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Medical Device Manufacturing Engineer Jobs (NOW HIRING)

The Manufacturing Engineer will provide manufacturing engineering support to manufacturing lines ... Experience with Class III medical device manufacturing. Additional Information Please contact:

Manufacturing Engineer

Minneapolis, MN · On-site

$76K - $98K/yr

This Manufacturing Engineer role focuses on supporting the production of commercial and non ... Hands-on experience in medical device manufacturing, including familiarity with catheter product ...

... in advanced engineering, prototyping, product development, and micro manufacturing, driving ... Management of new and existing medical device programs. Responsibilities include maintaining ...

Instylla, Inc. is a privately held medical device company based in Bedford, MA, focused on ... The Manufacturing Engineering role is central to maintaining and improving the manufacturability ...

Manufacturing Engineer I

Bedford, MA · On-site

$76K - $98K/yr

Instylla, Inc. is a privately held medical device company based in Bedford, MA, focused on ... The Manufacturing Engineering role is central to maintaining and improving the manufacturability ...

Senior Manufacturing Engineer

Hudson, WI · On-site

$78K - $124K/yr

... in advanced engineering, prototyping, product development, and micro manufacturing, driving ... Management of new and existing medical device programs. Responsibilities include maintaining ...

Senior Manufacturing Engineer

Monroe, NC · On-site

$84K - $115K/yr

Senior Manufacturing Engineer * Monroe, NC * Full-Time | Direct Hire * Production Manufacturing ... The ideal candidate will bring deep expertise in injection molding within medical device ...

Manufacturing Engineer (2nd Shift)

Calabasas, CA · On-site

$77K - $99K/yr

Ensure all processes meet ISO 13485 and FDA regulations for medical device manufacturing. * Develop ... Work with Design Engineering to provide feedback on part designs for manufacturability (DFM)

Manufacturing Engineer (2nd Shift)

Calabasas, CA · On-site

$77K - $99K/yr

Ensure all processes meet ISO 13485 and FDA regulations for medical device manufacturing. * Develop ... Work with Design Engineering to provide feedback on part designs for manufacturability (DFM)

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Medical Device Manufacturing Engineer information

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$47.5K

$85.6K

$120K

How much do medical device manufacturing engineer jobs pay per year?

As of Jul 23, 2026, the average yearly pay for medical device manufacturing engineer in the United States is $85,613.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,000.00 and $94,000.00 per year, depending on experience, location, and employer.

What is the difference between Medical Device Manufacturing Engineer vs Quality Assurance Engineer?

AspectMedical Device Manufacturing EngineerQuality Assurance Engineer
CredentialsBachelor's in engineering or related field; certifications like ASQ CQE beneficialBachelor's in engineering, quality assurance, or related; certifications like ASQ CQE or CQA common
Work EnvironmentManufacturing plants, production lines, R&D labsQuality labs, manufacturing sites, regulatory agencies
Industry UsageDesign, develop, and optimize manufacturing processesEnsure product quality, compliance, and process improvements

While both roles work within the medical device industry and require similar credentials, the Medical Device Manufacturing Engineer focuses on manufacturing processes and product development, whereas the Quality Assurance Engineer emphasizes maintaining quality standards and regulatory compliance.

What are the key skills and qualifications needed to thrive as a Medical Device Manufacturing Engineer, and why are they important?

To excel as a Medical Device Manufacturing Engineer, you need a solid background in engineering principles, manufacturing processes, and regulatory compliance, typically supported by a degree in biomedical, mechanical, or industrial engineering. Familiarity with CAD software, Six Sigma/Lean methodologies, and knowledge of FDA or ISO 13485 standards is essential. Strong problem-solving, teamwork, and communication skills help manage cross-functional projects and ensure product quality. These competencies are crucial for developing safe, effective devices in a highly regulated industry where precision and compliance are paramount.

What are some common challenges faced by Medical Device Manufacturing Engineers during product development?

Medical Device Manufacturing Engineers often encounter challenges in balancing strict regulatory compliance with efficient production processes. Adapting to frequent design changes, ensuring high product quality, and validating manufacturing processes are crucial tasks. Additionally, they collaborate closely with cross-functional teams—including quality assurance, R&D, and supply chain—to troubleshoot production issues and implement improvements. Addressing these challenges requires strong problem-solving skills and a keen attention to detail.

What does a Medical Device Manufacturing Engineer do?

A Medical Device Manufacturing Engineer is responsible for designing, developing, and optimizing manufacturing processes for medical devices. They ensure that products are produced efficiently, safely, and in compliance with regulatory standards such as FDA or ISO guidelines. Their work involves collaborating with design teams, troubleshooting production issues, implementing quality control procedures, and continuously improving manufacturing methods to enhance product quality. Ultimately, they play a key role in bringing safe and effective medical devices to market.
More about Medical Device Manufacturing Engineer jobs
What cities are hiring for Medical Device Manufacturing Engineer jobs? Cities with the most Medical Device Manufacturing Engineer job openings:
What states have the most Medical Device Manufacturing Engineer jobs? States with the most job openings for Medical Device Manufacturing Engineer jobs include:
Infographic showing various Medical Device Manufacturing Engineer job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $85,613 per year, or $41.2 per hour.
Manufacturing Engineer

Manufacturing Engineer

Collabera

Columbia Heights, MN

$74K - $95K/yr

Contractor

Posted yesterday


Job description

Company Description

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. 

Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence.

Job Description

The Manufacturing Engineer will provide manufacturing engineering support to manufacturing lines producing Class III long term implantable medical devices. The manufacturing operations involved may include the following:
Silicone Rubber Molding
Crimping
Resistance Welding
Laser Welding
Adhesive application
Cutting/Trimming
Flushing
Curing/Annealing
Inspection and Testing
Position Responsibilities:
Daily interaction with the manufacturing teams providing hands-on support and troubleshooting of manufacturing processes and equipment. Provide detailed engineering analysis and documentation in the management of material disposition, manufacturing process updates, qualification activities, compliance activities, and CAPA's. Work with the calibration and maintenance groups to ensure that equipment maintenance and calibration is completed on time.
Perform Equipment Installation, Mfg Process Characterization, Operational Qualification, and Performance Qualification (IQ/OQ/PQ) activities, as well as Software Validation and Test Method Validation for manufacturing equipment and processes. Generate all related documentation in compliance with internal and external requirements.
Support manufacturing facility transfer and product transfer activities to offshore facilities.
Develop technical solutions to difficult problems, finding solutions that are thorough, practical, and consistent with organization objectives.
Ensure personal understanding of all applicable quality policy and quality system procedural requirements. Complete required training on time.

Qualifications

Basic Qualifications: 
BS in Engineering 
5 years minimum engineering experience in the medical device field 
Experience with manufacturing process qualification (IQ/OQ/PQ), Software Validation, and Test Method Validation 
Experience with the FDA QSR and ISO13485 
Desired/Preferred Qualifications: 
Experience with Class III medical device manufacturing.

Additional Information

Please contact:

Sagar Rathore

630-485-2166

sagar.rathore(@)collabera.com