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Quality Manager Jobs in Rochester, MN (NOW HIRING)

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 ...

Strong understanding of Good Laboratory Practices (GLP) and quality management systems such as ISO 9001 and FSSC 22000. * Proficiency with Microsoft Office Suite applications, internet, or cloud ...

Must be able to provide management reports on trends and quality improvements. Ability to self ... manage and estimate to complete any given task around production schedules.

Quality Tech

Zumbrota, MN · On-site

$20 - $25/hr

Must be able to provide management reports on trends and quality improvements. Ability to self ... manage and estimate to complete any given task around production schedules. Salary Description $20 ...

Quality Tech

Zumbrota, MN · On-site

$20 - $25/hr

Must be able to provide management reports on trends and quality improvements. Ability to self ... manage and estimate to complete any given task around production schedules.

Quality Engineer

Rochester, MN · On-site

$100K - $130K/yr

The role focuses on risk management, deviation control, and lifecycle quality assurance, rather than execution of validation or process design. Key responsibilities include: * Lead and own deviation ...

Quality Engineer

Rochester, MN · On-site

$62K - $86K/yr

The Quality Engineer is responsible to develop, implement and maintain the Quality Assurance ... Ability to multi-task with excellent time management, problem prevention and problem-solving skills.

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Quality Manager information

See Rochester, MN salary details

$39.1K

$92.5K

$140.8K

How much do quality manager jobs pay per year?

As of Jul 21, 2026, the average yearly pay for quality manager in Rochester, MN is $92,549.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,700.00 and $111,800.00 per year, depending on experience, location, and employer.

What Does a Quality Manager Do?

As a quality manager, your job is to oversee Quality Assurance (QA) and Quality Control (QC) for each product or service assigned to you. Your duties include guaranteeing products and services meet the standards of your organization, keeping management aware of any problems with production, and ensuring that the manufacturing process goes as smoothly as possible. This job has different aspects depending on where a product or service is in the development cycle. Products that are still being designed need QA to make creation as smooth as possible, while released products require QC to ensure the expected level of quality is maintained.

How much do quality managers get paid?

Quality managers typically earn a median annual salary of around $70,000 to $110,000, depending on experience, industry, and location. They often hold certifications like Six Sigma or ISO auditor training and oversee quality assurance processes within organizations.

What are the key skills and qualifications needed to thrive as a Quality Manager, and why are they important?

To thrive as a Quality Manager, you need expertise in quality control processes, data analysis, and regulatory compliance, typically supported by a relevant degree and experience in quality management systems. Familiarity with ISO standards, Six Sigma, and software tools like Minitab or SAP is highly valued, along with certifications such as CQE or Six Sigma Green/Black Belt. Strong leadership, problem-solving abilities, and excellent communication are crucial soft skills for driving continuous improvement and facilitating cross-departmental collaboration. These skills ensure product and process excellence, regulatory adherence, and organizational efficiency.

What is the difference between Quality Manager vs Quality Supervisor?

AspectQuality Manager

Required CredentialsTypically requires a bachelor's degree in quality assurance, engineering, or related field; certifications like ASQ CQE or Six Sigma are common.
Work EnvironmentOversees multiple teams or departments, strategic planning, and process improvement initiatives.
Employer & Industry UsageUsed across manufacturing, healthcare, and service industries to lead quality programs.
Common Search & ComparisonOften compared with Quality Supervisor due to overlapping responsibilities and career progression.

The main difference between a Quality Manager and a Quality Supervisor lies in their scope and responsibilities. A Quality Manager focuses on strategic quality initiatives, process improvements, and managing teams at a higher level, often requiring advanced certifications. In contrast, a Quality Supervisor typically oversees daily operations, supervises staff directly, and implements quality procedures. Both roles are essential in maintaining quality standards, but the manager role involves broader planning and leadership functions.

What is the salary of a QA manager?

The salary of a Quality Assurance (QA) Manager typically ranges from $70,000 to $120,000 annually, depending on experience, industry, and location. Senior QA managers with specialized skills or certifications can earn higher salaries, and the role often involves overseeing testing teams and quality processes.

What is the role of a quality manager?

A quality manager oversees an organization’s quality assurance and control processes to ensure products or services meet specified standards and customer expectations. They develop quality policies, conduct audits, analyze data, and implement improvements, often using tools like Six Sigma or ISO standards. Strong leadership, attention to detail, and certification such as CQE or CQE are common requirements for this role.

What are some common challenges Quality Managers face when implementing new quality standards across teams?

Quality Managers often encounter resistance to change when introducing new quality standards, as team members may be accustomed to established processes. Ensuring consistent understanding and adoption across departments requires clear communication, comprehensive training, and ongoing support. Additionally, balancing the need for compliance with production deadlines can be challenging, so Quality Managers must collaborate closely with operations, engineering, and leadership teams to align goals and foster a culture of continuous improvement.

Is it hard to be a quality manager?

Being a quality manager involves overseeing quality assurance processes, implementing standards like ISO, and managing teams, which can require strong attention to detail, problem-solving skills, and certifications such as Six Sigma. The role can be demanding due to the responsibility for product or service quality and compliance, but it also offers opportunities for professional growth and leadership.
What are the most commonly searched types of Quality jobs in Rochester, MN? The most popular types of Quality jobs in Rochester, MN are:
What job categories do people searching Quality Manager jobs in Rochester, MN look for? The top searched job categories for Quality Manager jobs in Rochester, MN are:
What cities near Rochester, MN are hiring for Quality Manager jobs? Cities near Rochester, MN with the most Quality Manager job openings:
Infographic showing various Quality Manager job openings in Rochester, MN as of July 2026, with employment types broken down into 84% Full Time, 14% Part Time, 1% Temporary, and 1% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $92,549 per year, or $44.5 per hour.

$130K - $160K/yr

Other

Posted 12 days ago


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