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Senior Quality Control Associate Jobs in Minnesota

Senior Quality Engineer

New Hope, MN · On-site

$91K - $124K/yr

This Sr Quality Engineer is primarily responsible for providing technical support to ensure ... They should also have experience providing effective technical support and Supervision to the QC/QA ...

At Lakeshirts, every garment has a destination, and the Quality Control team helps make sure it gets there looking ah-mazing. This role is a great fit for someone who notices the little things, works ...

Quality Control

Detroit Lakes, MN · On-site

$17 - $22/hr

At Lakeshirts, every garment has a destination, and the Quality Control team helps make sure it gets there looking ah-mazing. This role is a great fit for someone who notices the little things, works ...

At Lakeshirts, every garment has a destination, and the Quality Control team helps make sure it gets there looking ah-mazing. This role is a great fit for someone who notices the little things, works ...

Quality Control

Mankato, MN · On-site

$25.30 - $28.80/hr

... Quality Assurance, System Operator. Administration roles such as Human Resource Clerk and Office ... part-time associates in Walmart and Sam's Club facilities. Programs range from high school ...

Senior Quality Engineer

Saint Paul, MN · On-site

$92K - $98K/yr

What You'll Do The Senior Quality Engineer is responsible for leading advanced quality initiatives ... Lead the development, implementation, and optimization of advanced quality control processes to ...

Sr. Quality Engineer

Chaska, MN · On-site

$120K - $130K/yr

This Senior role is responsible for providing support for design verification and validation activities while ensuring compliance to IMRIS design control procedures, Quality Management Systems ...

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Senior Quality Control Associate information

See Minnesota salary details

$11

$24

$37

How much do senior quality control associate jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for senior quality control associate in Minnesota is $24.94, according to ZipRecruiter salary data. Most workers in this role earn between $18.12 and $30.38 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a senior quality control associate?

To thrive as a Senior Quality Control Associate, you need a strong background in analytical testing, quality assurance principles, and relevant scientific education, often with a bachelor’s degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and regulatory compliance requirements is typically expected, along with proficiency in using laboratory instruments. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for excelling in this role. These competencies ensure the reliability of product quality, support regulatory compliance, and contribute to efficient cross-functional collaboration within the organization.

What are some typical challenges senior quality control associates face when overseeing multiple projects simultaneously?

Senior Quality Control Associates often manage several projects at once, which can present challenges such as balancing competing deadlines, ensuring consistent application of quality standards, and effectively communicating with cross-functional teams. Staying organized and prioritizing tasks is essential to prevent bottlenecks and maintain high-quality deliverables. Additionally, adapting quickly to changes in project scope or regulatory requirements is a key part of the role, as is mentoring junior team members to uphold best practices.

What is the difference between Senior Quality Control Associate vs Quality Control Associate?

AspectSenior Quality Control AssociateQuality Control Associate
Required CredentialsBachelor's degree, relevant certifications (e.g., CQE)Bachelor's degree often preferred, certifications optional
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or production settings
Employer & Industry UsagePharmaceuticals, biotech, manufacturing companiesPharmaceuticals, biotech, manufacturing companies
Job ResponsibilitiesOversees testing, reviews quality data, mentors junior staffPerforms testing, documents results, supports quality checks

The main difference between a Senior Quality Control Associate and a Quality Control Associate lies in experience, responsibilities, and leadership. Senior roles typically involve overseeing testing processes, mentoring staff, and ensuring compliance, while associate roles focus on executing tests and documenting results. Both positions are vital in maintaining product quality in industries like pharmaceuticals and manufacturing.

What does a senior quality control associate do?

A Senior Quality Control Associate is responsible for overseeing and performing quality control tests on products or materials to ensure they meet company and regulatory standards. They analyze test data, identify trends or deviations, and help implement corrective actions when issues are found. Additionally, they may mentor junior team members, assist in developing testing protocols, and collaborate with other departments to resolve quality concerns. Their work is essential in maintaining product consistency, safety, and compliance within the organization.
What cities in Minnesota are hiring for Senior Quality Control Associate jobs? Cities in Minnesota with the most Senior Quality Control Associate job openings:

Sr. Quality Control Supervisor

Cirtec Medical Corporation

Brooklyn Park, MN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 26 days ago


Cirtec Medical rating

6.6

Company rating: 6.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz


Job description

Description
About us:
For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems.
Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team!
Position Summary:
The Senior Supervisor, Quality Control leads daily quality control operations to ensure products meet internal standards, regulatory requirements, and customer expectations. This role partners closely with Engineering and Production to support manufacturing schedules, drive continuous improvement, and maintain compliance with applicable quality systems (e.g., GMP, GDP). The position also plays a key role in team leadership, problem-solving, and process optimization.
Key Responsibilities:
  • Lead and prioritize quality control activities to support production and engineering needs.
  • Supervise inspection activities, including incoming, in-process, and final product inspections.
  • Coach, develop, and manage quality inspectors and technicians; support onboarding and training.
  • Partner with Quality Engineering on investigations, root cause analysis, and corrective actions.
  • Oversee disposition of nonconforming materials and support material review processes.
  • Monitor inspection data, identify trends, and drive improvements using SPC and data analysis.
  • Ensure compliance of Device History Records (DHRs) with GMP and GDP requirements.
  • Develop, maintain, and improve inspection plans, procedures, and quality control documentation.
  • Support product transfers from development to production, ensuring quality readiness.
  • Coordinate measurement system analysis (MSA) activities and inspection methods.
  • Verify environmental monitoring results and support cleanroom compliance, as applicable.
  • Generate Certificates of Conformity and maintain accurate quality records in PLM systems.
  • Recommend tools, equipment, and process improvements to enhance quality and efficiency.

Must Have:
  • Bachelor's degree in Quality, Engineering, or a related STEM field (or equivalent experience).
  • 5-7 years of experience in Quality Control/Quality Assurance, preferably in the medical device industry.
  • Prior supervisory or team leadership experience required.
  • Strong knowledge of GMP, GDP, and quality systems in a regulated environment.
  • Experience with SPC, root cause analysis, and continuous improvement methodologies.
  • Proficiency in Microsoft Office (Excel, Word, PowerPoint) and quality data analysis tools.
  • Strong communication, organizational, and problem-solving skills.
  • Ability to effectively lead teams, manage performance, and resolve conflicts.

Good to have:
  • ASQ certifications (e.g., CQI, CQT, Six Sigma Green Belt) preferred.

Salary Range: 80,000 to 127,000 based on skills and experience.
Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.
We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec's goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Our benefits include Training and career development, Healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs, Paid Time Off and 401(k) retirement savings with a company match.

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