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Quality Manager Medical Device Jobs (NOW HIRING)

MRINetwork Jobs

Quality Assurance Manager

Itasca, IL · On-site

... medical device standards. ● Develop, implement, and maintain quality system processes, including procedures for design control, production, process validation, and post-market activities. ● Lead ...

MRINetwork Jobs

Quality Assurance Manager

Itasca, IL · On-site

... medical device standards. ● Develop, implement, and maintain quality system processes, including procedures for design control, production, process validation, and post-market activities. ● Lead ...

MRINetwork Jobs

Quality Assurance Manager

Itasca, IL · On-site

... medical device standards. ● Develop, implement, and maintain quality system processes, including procedures for design control, production, process validation, and post-market activities. ● Lead ...

Revance

Project Manager, Medical Device

Dallas, TX · Remote

$8.0K - $105K/yr

We are seeking a Project Manager to support the planning and execution of medical device and ... Support regulatory and quality strategies, ensuring compliance with FDA and international ...

Tekhawks LLC

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Software Project Manager (Medical Device) - Remote

Austin, TX · Remote

$45 - $58/hr

Software Project Manager (Medical Device) Location: Remote (Periodic onsite visits required ... o Systems/Hardware o Quality & Regulatory • Translate business needs into clear software ...

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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 Jun 26, 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.
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Quality Manager Medical Device jobs near you
Quality Manager (Medical Device)

Quality Manager (Medical Device)

LaBine and Associates

Fort Myers, FL

Other

Posted 11 days ago

Job description

**Why the Best Quality Manager in Medical Devices Should Apply for This Role**

Imagine being at the helm of quality operations for a leading company in Fort Myers, where your expertise doesn’t just meet expectations but consistently surpasses them. This is a role tailor-made for someone who has dedicated their career to excellence in quality management, particularly in the medical device industry.

You’ve spent years honing your craft, mastering the intricacies of Quality Control, Quality Assurance, and Continuous Improvement. You understand that in the medical device world, quality isn’t just a department—it’s the foundation of trust, safety, and innovation. Now, imagine leading a team where your leadership doesn’t just maintain standards but elevates them, where your insights drive continuous improvement that has a real impact on people’s lives.

This isn’t just another job; it’s an opportunity to shape the future of quality in a company that values your experience and vision. With your background in pharmaceuticals or medical devices, you know the importance of regulatory compliance and the nuances of ISO 9001 standards. Your Six Sigma training and CQA certification have equipped you to tackle challenges head-on, transforming obstacles into opportunities for improvement.

In this role, you won’t just be managing a team—you’ll be inspiring them. Your ability to communicate effectively, whether in English or Spanish, will help you connect with every member of your team, from the shop floor to the executive suite. You’ll be the driving force behind a culture of quality that permeates every level of the organization.

If you’re ready to take the next step in your career, leading quality operations in a dynamic environment where your expertise will be recognized and rewarded, this is the opportunity for you. Apply today and be the leader who sets new standards for quality excellence in the medical device industry.


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About LaBine and Associates

Sourced by ZipRecruiter

LaBine and Associates is a full service talent acquisition firm specializing in executive search for a myriad of industries. Through our partnerships with experienced associates, we can also provide staffing support, expert consultants, and interim executives for your company’s needs. We have deep industry knowledge with understanding in multiple industries. Our specialists include experts in banking/finance, HR/Legal, Technology, Health Care, Life Sciences, Engineering, Energy, Supply Chain, Mining, Agribusiness and manufacturing.

Industry

Professional, scientific, and technical services

Company size

11 - 50 Employees

Headquarters location

San Mateo, CA, US

Year founded

2013

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