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Quality Manager Medical Device Jobs in Raleigh, NC

Manage third-party environmental testing and approve results * Support sterilization coordination ... Preferred: * 5+ years in medical device manufacturing * Experience with quality operations, design ...

You manage customer quality activities, including audits, complaints, quality agreements, and ... Medical, Dental, and Vision Insurance Basic Life Insurance & Accidental Death & Dismemberment (AD&D ...

QA Manager

Garner, NC ยท On-site

You lead the site's Quality Management System, ensuring compliance with GMP, ISO, BRCGS, customer ... Medical, Dental, and Vision Insurance * Basic Life Insurance & Accidental Death & Dismemberment (AD ...

QA Manager

Garner, NC ยท On-site

You manage customer quality activities, including audits, complaints, quality agreements, and ... Medical, Dental, and Vision Insurance Basic Life Insurance & Accidental Death & Dismemberment (AD&D ...

Quality Engineer I

Durham, NC ยท On-site

$69K - $89K/yr

... industry such as health care, medical device, pharmaceutical, etc). Desired Experience ... Ability to work independently with strong time management and prioritization skills to handle ...

... high-quality products through rigorous testing, documentation, and risk management ... Ensure compliance with relevant medical device industry regulations and standards, including FDA ...

... high-quality products through rigorous testing, documentation, and risk management ... Ensure compliance with relevant medical device industry regulations and standards, including FDA ...

Quality Assurance Associate

Raleigh, NC ยท On-site

$60 - $80/hr

Manage and initiate regional testing for the annual update of the Business Continuity Plan * Assist ... and medical device firms. For more information, visit www.ctifacts.com Why CTI? * Advance Your ...

Showing results 41-60

Quality Manager Medical Device information

See Raleigh, NC salary details

$23.3K

$83.7K

$153.6K

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

As of Sep 8, 2026, the average yearly pay for quality manager medical device in Raleigh, NC is $83,749.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,800.00 and $132,200.00 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 Operations Specialist

GILERO

Pittsboro, NC โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago


Job description

Do you have a passion for helping bring innovative medical devices and drug delivery products to market that improve patient lives? Gilero, a Sanner Group company, is seeking an experienced Quality Operations Specialist to support our Pittsboro, NC facility. You will be responsible for Quality Operations to support transition between development and commercial manufacturing activities.

Duties:

  • Liaise between product development and manufacturing project teams to ensure compliant design transfer
  • Coordinate, assemble, and route documentation per quality system lifecycle requirements
  • Perform incoming inspection/testing and release of accepted materials
  • Perform pilot builds in cooperation with operations and design transfer teams
  • Conduct labeling verification in accordance with product requirements
  • Perform in-process testing and QA inspections per product requirements
  • Coordinate environmental monitoring, including particle counts and temperature/humidity/pressure measurements
  • Coordinate cleaning of controlled environment areas per internal procedures
  • Manage third-party environmental testing and approve results
  • Support sterilization coordination
  • Review batch records for accuracy and completeness. Collaborate with manufacturing and development teams to resolve any batch documentation-related errors or gaps
  • Support quality event initiation and investigation for nonconformances, CAPA, change control and complaints.
  • Support continuous improvement projects and audits

Skills/Qualifications:

  • Bachelor’s degree or equivalent combination of education and experience.
  • 0 - 5 years in regulated manufacturing environment
  • Experience with FDA 820 CFRs/ISO 13485/cGMP quality management system requirements and medical devices/combination product development
  • Basic experience with coordination of GMP compliant Documents, Records, and Training
  • Strong written and verbal communication skills
  • Preferred:
  • 5+ years in medical device manufacturing
  • Experience with quality operations, design transfer and GxP concepts
  • Experience with GMP manufacturing operations and process development
  • ASQ or related certification

Personal Attributes:

  • Meets Gilero Core Values: Collaboration, Innovation, Excellence, Integrity
  • Productive in a fast-paced, entrepreneurial environment.
  • Commits to excellence and quality service to external and internal customers.
  • Adheres to established policies and procedures, while contributing to continuous improvements.

Eligibility To Work

  • Applicants must be permanently authorized to work in the United States without the need for employer sponsorship now or in the future.
  • Gilero does not offer sponsorship for employment authorizations (work visas).
  • We are an E-Verify employer and confirm work authorization for all new hires.

Why work at Gilero?
Founded in 2002, Gilero, a Sanner Group company, is an international contract engineering firm that specializes in the design, development, and manufacturing of novel medical devices and drug delivery products. At Gilero we are proud of the culture we have built that directly reflects our values of excellence, integrity, innovation, and collaboration. Motivated by our purpose to benefit people and improve patient outcomes, our teams continue to grow at a rapid pace. US locations include Carlsbad, CA; Chicago, IL; as well as NC locations in Durham, Greensboro, and Pittsboro.

You will enjoy an annual bonus plan, Medical (3 BCBS plans to choose from), dental and vision, company provided life insurance, short-term and long-term disability, 401(k) with a match the first month after you start with a zero-vesting period, and access to LinkedIn learning for personal and professional development.

What We Offer 

  • Competitive base salary plus incentive compensation
  • Annual performance bonus
  • Medical, dental, and vision insurance (multiple BCBS medical plan options)
  • Company paid life insurance, short- and long-term disability coverage
  • 401(k) with company match beginning the first month after you start and immediate vesting in company match 
  • Paid parental leave
  • Paid Time Off and company holidays
  • LinkedIn Learning for professional development
  • Career growth opportunities within Gilero and the global Sanner Group

Gilero logo

About Gilero

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

51 - 200 Employees

Headquarters location

Durham, NC, US

Year founded

2002

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