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Contract Medical Device Design Jobs in Wisconsin

WI · On-site

$98 - $153/hr

... medical device quality, compliance, and safety throughout the product lifecycle, from product ... Design controls, including application of design controls for manufacturing and design changes.

WI · On-site

$91.62 - $152.70/hr

The role requires extensive integrated knowledge of assigned products to support medical device ... Design controls, including application of design controls for manufacturing and design changes.

Design and execute manual test cases and scenarios for invasive cardiology medical devices ... Immediate start with potential for contract-to-hire conversion * Onsite work environment in ...

POSITION SUMMARY The Design Quality Assurance Manager provides quality leadership and oversight for medical device design and development activities to ensure compliance with applicable regulatory ...

Medical device design experience * Experience mentoring junior engineers Why Work With MPE? * Medical, dental, vision, short- and long-term disability, and life insurance starting the first of the ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

Mechanical Design Engineer III

Milwaukee, WI · On-site

$78K - $106K/yr

Five plus years' experience in medical device design * Strong computer, math and oral/written communication skills and attention to detail required * Ability to create / read drawings * Understand ...

Senior Sustaining Engineer - Electrical

Madison, WI · On-site

$108K - $141K/yr

Strong understanding of cGMP, ISO 13485, and regulated medical device environments * Experience with CAPA, complaint investigations, audits, and design documentation * Knowledge of risk management ...

Manufacturing Engineer

Milwaukee, WI · On-site

$71K - $92K/yr

Contract with outside services firms for machine installation and setup. Recommend and document ... Understanding of DFM, medical device design control / quality systems and the product development ...

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Contract Medical Device Design information

What is the difference between Contract Medical Device Design vs Medical Device Design Engineer?

AspectContract Medical Device DesignMedical Device Design Engineer
CredentialsTypically requires a degree in engineering or related field; certifications like ISO 13485 are a plusRequires a degree in biomedical, mechanical, or electrical engineering; professional certifications may enhance prospects
Work EnvironmentProject-based, often freelance or consulting; varies by client and project scopeFull-time employment within a company or R&D department
Employer & Industry UsageUsed by consulting firms, contract agencies, and medical device startupsEmployed by medical device companies, hospitals, or research institutions

Contract Medical Device Design professionals focus on project-specific work, often freelance, while Medical Device Design Engineers are typically employed full-time within organizations. Both roles require similar technical credentials but differ in work setting and employment structure.

What are the most commonly searched types of Medical Device Design jobs in Wisconsin?

The most popular types of Medical Device Design jobs in Wisconsin are:

What are popular job titles related to Contract Medical Device Design jobs in Wisconsin?

For Contract Medical Device Design jobs in Wisconsin, the most frequently searched job titles are:

What cities in Wisconsin are hiring for Contract Medical Device Design jobs?

Cities in Wisconsin with the most Contract Medical Device Design job openings:

Engineer, Device Engineering

Scorpion Therapeutics

Madison, WI • On-site

$120 - $145/hr

Other

Posted 4 days ago


Job description

Responsibilities:
  • Develop and execute strategies/roadmaps for drug-device combination product programs.
  • Provide technical leadership from concept through commercialization and lifecycle management.
  • Lead human factors/usability engineering; author/review plans, URRAs, protocols, reports, and design control documentation.
  • Lead formative/summative human factors evaluations and interpret results.
  • Provide technical expertise in drug delivery technologies, device/system engineering, design controls, risk management, materials, and manufacturing processes.
  • Lead development of prefilled syringes, autoinjectors, and other drug delivery systems.
  • Collaborate cross-functionally (Product Development, Packaging, Manufacturing, Clinical, Supply Chain, Commercial, Quality, Regulatory).
  • Oversee external testing labs; establish/maintain design control processes and DHF documentation.
  • Support design transfer (risk assessments, specs, control strategies, statistical evaluation).
  • Author/review combination-product regulatory submission sections (IND/IMPD/BLA/MAA).
  • Ensure compliance with FDA/EU requirements and standards (ISO 14971, ISO 13485, EU MDR); manage risks and vendors.
Requirements:
  • BS in Biomedical/Mechanical Engineering, Pharmaceutical Sciences, or related.
  • 8+ years in combination product/medical device development; concept-to-commercialization/lifecycle.
  • Experience commercializing prefilled syringes and autoinjectors.
  • Knowledge of subcutaneous delivery systems, device design, systems engineering, materials, manufacturing.
  • Experience with design controls, risk management, human factors/usability engineering.
  • Knowledge of FDA/EU regulations/quality systems (ISO 14971, ISO 13485, EU MDR).
  • Experience with device characterization/design verification testing and device regulatory submission content.
  • Strong communication, cross-functional influence, and project management.
Preferred:
  • Advanced degree.
  • Experience with biological drug products/primary packaging.
  • cGMP process development, manufacturing controls, process risk assessments, design transfer.
  • Fast-paced biotech/pharma experience; mentoring/technical leadership.
Compensation/Benefits:
  • Wisconsin pay range: $120,000–$145,000; California pay range: $135,000–$155,000.
  • Competitive salaries and an excellent benefit package.
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