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Quality Manager Medical Device Jobs (NOW HIRING)

Kellton Tech

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions Assemble and test finished and semi-finished medical devices per established ...

Kellton Tech

Medical Device Quality Inspector

Madison, WI · On-site

$30/hr

Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $30/hr (W2) Job Summary ... Reports to the Quality Control Manager. * Interfaces primarily with manufacturing, engineering, and ...

System One

Medical Device Assembler

Lakewood, NJ · On-site

$16/hr

Notify managers of any broken pieces * Work with quality control team to ensure devices are properly assembled Medical Device Assembler Requirements: * Good hand-eye coordination * Ability to work in ...

Kelly Services

Quality Manager

Brooksville, FL · On-site

$85K - $100K/yr

Quality Manager Location: Brooksville, Florida Work Arrangement: Onsite Employment Type: Direct ... Experience supporting medical-device design transfer and new-product introduction. * Experience ...

Route 92 Medical Inc

Quality Manager

West Jordan, UT · On-site

$130K - $150K/yr

Identify and plan strategic quality initiatives and projects. * Oversee risk management activities ... Associate's degree + 8 yrs of medical device experience * Bachelor's degree + 7 yrs of medical ...

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Quality Manager Medical Device information

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$24K

$86.2K

$158K

How much do quality manager medical device jobs pay per year?

As of Jul 21, 2026, the average yearly pay for quality manager medical device in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.

What does a Quality Manager do in the medical device industry?

A Quality Manager in the medical device industry is responsible for ensuring that products meet all regulatory requirements and quality standards throughout their lifecycle. They develop, implement, and monitor quality management systems, oversee internal and external audits, and work closely with manufacturing, engineering, and regulatory teams to maintain compliance with standards such as ISO 13485 and FDA regulations. Their role is critical to ensuring patient safety and product efficacy by preventing defects and ensuring consistent quality.

What are some common challenges Quality Managers face when ensuring compliance in the medical device industry?

Quality Managers in the medical device industry often encounter challenges such as keeping up with evolving regulatory requirements (like FDA, ISO 13485, and MDR), coordinating cross-functional teams to maintain strict quality standards, and managing documentation for audits. They must also address nonconformities quickly and implement corrective and preventive actions to avoid product recalls. Effective communication and strong attention to detail are essential for navigating these challenges while maintaining product safety and regulatory compliance.

What is the difference between Quality Manager Medical Device vs Quality Engineer Medical Device?

AspectQuality Manager Medical DeviceQuality Engineer Medical Device
Primary FocusOversees quality systems, compliance, and team managementDesigns, develops, and implements quality testing and inspection processes
CertificationsISO 13485, Six Sigma, Lead AuditorISO 13485, Six Sigma, Certified Quality Engineer (CQE)
Work EnvironmentManagement, regulatory compliance, cross-department collaborationProduct testing, process improvement, technical analysis
Industry UsageUsed across organizations to ensure overall quality managementUsed in product development and testing phases

The main difference is that the Quality Manager Medical Device focuses on managing quality systems and compliance at a strategic level, while the Quality Engineer Medical Device concentrates on technical testing and process improvements. Both roles require similar certifications and work within the same industry but serve different functions within quality assurance.

What are the key skills and qualifications needed to thrive as a Quality Manager in the Medical Device industry, and why are they important?

To thrive as a Quality Manager in the Medical Device industry, you need a solid background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and process improvement, often supported by a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), risk management tools (like FMEA), and certifications such as ASQ Certified Quality Auditor (CQA) or Six Sigma are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring cross-functional alignment. These skills and qualifications are crucial to ensure product safety, regulatory compliance, and the overall success of medical device manufacturing and delivery.
More about Quality Manager Medical Device jobs
What cities are hiring for Quality Manager Medical Device jobs? Cities with the most Quality Manager Medical Device job openings:
What are the most commonly searched types of Quality Medical Device jobs? The most popular types of Quality Medical Device jobs are:
What states have the most Quality Manager Medical Device jobs? States with the most job openings for Quality Manager Medical Device jobs include:
What job categories do people searching Quality Manager Medical Device jobs look for? The top searched job categories for Quality Manager Medical Device jobs are:
Quality Manager Medical Device jobs near you
Infographic showing various Quality Manager Medical Device job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, 18% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Medical Device Assembler

Kellton Tech

Madison, WI • On-site

$23 - $24/hr

Other

Re-posted 10 days ago

Job description

Job Title: Medical Device Assembler
Location: 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 diagnosis, repair with limited supervision. Ensure work is completed in compliance with company quality system and medical device regulations.
Essential Functions
Assemble and test finished and semi-finished medical devices per established work instructions
Document and record assembly and testing result activities in electronic record system (SAP) and paper records per work rules, policies, and procedures
Performs top level and sub-assembly diagnosis and repair as required
Responsible for successful completion of all training in a timely fashion.
Maintain an organized and professional work space.
Education / Experience / Skills:
High school /GED diploma required
Experience working in a team-oriented manufacturing environment required
Experience working in a regulated environment preferred ie. Medical device, pharmaceutical industry
Competencies:
Self-directed
Teamwork
Good communication skills
Proficient with computer systems
Critical thinking
Decision making
Quality focused
Organizational Relationship/Scope:
This role will require cross functional relationships with the Materials group as well as the Engineering group as required.
Working Conditions:
Clean, temperature controlled environment.