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Medical Device Manufacturing Engineer Jobs (NOW HIRING)

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)

Manufacturing Engineer

Calabasas, CA

$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

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

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)

Be Seen First

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company. The perfect ...

Be Seen First

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company. The perfect ...

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

Manufacturing Engineer II

Bedford, MA

$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 ...

Sr Medical Device Engineer

San Diego, CA · On-site

$110K - $152K/yr

Design and optimize manufacturing equipment, fixtures, assembly processes, and operating procedures ... for medical device manufacturing. * Manage engineering projects and timelines independently ...

Manufacturing Engineer II

Bedford, MA · On-site

$77K - $110K/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 ...

Manufacturing Engineer II

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 ...

Sr Medical Device Engineer

San Diego, CA · On-site

$110K - $152K/yr

Design and optimize manufacturing equipment, fixtures, assembly processes, and operating procedures ... for medical device manufacturing. * Manage engineering projects and timelines independently ...

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 ...

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 Sep 3, 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 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.

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 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.

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 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $85,613 per year, or $41.2 per hour.

Director Medical Device Manufacturing Operations

Castle Biosciences

Phoenix, AZ • On-site

Full-time

Medical, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! Learn more at www.CastleBiosciences.comCastle Biosciences Inc. is growing, and we are looking to hire a full-time Director Medical Device Manufacturing Operations working from our Phoenix, AZ office location, with a start date on or before October 1, 2026.Why Castle Biosciences?Exceptional Benefits Package:Excellent Annual Salary + 35% Bonus Potential20 Accrued PTO Days Annually + 10 Paid Holidays401K with 100% Company Match up to 6%3 Health Care Plan Options + Company HSA ContributionCompany Stock Grant Upon HireA DAY IN THE LIFE OF the Director Medical Device Manufacturing OperationsWe're building a brand-new medical device manufacturing operation and need an experienced leader to build it from the ground up. This Director-level role will own everything from facility startup and process validation, to team building and day-to-day operations. All within an FDA-regulated environment. It's a high-visibility opportunity for someone who thrives on creating something from scratch and wants to make a real impact at a growing diagnostics company. What you'll do: Lead the startup and commercial launch of Castle's new manufacturing facility; from equipment installation and process validation through first production runs; build and lead the manufacturing team, including hiring managers, supervisors, and technicians, and establishing the training and operational systems they need to succeed; own day-to-day manufacturing performance including safety, quality, delivery, and cost; while driving continuous improvement and ensuring ongoing FDA/ISO compliance.REQUIREMENTSBachelor's degree in Engineering, Life Sciences, Operations Management, or related field; advanced degree (MBA, MS Engineering, or related) preferred10+ years of progressive manufacturing leadership experience in medical device, diagnostics, or biotechnology industries, with at least 5 years in director-level or equivalent rolesProven experience leading manufacturing startup operations, greenfield site launches, or significant facility expansions in FDA-regulated environments (21 CFR 820, ISO 13485, GMP)Strong understanding of process validation (IQ/OQ/PQ), equipment qualification, and manufacturing documentation systems*Please see the full job description at the end of the job ad.SCHEDULEThis is a full-time onsite role in Phoenix, Monday-Friday, with hours that vary based on operational needs, especially during the startup phase.READY TO JOIN OUR BIOTECH TEAM?We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon!Castle Biosciences Awards and Research Developments!WORK AUTHORIZATIONAll candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas.ABOUT CASTLE BIOSCIENCES INC.At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail ReasonableAccommodationsRequest@castlebiosciences.com.This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.** No third-party recruiters, please
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