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Medical Device Quality Control Jobs in Utah (NOW HIRING)

Zimmer, Inc.

UT · On-site

$130K - $160K/yr

... medical device design and manufacturing site. Utilizes quality statistics to develop effective ... Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team ...

Zimmer, Inc.

Senior Quality Manager

Murray, UT · On-site

$130K - $160K/yr

... medical device design and manufacturing site. Utilizes quality statistics to develop effective ... Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team ...

Zimmer, Inc.

Senior Quality Manager

Salt Lake City, UT · On-site

$130K - $160K/yr

... medical device design and manufacturing site. Utilizes quality statistics to develop effective ... Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team ...

Amrize

Quality Control Technician

Salt Lake City, UT

$18.25 - $23.25/hr

We're seeking a Quality Control Technician who's ready to be part of a people-first company ... Medical, Dental, Disability and Life Insurance Coverage * Holistic Health & Well-Being Programs

QUIKRETE Companies

Quality Control Technician

Moab, UT · On-site

$18.75 - $24.25/hr

Medical, Dental, Vision, Company paid life and disability benefits, paid vacation, and 401K. About the Role Responsibilities: * Perform QC tests (air content, slump/workability, coarseness/sandiness ...

Amrize

Quality Control Technician

Salt Lake City, UT · On-site

$18.25 - $23.25/hr

We're seeking a Quality Control Technician who's ready to be part of a people-first company ... Medical, Dental, Disability and Life Insurance Coverage * Holistic Health & Well-Being Programs

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Medical Device Quality Control information

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

As of Jul 28, 2026, the average hourly pay for medical device quality control in Utah is $19.55, according to ZipRecruiter salary data. Most workers in this role earn between $15.77 and $21.88 per hour, depending on experience, location, and employer.

What are some common challenges faced in a Medical Device Quality Control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

What is the difference between Medical Device Quality Control vs Medical Device Quality Assurance?

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

What is quality control in medical devices?

Quality control in medical device manufacturing involves inspecting and testing products to ensure they meet safety, performance, and regulatory standards. Medical device quality control professionals use tools like calibration, documentation, and statistical analysis to identify defects and maintain product consistency throughout production. Compliance with standards such as ISO 13485 is essential in this role.

What is Medical Device Quality Control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

Is quality control still a job?

Yes, quality control remains a vital role in the medical device industry, ensuring products meet safety and regulatory standards. Quality control professionals typically perform inspections, testing, and documentation, often requiring knowledge of industry regulations and tools like calibration equipment. The role continues to be essential for maintaining product quality and compliance.

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

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.

Do you need a degree for QC?

For a Medical Device Quality Control position, a degree is often preferred but not always required; relevant experience, technical skills, and certifications such as ISO or Six Sigma can also be valuable. Employers may consider candidates with strong attention to detail and knowledge of quality standards even without a formal degree.

What medical device company pays the most?

In the medical device industry, senior quality control roles often have higher salaries, especially at large multinational companies like Medtronic, Abbott, and Johnson & Johnson. Compensation varies based on experience, location, and certifications such as ISO or Six Sigma, but top-paying companies tend to offer competitive salaries for experienced professionals in quality assurance and control positions.
What are popular job titles related to Medical Device Quality Control jobs in Utah? For Medical Device Quality Control jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Medical Device Quality Control jobs in Utah look for? The top searched job categories for Medical Device Quality Control jobs in Utah are:
What cities in Utah are hiring for Medical Device Quality Control jobs? Cities in Utah with the most Medical Device Quality Control job openings:
Medical Device Quality Control jobs near you
Infographic showing various Medical Device Quality Control job openings in Utah as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $40,665 per year, or $19.6 per hour.

Senior Quality Manager

Zimmer, Inc.

UT • On-site

$130K - $160K/yr

Other

This job post has expired today. Applications are no longer accepted.

Job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.


What You Can Expect


This is an onsite role at our site in Norfolk, Virginia
Site Quality leader and Management Representative responsible for directing the quality function a medical device design and manufacturing site. Utilizes quality statistics to develop effective strategies to maintain and improve the performance of products and the quality system. Develops relationships with key development and manufacturing peers to identify emerging needs. Resolves complex problems that have implications beyond own area. Requires professional expertise and interpersonal skills to manage multiple projects and interface with personnel from all company disciplines and business units. Takes accountability, achieves results and develops self and others.

How You'll Create Impact
  • Develop and implement site-wide quality strategy aligned with corporate objectives and regulatory requirements (QMSR, GMP, ISO, and other global standards) including objectives, and planning to support the strategy.
  • Establish and refine key quality metrics, ensuring data-driven decision-making to enhance product integrity and regulatory compliance.
  • Partner with R&D, supply chain, manufacturing, and distribution teams to enhance quality processes across the product lifecycle and drive cross-functional teamwork to improve operational efficiencies, ensuring seamless integration of quality in all aspects of pharmaceutical production.
  • Serve as the primary quality representative during regulatory inspections and audits, ensuring adherence to industry and corporate standards.
  • Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team, fostering a culture of collaboration and accountability.
  • Empower team to lead investigations into deviations, CAPA (Corrective and Preventive Actions), and change control processes to improve operational resilience and ensure timely product release and market supply by resolving quality-related issues effectively
What Makes You Stand Out
  • Must have a thorough knowledge of QMSR, GMP, ISO and other relevant regulatory requirements as applied to medical device development, manufacturing and distribution.
  • Demonstrated independent decision-making ability applying regulations and standards related to the manufacturing and distribution of medical device products.
  • Demonstrated management ability including organizational design and employee selection, development, motivation and performance.
  • Demonstrated ability to achieve productivity goals collaboratively without sacrificing quality in a manufacturing environment.
  • Demonstrated understanding of interactions and interdependency of elements within the quality system in a pharmaceutical manufacturing organization.
  • Must be able to work with all levels of employees, including hourly production employees through senior management.
  • Must possess excellent written and oral communication skills and the demonstrated ability to communicate with individuals of varying backgrounds.
Your Background
  • A Bachelor's Degree in a technical field is required
  • 7-10 years of work experience in medical device quality, preferably in manufacturing environments
  • 5 years' experience with direct management responsibility
  • CQE/CQM preferred


Expected Compensation: $130,000- $160,000 base salary. Role also comes with a comprehensive bonus.


EOE

Employment Type: OTHER

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