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Medical Device Design Engineer Jobs in Connecticut

Engineer III, Product Design

Southington, CT · On-site

$131K - $157K/yr

Position Summary The Engineer III, Product Design position in the Vascular Access Product ... As a subject matter expert (SME) in medical device development, this position will drive key ...

Engineer III, Product Design

Southington, CT

$131K - $157K/yr

Position Summary The Engineer III, Product Design position in the Vascular Access Product ... As a subject matter expert (SME) in medical device development, this position will drive key ...

Junior Mechanical Engineer

Shelton, CT · On-site

$63K - $82K/yr

Junior Mechanical Engineer Client is a product development company specializing in innovative ... Previous medical device design experience, handheld and electro-mechanical product design ...

New

Engineer I, Product Design

Southington, CT

$131K - $157K/yr

The primary focus of this role will be supporting the post market development and performing design verification of medical device components and products of varying complexity. The engineer is ...

Engineer I, Product Design

Southington, CT · On-site

$131K - $157K/yr

The primary focus of this role will be supporting the post market development and performing design verification of medical device components and products of varying complexity. The engineer is ...

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Senior Electrical Engineer

Trumbull, CT · On-site

$105K - $137K/yr

Drive medical device Design Control compliance by ensuring that all applicable safety, quality and ... Lead and mentor interns and junior engineers. * Manage and mentor interns * Communicate key ...

The primary focus of this role will be supporting the post market development and performing design verification of medical device components and products of varying complexity. The engineer is ...

The primary focus of this role will be supporting the post market development and performing design verification of medical device components and products of varying complexity. The engineer is ...

Validation Engineer

Guilford, CT · On-site

$60 - $80/hr

The Validation Engineer will have primary responsibilities in planning, designing, developing ... Supports the development of validation plans for medical device design functions (software ...

The Validation Engineer will have primary responsibilities in planning, designing, developing ... Supports the development of validation plans for medical device design functions (software ...

The Validation Engineer will have primary responsibilities in planning, designing, developing ... Supports the development of validation plans for medical device design functions (software ...

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Medical Device Design Engineer information

See Connecticut salary details

$20

$47

$91

How much do medical device design engineer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for medical device design engineer in Connecticut is $47.41, according to ZipRecruiter salary data. Most workers in this role earn between $33.37 and $56.73 per hour, depending on experience, location, and employer.

What does a medical device design engineer do?

A Medical Device Design Engineer is responsible for designing and developing medical devices that improve patient care and meet regulatory standards. They work on creating prototypes, testing designs, and ensuring products are safe, effective, and manufacturable. Their role often involves collaborating with healthcare professionals, regulatory specialists, and manufacturing teams. They also stay up to date with technological advancements and compliance requirements in the medical industry.

What skills and qualifications are needed to thrive as a medical device design engineer?

To thrive as a Medical Device Design Engineer, you need a solid background in biomedical engineering, mechanical engineering, or a related field, with expertise in product development and regulatory compliance. Familiarity with CAD software, prototyping tools, and standards such as ISO 13485 and FDA regulations is typically required. Strong problem-solving abilities, creativity, and effective communication skills set top performers apart in this role. These competencies are crucial for developing innovative, safe, and regulatory-compliant medical devices that improve patient outcomes.

How does a medical device design engineer collaborate with cross-functional teams during product development?

Medical Device Design Engineers regularly work alongside professionals from regulatory, quality assurance, clinical, and manufacturing teams. They participate in design reviews, translate clinical needs into technical requirements, and ensure designs meet safety and compliance standards. Effective communication and teamwork are essential, as engineers must incorporate feedback, address concerns from various stakeholders, and document changes throughout the development lifecycle. This collaborative approach helps ensure the final product is both effective and compliant with industry regulations.

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

AspectMedical Device Design EngineerMechanical Engineer
Required CredentialsBachelor's in biomedical, mechanical engineering, or related; certifications like Certified Biomedical Equipment Technician (CBET) are commonBachelor's in mechanical engineering; optional certifications like Professional Engineer (PE)
Work EnvironmentMedical device companies, healthcare settings, R&D labsManufacturing, automotive, aerospace, R&D labs
Industry UsageDesigning and developing medical devices, ensuring regulatory complianceDesigning mechanical systems across various industries

Medical Device Design Engineers focus on creating and refining medical devices, ensuring they meet health regulations and user needs. Mechanical Engineers have a broader scope, working on mechanical systems in multiple industries. While both roles require engineering fundamentals, Medical Device Design Engineers specialize in healthcare applications and regulatory standards.

