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Quality Manager Medical Device Jobs in Raleigh, NC

Medical Device Regulations • TG(MD)R: Therapeutic Goods (Medical Devices) Regulations 2002 • ... Being proactive, managing time effectively, and seeking support when needed are critical to meeting ...

We have an exciting opportunity for a Global Quality Manager to join our team. Reporting to the ... Medical, Dental, and Vision Insurance * Life Insurance and Voluntary Benefit Options * Health ...

We have an exciting opportunity for a Global Quality Manager to join our team. Reporting to the ... Medical, Dental, and Vision Insurance * Life Insurance and Voluntary Benefit Options * Health ...

Collaborate with the development team working with medical device suppliers, CDMOs and CMOs. * Manage the training program and documentation. * Manage the QA document management system. Education and ...

Global Quality Manager

Cary, NC · On-site

$125 - $150/hr

We have an exciting opportunity for a Global Quality Manager to join our team. Reporting to the ... Medical, Dental, and Vision Insurance * Life Insurance and Voluntary Benefit Options * Health ...

Sr. Quality Specialist

Durham, NC · On-site

$125 - $150/hr

The role manages key quality activities including audits, supplier and distributor qualification ... Proficient with FDA Medical Device Requirements (CDRH - Center for Devices and Radiological Health)

Quality Engineer - CARY, NC

Cary, NC · On-site

$89K - $122K/yr

Minimum 3 years of experience in Quality Management Systems - 5 to 7 years preferred - within a regulated medical device environment in a global acting company. * Auditor Certification REQUIRED ...

Experience with design controls, risk management and quality processes used in medical device development. Preferred Qualifications: If you have the following characteristics, it would be a plus:

You will understand the complexities of medical device development and manufacturing and excel at ... Develop trusted advisor relationships with engineering, operations, procurement, quality, and ...

Showing results 21-40

Quality Manager Medical Device information

See Raleigh, NC salary details

$21.2K

$76.2K

$139.7K

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

As of Sep 9, 2026, the average yearly pay for quality manager medical device in Raleigh, NC is $76,171.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,900.00 and $120,200.00 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 the key skills and qualifications needed to thrive as a quality manager in the medical device industry?

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.

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 popular job titles related to Quality Manager Medical Device jobs in Raleigh, NC?

For Quality Manager Medical Device jobs in Raleigh, NC, the most frequently searched job titles are:

What cities near Raleigh, NC are hiring for Quality Manager Medical Device jobs?

Cities near Raleigh, NC with the most Quality Manager Medical Device job openings:

Infographic showing various Quality Manager Medical Device job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $83,754 per year, or $40.3 per hour.

Quality Auditor

Morrisville, NC • On-site

Teleflex
Medical Equipment and Supplies Manufacturing • 10K+ employees

Full-time

Re-posted 4 days ago


Teleflex rating

8.3

Company rating: 8.3 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Expected Travel: Up to 50%
Requisition ID: 14037
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ - trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives.
Position Summary
Teleflex is seeking a Quality Auditor to join our Strategic Compliance department. The successful candidate must possess the ability to analyze and assess quality management systems to ensure compliance and conformance to the intent of the applicable regulations and standards. The ability to interpret regulations and standards, be aware of industry best practice and focus on ensuring safe and effective product outcomes is necessary for this position.
This position is based at our Morrisville, NC office.
Principal Responsibilities
• Plan, execute and document internal quality system audits
• Track audit observations and follow up on resolution
• Compile and report audit metrics
• Train and mentor site quality auditors in general quality system auditing practices
• Provide interpretation and consultation to project teams on regulations and standards
• Assist with the development, implementation and maintenance of the corporate auditor training program
• Assist in training of new auditors
• May present educational content and guidance to other functions
• Adhere to and ensure compliance with the Teleflex Code of Ethics, all company policies, rules, and procedures
• Complete other duties and tasks, as assigned
Education / Experience Requirements
• Bachelor's degree in technical field required
• Minimum of 5 years of experience in a quality or regulatory role in the pharmeceutical or medical device industries
• Minimum of 2 years of experience performing internal or supplier audits as the lead auditor
• Fluency in English required
Specialized Skills / Other Requirements
• Understanding and application of quality systems
• Fluency in Spanish, German and/or Czech desired
• In depth understanding and interpretation experience for the following regulations and standards:
Required:
• FDA Title 21 CFR 820 QMSR
• ISO 13485:2016
Desired:
• MHLW No. 169; Ministerial Ordinance
• SOR 98-282; Medical Device Regulations
• TG(MD)R: Therapeutic Goods (Medical Devices) Regulations 2002
• ANVISA RDC 665/2022
• EU MDR 2017/45 European Medical Device Regulations
• Strong communication and interpersonal skills with a broad spectrum of people from varying backgrounds, education and experience.
• Ability to understand technical operations, processes and validation.
• Critical thinking, logic and analytical skills
• Documentation, organization and time management skills
• Technical writing skills
• Ability to operate with limited supervision within defined parameters
INDIVIDUAL CONTRIBUTORS:
• Commitment to Goals - A strong commitment to achieving goals is essential for personal and team success. It requires taking ownership of tasks, staying focused on priorities, and consistently delivering high-quality work. Being proactive, managing time effectively, and seeking support when needed are critical to meeting deadlines and overcoming challenges. By aligning personal efforts with team and organizational objectives, individual contributors play a vital role in driving results and advancing shared goals.
• Continuous Improvement - Continuous improvement means actively seeking ways to enhance your work, skills, and contributions. It's critical to stay curious, embrace feedback, and look for opportunities to streamline processes or solve problems more effectively. Individual contributors should take initiative to learn from experiences, adapt to change, and apply new knowledge to drive better outcomes. By consistently striving to improve, they add value to their team and support the organization's growth and success.
• Culture and Values - Living our culture and values is essential to fostering a positive, collaborative work environment. Individual contributors demonstrate this by treating others with respect, acting with integrity, and contributing to an inclusive and supportive team culture. It's critical to hold oneself accountable, align actions with shared values, and support the broader mission of the organization. By consistently modeling these behaviors, individual contributors help strengthen the workplace culture and positively influence those around them.
TELEFLEX QUALITY BEHAVIORS:
As a member of the QARA team, you play a critical in our mission to improve the health and quality of people's lives. Below are the quality behaviours that we expect all QARA employees to exhibit every day.
Patient Focused
• We prioritize our patients and users in our decision making.
• We understand our products and recognize our actions affect product quality.
• We understand the impact of product quality on user and patient safety.
Accountable
• We show up prepared and if we say we'll do it, we do.
• We learn from mistakes and address them quickly.
• We speak up and take responsibility.
Preventive
• We proactively look for and address things that could go wrong.
• We speak up when we notice poor quality.
• We correct poor quality and prevent recurrence.
Solution Minded
• We bring solutions to identify problems and are open to change.
• We share and implement ideas to continuously improve.
• We evaluate fully and investigate to root cause.
#LI-DR1
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

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