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Medical Device Manufacturing Engineer Jobs (NOW HIRING)

Siri InfoSolutions Inc

Manufacturing Engineer

Warsaw, IN · On-site

$70K - $90K/yr

Role : Medical Device Manufacturing Engineer Location: Warsaw, IN Duration: 6+ months Experience Required 4 - 6 years (Prior Zimmer Biomet experience is preferred) Technical/Functional Skills:

VOLT

Medical Device Manufacturing Tech

Seattle, WA · On-site

$27 - $31/hr

Collaborate with engineering and quality assurance teams to implement process improvements and ... in medical device manufacturing or another regulated manufacturing environment with part ...

Propeller Health

Manufacturing Engineer

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)

ResMed, Inc.

Manufacturing Engineer

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)

MatrixCare

Manufacturing Engineer

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)

ResMed

Manufacturing Engineer

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)

Resonetics

Senior Manufacturing Engineer

Hudson, WI · On-site

$78K - $124K/yr

Management of new and existing medical device programs. Responsibilities include maintaining ... Engineering or relevant experience. * Experience in medical device manufacturing environment ...

Collabera

Manufacturing Engineer

Columbia Heights, MN · On-site

$74K - $95K/yr

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

Actalent

Manufacturing Engineer

Minneapolis, MN

$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 ...

Actalent

Manufacturing Engineer

Minneapolis, MN

$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 ...

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Showing results 21-40

All JobsMedical Device Manufacturing Engineer Jobs

Medical Device Manufacturing Engineer information

See salary details

$47.5K

$85.6K

$120K

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

As of Aug 13, 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?

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:

What job categories do people searching Medical Device Manufacturing Engineer jobs look for?

The top searched job categories for Medical Device Manufacturing Engineer jobs are:

Medical Device Manufacturing Engineer jobs near you
Infographic showing various Medical Device Manufacturing Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $85,613 per year, or $41.2 per hour.

Manufacturing Engineer

Siri InfoSolutions Inc

Warsaw, IN • On-site

$70K - $90K/yr

Contractor

Re-posted 17 days ago

Job description

Role : Medical Device Manufacturing Engineer

Location: Warsaw, IN
Duration: 6+ months
Experience Required 4 - 6 years


(Prior Zimmer Biomet experience is preferred)
Technical/Functional Skills:
Experience supporting medical device manufacturing
Process Validations
Specific experience with process characterization, equipment IQ/OQ, process OQ, and PQ
EOL validations including Cleaning, Upgrade and Packaging
Specific experience with Test method Validation and Gage R&R
Experience with root cause analysis and problem-solving for both technical and process issues
Working knowledge of design control and cGMP requirements for medical device manufacturing per FDA QSR and ISO13485-2003Ability to lead and prioritize multiple medium-complexity project assignments and complete work in a timely manner
Good problem-solving skills using quality and statistical tools
BOM & Router creation and update
Ability to read and understand engineering drawings
Knowledge of basic quality tools, risk analysis (PFMEA), statistics (SPC), Critical-to Quality (CTQ) Analysis
Knowledge of Quality System requirements, ISO and FDA requirements
Ability to effectively work within a cross-functional team to complete critical project tasks
Demonstrates good written and verbal communication skills
Experienced with control procedures, such as the Change Management System, Nonconformance Reports, Engineering Specifications, Corrective and Preventive Action (CAPA), and Work Instructions & Proficient with Statistical Process Control concepts
Microsoft Office Suite and Project

Roles & Responsibilities:

Develops and Executes Process Validation Strategies for EOL including Cleaning and Packaging: Creates plans, protocols (IQ, OQ, PQ), and risk assessments to ensure effective processes for medical devices and equipment.
Ensures Regulatory Compliance: Adheres to FDA (21 CFR 820), ISO 13485, and other relevant regulations, participating in audits and maintaining up-to-date knowledge.
Analyzes Data and Reports Findings: Compiles and analyzes validation data, writes comprehensive reports, and identifies trends for process improvement.
Collaborates Cross-Functionally: Works with Manufacturing, Quality Assurance, Engineering, and other teams to implement cleaning strategies, resolve issues, and provide technical support.
Leads continuous improvement initiatives, manages change controls, troubleshoots cleaning problems, and ensures proper documentation and training.
Creating, maintaining, and improving controlled technical documents such as prints, procedures, bills of materials, and routers.
Supporting a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc.
Conducting feasibility study to estimate a product cost and analyze capital equipment, capacity, and capability requirements
Establishing and improving process methods that meet performance and quality requirements
Developing and executing project plans and schedules for work activities
Communicate (written and verbal) direction and project plans with appropriate personnel from other departments.
Evaluating multiple options to select the most appropriate processes and machining methods
Execute equipment qualification or process validation project(s)
Generic Managerial Skills Not Mandatory

Education Minimum B.S. degree from an ABET-accredited school (or global equivalent) in one of the following engineering disciplines, 2-4 years of experience: Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering, Biomedical Engineering Technology, Bioengineering Technology, Aerospace Engineering or Aeronautical Engineering. Medical device, particularly the Orthopedic industry, experience preferred.

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About Siri Infosolutions

Sourced by ZipRecruiter

Our team of experts first gather each and every requirement of yours. Our research and development team then sit around those requirements and come up with a plan. Our implementation team then executes that plan for optimal results. After that our support team remains in constant touch with you during and after the entire process.

Industry

It services

Company size

201 - 500 Employees

Headquarters location

Edison, NJ, US

Year founded

2005

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