Infographic showing various Medical Device Design Engineer job openings in Connecticut as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 14% Part Time, 2% Temporary, and 8% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $98,612 per year, or $47.4 per hour.

Engineer III, Product Design

Southington, CT • On-site

ICU Medical
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

$131K - $157K/yr

Full-time

Posted 21 days ago


ICU Medical rating

7.8

Company rating: 7.8 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

155th of 547 rated manufacturers


Job description


Position Summary
The Engineer III, Product Design position in the Vascular Access Product Engineering team will play a critical role in driving the design, development, and implementation of medical devices. This role involves collaborating closely with cross-functional teams including marketing, commercial, quality, regulatory, and medical groups-to ensure that all product designs meet regulatory standards and customer expectations.
As a subject matter expert (SME) in medical device development, this position will drive key projects of significant complexity while applying sound engineering principles, experimental methods, and analytical techniques. The ideal candidate will bring extensive hands-on experience in medical device design and development, with a strong background in documentation, testing, and risk management.
Essential Duties & Responsibilities
  • Drive Design Control Activities: Work on all aspects of design control, including Requirements Management, Design Outputs, Verification & Validation (V&V), Design History File (DHF), and Risk File management.
  • Drive Product Development: Plan, design, and implement new products and changes to post market products, ensuring compliance with applicable medical device standards.
  • Solve Complex Engineering Challenges: Apply experimental, computational, and analytical methods to address technical challenges and ensure product performance.
  • Develop and Maintain Technical Documentation: Create and maintain product specifications, requirements, architecture, design, and usability documents.
  • Conduct and Oversee Testing: Design and execute exploratory, bench, and V&V testing, developing test protocols and generating comprehensive reports.
  • Collaborate with Cross-Functional Teams: Partner with marketing, quality, and regulatory teams to ensure design requirements align with business objectives and regulatory compliance.
  • Corrective Actions and Preventable Actions: Assist manufacturing operations and quality with the root cause analysis, and the development and implementation of solutions for non-conforming events.
  • Design & Model Devices: Utilize SolidWorks to create and refine device models for various product lines, with a focus on high-volume disposable medical devices.
  • Partner with Suppliers & Customers: Collaborate with customers and suppliers to refine designs and ensure manufacturability, with an emphasis on plastics/polymer engineering and injection molding.

Knowledge & Skills
  • Proven Expertise in Medical Device Design: Extensive hands-on experience developing and improving medical devices, including knowledge of FDA regulations and ISO standards.
  • Proficiency in SolidWorks: Strong capability in 3D modeling and drafting and the design for manufacturability.
  • Material & Manufacturing Knowledge: Deep understanding of medical-grade plastics, injection molding principles, and common joining methods.
  • Analytical & Problem-Solving Skills: Strong ability to apply statistical methods, including Design of Experiments (DOE) and tolerance analysis, to solve complex engineering problems.
  • Strong Communication & Collaboration Skills: Ability to effectively communicate with technical and non-technical stakeholders across departments and with suppliers.
  • Knowledge of Engineering Mechanics & Physics: Solid understanding of the principles underlying mechanical design.
  • Familiarity with Machine Shop Practices: Understanding of basic machining operations.
  • Time Management: Ability to handle multiple priorities and meet key deadlines under pressure through effective time management skills.

Minimum Qualifications, Education & Experience
  • Bachelor of Science (B.S.) degree in Mechanical Engineering or a related field from an accredited institution.
  • Minimum of 4 years of relevant experience in medical device design and development.
  • Must be at least 18 years of age.

Work Environment
  • Primarily operates in a professional office environment with standard office equipment.
  • This role is largely sedentary but may involve occasional visits to labs or manufacturing facilities.
  • Typically requires travel less than 5% of the time.

About Us
ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.
With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.
We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you:
  • Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
  • The industry's broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
  • IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
  • Significant US IV solutions manufacturing and supply capabilities.

ICU Medical EEO Statement:
ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.
If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.
ICU Medical EEO Policy Statement
Know Your Rights: Workplace Discrimination is Illegal Poster
ICU Medical CCPA Notice to Job Applicants

What ICU Medical employees say

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About ICU Medical

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

San Clemente, CA, US

Year founded

1984

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