ZipRecruiter

Log In

1

Medical Device Production Jobs (NOW HIRING)

Kellton Tech

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Madison, WI (Onsite) Pay Rate: $23-24/hr on W2 Summary Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided. Perform assembly ...

Apply Early

Astrix Inc

Medical Device Assembler

Trumbull, CT · On-site

$17.75 - $21.50/hr

Inspect parts and finished products to verify they meet specifications and quality standards ... supervisors Medical Device Assembler Qualifications/Requirements: * High school diploma or ...

SmartTalent

Medical Device Assembler

Redmond, WA · On-site

$23 - $26/hr

... products in compliance with GMP guidelines and training. · Follow all standard operating ... Medical device experience is a plus. Apply today and one of our recruiters will help you get ...

Apply Early

Compunnel, Inc.

Medical Device Assembler

Maple Plain, MN · On-site

$24/hr

The ideal candidate is detail-oriented, highly motivated, and committed to maintaining product ... medical device industry. • Strong manual dexterity and ability to work with small tools and ...

Apply Early

next page

Showing results 1-20

All JobsMedical Device Production Jobs

Medical Device Production information

See salary details

$10

$16

$22

How much do medical device production jobs pay per hour?

As of Jul 1, 2026, the average hourly pay for medical device production in the United States is $16.82, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $18.27 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Production, and why are they important?

To excel in Medical Device Production, you typically need knowledge of manufacturing processes, quality control, and regulatory compliance, often supported by a degree in engineering, life sciences, or a related technical field. Familiarity with industry standards (such as ISO 13485), Good Manufacturing Practices (GMP), and tools like ERP systems is crucial. Attention to detail, teamwork, and problem-solving abilities are vital soft skills for ensuring consistent product quality and meeting strict deadlines. These competencies are essential to maintain product safety, meet regulatory requirements, and support efficient and reliable device manufacturing.

What are some common challenges faced by professionals working in medical device production, and how are they typically addressed?

Professionals in medical device production often encounter challenges such as maintaining strict regulatory compliance, ensuring product quality, and meeting tight production deadlines. Adhering to standards like ISO 13485 and FDA regulations requires meticulous documentation and frequent audits. To address these challenges, companies invest in continuous training, implement robust quality management systems, and encourage cross-functional collaboration between engineering, quality assurance, and production teams. This collaborative approach helps streamline problem-solving and ensures consistent product safety and reliability.

What is medical device production?

Medical device production refers to the process of designing, manufacturing, assembling, and testing equipment or instruments used in the diagnosis, treatment, or monitoring of medical conditions. This field involves strict adherence to regulatory standards and quality control to ensure devices are safe and effective for patient use. Production roles may include operating machinery, inspecting products, maintaining documentation, and collaborating with engineers and regulatory teams. The work environment typically involves cleanrooms and specialized manufacturing facilities to maintain hygiene and product integrity.

What is the difference between Medical Device Production vs Medical Device Assembly?

AspectMedical Device ProductionMedical Device Assembly
CredentialsTypically requires technical certifications or training in manufacturing processesOften requires basic technical skills and assembly training
Work EnvironmentManufacturing plants with machinery and quality control processesAssembly lines or cleanroom environments
Industry UsageUsed broadly across manufacturing and production sectors in medical device companiesFocused on putting together components of medical devices
Job FocusOverseeing entire production processes, quality assurance, and equipment operationAssembling device parts according to specifications

Medical Device Production involves managing the entire manufacturing process, including quality control and equipment operation, often requiring specialized certifications. Medical Device Assembly focuses on putting together device components, typically in assembly line settings. Both roles are essential in the medical device industry but differ in scope and responsibilities.

More about Medical Device Production jobs
What cities are hiring for Medical Device Production jobs? Cities with the most Medical Device Production job openings:
What states have the most Medical Device Production jobs? States with the most job openings for Medical Device Production jobs include:
What job categories do people searching Medical Device Production jobs look for? The top searched job categories for Medical Device Production jobs are:
Medical Device Production jobs near you
Infographic showing various Medical Device Production job openings in the United States as of June 2026, with employment types broken down into 15% Full Time, and 85% Part Time. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $34,996 per year, or $16.8 per hour.
Medical Device Manufacturing Engineer

Medical Device Manufacturing Engineer

PMC Smart Solutions LLC

Shelbyville, IN • On-site

$69K - $89K/yr

Full-time

Posted 13 days ago

PMC Smart Solutions rating

5.8

Company rating: 5.8 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

68th of 79 rated plastic manufacturers

Job description

Job Type
Full-time
Description
  • Do you enjoy building and optimizing manufacturing processes that support high-quality medical device production?
  • Are you energized by solving engineering challenges while developing innovative manufacturing solutions that improve efficiency and quality?
  • Are you looking to join a growing team in the medical manufacturing industry where innovation, collaboration, and continuous improvement directly impact products that save lives?

