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Medical Device Manufacturing Engineer Jobs (NOW HIRING)

We are seeking an experienced Manufacturing Process Engineer to support a growing medical device manufacturing operation specializing in silicone component manufacturing . This role is responsible ...

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

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 ...

Manufacturing Engineer

Manchester, NH · On-site

$72K - $93K/yr

Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life ...

Manufacturing Engineer

Manchester, NH · On-site

$72K - $93K/yr

Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life ...

Manufacturing Engineer

Southbridge, MA

$75K - $97K/yr

Searching for a Manufacturing engineer job where your effort actually matters? We're building a ... Medical device manufacturing experience in ISO 13485 and FDA-regulated environments. * Injection ...

New

Manufacturing Engineer

Keene, NH · On-site

$72K - $93K/yr

Our medical device manufacturer seeks a hands-on Manufacturing Engineer to support the manufacturing process and drive improvements. Key responsibilities include equipment validation (IQ/OQ/PQ ...

Manufacturing Engineer II

Sarasota, FL · On-site

$70K - $90K/yr

Minimum 5-7 years of manufacturing engineering experience within a precision machining or medical device manufacturing environment. Required Skills and Abilities: * Strong hands-on experience with:

Manufacturing Engineer II

San Jose, CA · On-site

$85K - $110K/yr

We are seeking a process-oriented and results-driven Manufacturing Engineer to take the technical lead in process development, new product launches, and overall improvements in a medical device and ...

Manufacturing Engineer

Keene, NH · On-site

$72K - $93K/yr

Our medical device manufacturer seeks a hands-on Manufacturing Engineer to support the manufacturing process and drive improvements. Key responsibilities include equipment validation (IQ/OQ/PQ ...

Manufacturing Engineer

Keene, NH · On-site

$72K - $93K/yr

Our medical device manufacturer seeks a hands-on Manufacturing Engineer to support the manufacturing process and drive improvements. Key responsibilities include equipment validation (IQ/OQ/PQ ...

Manufacturing Engineer

Keene, NH

$72K - $93K/yr

Our medical device manufacturer seeks a hands-on Manufacturing Engineer to support the manufacturing process and drive improvements. Key responsibilities include equipment validation (IQ/OQ/PQ ...

Showing results 41-60

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:

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 Process Engineer

Talnt

Woodland, CA

$150K - $160K/yr

Full-time

Posted 9 days ago


Job description

Manufacturing Process Engineer

Woodland, CA | Full-Time | On-Site

About the Role:

We are seeking an experienced Manufacturing Process Engineer to support a growing medical device manufacturing operation specializing in silicone component manufacturing. This role is responsible for developing, validating, optimizing, and sustaining manufacturing processes that support high-quality production while ensuring regulatory compliance and operational efficiency.

The ideal candidate has extensive experience with silicone injection molding, along with a strong background in process validation, medical device manufacturing, and continuous improvement. This position partners closely with Manufacturing, Quality, Engineering, and Operations to improve process capability, reduce variability, and successfully launch new products into production.

Silicone injection molding experience is required for this position.

Responsibilities:
  • Develop, optimize, and validate manufacturing processes for silicone injection molding and other silicone fabrication operations.
  • Lead process development activities from concept through production, including equipment qualification and process validation.
  • Create and execute validation protocols including IQ, OQ, PQ, process challenges, and Design of Experiments (DOE) to establish robust manufacturing processes.
  • Monitor critical process parameters (CPPs) and critical quality attributes (CQAs) to maintain process control and product quality.
  • Troubleshoot molding processes and manufacturing issues to improve yield, reduce scrap, and maximize equipment utilization.
  • Develop and document manufacturing processes, work instructions, SOPs, routers, Bills of Materials (BOMs), and manufacturing documentation through the Quality Management System.
  • Design and implement process improvements that increase manufacturing efficiency, improve product quality, and reduce production costs.
  • Collaborate with Quality Engineering on deviation investigations, root cause analysis, CAPA activities, and validation projects.
  • Support new product introductions by developing manufacturing processes, fixtures, tooling, and assembly methods.
  • Partner with Production to ensure manufacturing processes consistently meet production schedules and customer requirements.
  • Work with tooling vendors, equipment suppliers, and internal engineering teams to implement new equipment and manufacturing technologies.
  • Support equipment qualifications, process transfers, and manufacturing scale-up activities.
  • Train manufacturing personnel on new processes, equipment, and standardized work instructions.
  • Participate in Lean Manufacturing, Six Sigma, and continuous improvement initiatives to improve operational performance.
Qualifications:
  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Chemical Engineering, Biomedical Engineering, or a related technical discipline.
  • Minimum of 8 to 10 years of manufacturing process engineering experience in a production environment.
  • Required experience with silicone injection molding in a manufacturing environment.
  • Experience developing and validating manufacturing processes for silicone medical device components or similar precision molded products.
  • Strong knowledge of process validation, IQ, OQ, PQ, DOE, statistical process control, and manufacturing process qualification.
  • Experience supporting regulated manufacturing environments, preferably medical device manufacturing operating under FDA Quality System Regulations, cGMP, and ISO 13485.
  • Experience with process optimization, troubleshooting, root cause analysis, and corrective actions.
  • Proficiency with SolidWorks, AutoCAD, or similar CAD software.
  • Strong understanding of tooling, fixtures, automation, and manufacturing equipment.
  • Excellent analytical, communication, and project management skills.
Desired Qualifications:
  • Experience with additional silicone manufacturing processes including extrusion, calendaring, compression molding, liquid silicone rubber (LSR) molding, assembly, or secondary manufacturing operations.
  • Previous validation engineering experience within the medical device industry.
  • Experience leading new product introductions and manufacturing transfers.
  • Lean Manufacturing or Six Sigma certification.
  • Experience developing custom fixtures and production tooling.
  • Knowledge of statistical analysis software such as Minitab.
  • Experience mentoring junior engineers and manufacturing personnel.