical technologies while ensuring compliance with regulatory standards. They manage engineering teams, oversee project timelines, and collaborate with cross-functional departments, including R&D, quality assurance, and manufacturing. Their role involves strategic planning, resource allocation, and risk management to drive innovation and bring safe, effective medical devices to market.

What are popular job titles related to Director Engineering Medical Device jobs in Wisconsin?

For Director Engineering Medical Device jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Director Engineering Medical Device jobs in Wisconsin look for?

The top searched job categories for Director Engineering Medical Device jobs in Wisconsin are:

What cities in Wisconsin are hiring for Director Engineering Medical Device jobs?

Cities in Wisconsin with the most Director Engineering Medical Device job openings:

Director Engineering Medical Device jobs near you
Infographic showing various Director Engineering Medical Device job openings in Wisconsin as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

Medical Device Quality Inspector

Kellton Tech

Madison, WI • On-site

$30/hr

Contractor

Re-posted 23 days ago

Job description

Job Title: Medical Device Quality Inspector
Location: Madison, WI (Onsite)
Pay Rate: $30/hr. on W2

Job Summary

The Medical Device Quality Inspector is responsible for ensuring that materials, processes, and activities involved in daily device manufacturing, processing, and packaging meet current Good Manufacturing Practices (GMP) and comply with ISO 13485 and applicable quality standards. This position plays a key role in maintaining the quality integrity of medical device products through precise inspection and documentation.

Key Responsibilities

  • Inspect parts according to engineering drawings and specifications.
  • Perform dimensional inspections using precision tools such as calipers, micrometers, gage pins, plug gages, and thread gages.
  • Record acceptance data in the SAP ERP system after inspection.
  • Enter failure data into nonconforming material reports (NCMRs) when applicable.
  • Support daily production activities and collaborate with the team to meet quality and output goals.
  • Follow all established procedures in compliance with FDA and ISO 13485:2008 standards.
  • Maintain documentation in accordance with GMP and company policies.
  • Adapt to various inspection assignments and assist team members as needed.
  • Work overtime when required based on production schedules and incoming part volumes.

Desired Experience

  • Experience with optical measurement machines or a Coordinate Measuring Machine (CMM).
  • Familiarity with ISO 13485 or ISO 9001 quality management systems.
  • Prior experience with material or component inspection in a regulated environment preferred.
  • Exposure to computer-based quality systems; SAP experience is a plus (training provided).

Qualifications

  • Education: High School Diploma or equivalent.
  • Language: Ability to read and write in English.
  • Mathematical Skills: Basic math proficiency required.
  • Technical Skills:
  • Ability to use precision measurement tools such as calipers, micrometers, and thread gages.
  • Proficiency with Microsoft Word and Excel.
  • Soft Skills:
  • Strong attention to detail and defect identification.
  • Ability to work efficiently in a fast-paced team environment with minimal supervision.
  • Flexibility to work overtime as required.

About the Role

This is a hands-on quality inspection position within a team-oriented environment that supports manufacturing operations. The ideal candidate is detail-oriented, computer-proficient, and eager to learn inspection procedures under regulated (FDA and ISO 13485) conditions.