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Medical Device Quality Assurance Jobs in Raleigh, NC

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

Ensure compliance with relevant FDA, ISO, EU MDR, global, and GSK requirements for medical devices ... Act as site Subject Matter Expert (SME) for device quality processes, providing guidance to ...

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

Ensure compliance with relevant FDA, ISO, EU MDR, global, and GSK requirements for medical devices ... Act as site Subject Matter Expert (SME) for device quality processes, providing guidance to ...

The QA Specialist will perform quality inspections, in-process controls, and finished product ... Perform incoming, in-process, and final inspections of medical device components and finished ...

Quality activities for medical device manufacturing and Design & Development activities throughout all stages of the device development process (e.g. general Product Development / Design Control ...

Quality activities for medical device manufacturing and Design & Development activities throughout all stages of the device development process (e.g. general Product Development / Design Control ...

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 ...

Clinical Trial Quality Assurance Associate * Assist Auditors with Sponsor audits and regulatory ... and medical device firms. For more information, visit www.ctifacts.com Why CTI? * Advance Your ...

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Medical Device Quality Assurance information

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How much do medical device quality assurance jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for medical device quality assurance in Raleigh, NC is $28.47, according to ZipRecruiter salary data. Most workers in this role earn between $18.22 and $33.41 per hour, depending on experience, location, and employer.

What is a medical device quality assurance?

A Medical Device Quality Assurance (QA) job ensures that medical devices meet regulatory standards, quality requirements, and safety guidelines before they reach the market. QA professionals develop and implement quality systems, conduct audits, review documentation, and collaborate with regulatory bodies to maintain compliance with standards like ISO 13485 and FDA regulations. Their role is crucial in preventing defects, ensuring patient safety, and improving product reliability.

What does a medical device quality assurance do?

Professionals in Medical Device Quality Assurance typically review and update quality management systems, conduct internal audits, oversee corrective and preventive action (CAPA) processes, and collaborate closely with product development and manufacturing teams to ensure regulatory compliance. They are often involved in the review of documentation, facilitation of risk assessments, and addressing nonconformances that arise during production or post-market surveillance. Daily work may also include preparing for and participating in regulatory inspections, training staff on quality procedures, and maintaining up-to-date knowledge of relevant standards. This role is both detail-oriented and collaborative, playing a vital part in ensuring product quality and regulatory adherence.

What are the key skills and qualifications needed to thrive in medical device quality assurance?

To thrive as a Medical Device Quality Assurance professional, you need a strong background in quality systems, regulatory compliance, and risk management, often supported by a science or engineering degree and relevant work experience. Familiarity with ISO 13485, FDA 21 CFR Part 820, CAPA systems, and quality management software is typically required, along with certifications such as ASQ Certified Quality Auditor (CQA) being advantageous. Exceptional attention to detail, strong analytical thinking, and effective communication help distinguish top performers in this field. Mastery of these skills and tools ensures that medical devices consistently meet strict regulatory standards, supporting patient safety and organizational reputation.

What are the most commonly searched types of Medical Device Quality Assurance jobs in Raleigh, NC?

The most popular types of Medical Device Quality Assurance jobs in Raleigh, NC are:

What are popular job titles related to Medical Device Quality Assurance jobs in Raleigh, NC?

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

What job categories do people searching Medical Device Quality Assurance jobs in Raleigh, NC look for?

The top searched job categories for Medical Device Quality Assurance jobs in Raleigh, NC are:

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

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

Infographic showing various Medical Device Quality Assurance job openings in Raleigh, NC as of August 2026, with employment types broken down into 64% Full Time, 9% Part Time, and 27% Contract. Highlights an 100% In-person job distribution, with an average salary of $59,224 per year, or $28.5 per hour.

Quality Engineer 1, Product Quality Assurance

Teleflex

Morrisville, NC • On-site

$67K - $87K/yr

Full-time

Posted 9 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 10%
Requisition ID: 14331
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 Engineer 1 to join our team! This role supports the Product Quality Assurance team analyzing post-market data and potential product quality issues for commercialized devices. Accountable for a broad range of technical assignments in the Quality Assurance area under general supervision and working with cross-functional investigation teams. Understands the fundamentals of root cause investigation, risk management, and medical device Quality Management Systems per 21 CFR 820, ISO 13485 and 14971.
Principal Responsibilities
• Create, investigate and/or manage nonconformances, as well as associated ship holds and product disposition.
• Investigate, compile and report on information necessary for executive management to assess if field actions/corrections and removals associated with Teleflex products is warranted.
• Work closely with Manufacturing sites, R&D, Suppliers, Supplier Quality, Marketing, Design Assurance, and Regulatory to investigate and document quality issues.
• Assist with compilation and analysis of product quality metrics for presentation to Global and business unit leadership.
• Utilize basic statistical techniques to identify rates, changes in trends or estimated occurrences based on bench and field data.
• Utilize sound technical writing to provide clear and concise written internal reports and support external communications as needed to respond to Product Quality issues.
• Assist during regulatory inspections and/or audits as required.
• Utilize SAP, Agile and other systems as warranted for data input and quality record maintenance.
• Communicate and escalate Quality issues appropriately to QA Manager and address other items as assigned by Manager.
• Adhere to and ensure compliance with the Teleflex Code of Ethics, all company policies, rules, and procedures.
Education / Experience Requirements
• BS Degree in Engineering (or related technical field).
• 0-2 years related (medical device preferred) experience.
Specialized Skills / Other Requirements
• Computer literate (i.e., statistical software and analysis, excel, word processing for report generation, PowerPoint presentations, etc.).
• Positive attitude and ability to operate and communicate effectively with multiple teams & leadership.
• Ability to reason, support and prioritize projects, adapt to shifting priorities, effectively solve problems / conflicts, and proactively effect change.
INDIVIDUAL CONTRIBUTORS: Core competencies of all roles
• 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.
#LI-EB1
Working Conditions / Physical Demands
TRAVEL REQUIRED: Up to 15%
WORKING ENVIRONMENT:
☒ Office/Professional ☐ Plant/Manufacturing ☐ Remote/Field ☐ Laboratory
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.
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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