If yes, PMC SMART Solutions is the place for you!
Who is PMC SMART Solutions?
PMC, as a globally-recognized, award-winning contract manufacturer, provides life-saving medical devices and safety-enhancing automotive components to a broad base of international, market-leading OEMs and Tier One customers.
PMC offers services from design for manufacturability and program management through injection molding, full assembly, packaging and sterilization management, focusing on precise-tolerance, intricate devices and components. For its medical customers, PMC functions under ISO 13485 certification, FDA registration and operates state-of-the-art, certified Class 8 (100,000) clean rooms.
PMC is a certified Women-Owned Business Enterprise, offering a comprehensive range of services while supporting global OEMs' supplier diversity goals.
What would you look forward to in this role?
  • Developing and optimizing manufacturing processes that ensure efficient, high-quality, and cost-effective production of medical devices.
  • Designing tooling, fixtures, and manufacturing workflows that improve production accuracy, repeatability, and operational efficiency.
  • Leading engineering activities that support successful new product launches from development through full production readiness.
  • Partnering cross-functionally with Quality, Operations, customers, and Engineering teams to solve technical challenges and drive project success.
  • Supporting validation activities and regulatory compliance efforts that ensure manufacturing processes meet strict medical industry standards.
  • Playing a critical role in manufacturing products that directly support life-saving medical applications.

What key responsibilities would you assume in this role?
Device Building & Process Optimization
  • Develop and implement manufacturing processes supporting medical device production, including molding, machining, assembly, and post-processing operations.
  • Design and implement custom assembly fixtures, inspection tooling, and manufacturing solutions that improve production accuracy and efficiency.
  • Optimize production workflows to reduce cycle times, improve product yield, and lower overall manufacturing costs.
  • Analyze production data to identify process improvement opportunities and support cost reduction initiatives.
  • Troubleshoot manufacturing challenges, identify root causes, and implement corrective actions that improve operational performance.
  • Support Lean Manufacturing initiatives focused on improving efficiency, reducing waste, and increasing throughput.
  • Evaluate manufacturability of customer device designs to ensure production readiness and efficient manufacturing execution.
  • Provide technical feedback during design reviews to improve manufacturability, assembly performance, and product quality.

Project Launch Support
  • Lead engineering activities supporting projects from initial development through successful product launch and production readiness.
  • Coordinate cross-functional teams including Quality, Operations, customers, and internal stakeholders to align project deliverables and timelines.
  • Facilitate technical meetings that drive project alignment, resolve challenges, and maintain momentum toward successful launch milestones.
  • Support Sales and business development efforts by assisting with cost estimates, manufacturing quotes, and lead time projections for customer proposals.
  • Partner with internal teams to ensure manufacturing readiness before transitioning products into production.

Quality & Validation
  • Develop and execute validation protocols supporting equipment, manufacturing processes, and test methods.
  • Perform validation activities including Test Method Validation (TMV), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
  • Ensure manufacturing processes comply with FDA regulations and applicable medical device industry standards.
  • Support preparation and maintenance of documentation required for customer regulatory submissions and internal quality systems.
  • Collaborate with Quality and Engineering teams to ensure validated manufacturing processes remain scalable, repeatable, and audit-ready.
  • Support ongoing compliance initiatives that reinforce PMC's commitment to quality, safety, and regulatory excellence.

Who will you work side by side to achieve extraordinary results?
  • Quality, Operations, and Engineering teams focused on successful product development and production execution
  • Cross-functional teams supporting new product launches and manufacturing readiness
  • Customers and project stakeholders collaborating on medical device development and production requirements
  • Internal leadership teams focused on innovation, quality, and operational excellence
  • Manufacturing teams committed to producing life-saving products with precision and consistency

Requirements
What is needed to thrive in this role?
  • Strong manufacturing engineering experience supporting process development, production optimization, and product launch activities.
  • Experience developing manufacturing processes involving molding, machining, assembly, and post-processing operations.
  • Experience designing tooling, fixtures, and manufacturing systems that improve efficiency and product quality.
  • Strong troubleshooting and root cause analysis skills with the ability to solve technical manufacturing challenges quickly and effectively.
  • Experience supporting validation activities including IQ, OQ, PQ, and Test Method Validation (TMV).
  • Familiarity with FDA regulations, medical device manufacturing requirements, and regulated quality systems.
  • Experience supporting new product launches and managing engineering deliverables from development through production.
  • Strong project management and cross-functional collaboration skills with the ability to manage multiple priorities simultaneously.
  • Experience with Lean Manufacturing, process improvement methodologies, and continuous improvement initiatives.
  • Strong communication skills and the ability to work effectively with customers, internal stakeholders, and cross-functional teams.
  • A proactive mindset focused on innovation, quality, accountability, and PMC's mission of manufacturing products that save lives.

Apply