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Quality Associate Jobs in Savage, MN (NOW HIRING)

Danaher

Manager Quality Assurance, Validation

Chaska, MN · On-site

$130K - $160K/yr

This position will manage professional associates and operation support assigned to the Quality Assurance line support and validation team management, equipment program management, Design Change ...

Danaher

Manager Quality Assurance, Validation

Chaska, MN · On-site

$130K - $160K/yr

This position will manage professional associates and operation support assigned to the Quality Assurance line support and validation team management, equipment program management, Design Change ...

Phillips and Temro

QA Tech - Associate

Delano, MN · On-site

$20 - $25/hr

Maintain incoming quality inspection files including, but not limited to: current print revision levels, material certifications, and inspection logs, Supplier Part Approvals. * Update and maintain ...

Australia-Employment

Quality Supervisor

Chaska, MN · On-site

$90 - $110/hr

Champion a culture of quality by coaching associates, reinforcing standards, and helping build quality ownership across all levels of the organization * Own and continuously improve the quality ...

New

Oatey

Quality Validation Engineer

Shakopee, MN · On-site

$85K - $103K/yr

Operate, maintain, and train associates on key analytical equipment and software used for technical quality analysis. Knowledge and Experience: Required * Three (3) to five (5) years of Quality ...

Oatey

Quality Validation Engineer

Shakopee, MN

$85K - $103K/yr

Operate, maintain, and train associates on key analytical equipment and software used for technical quality analysis. Knowledge and Experience: Required Three (3) to five (5) years of Quality ...

Oatey

Quality Validation Engineer

Shakopee, MN

$85K - $103K/yr

Operate, maintain, and train associates on key analytical equipment and software used for technical quality analysis. Knowledge and Experience: Required * Three (3) to five (5) years of Quality ...

Oatey Es

Quality Validation Engineer

Shakopee, MN · On-site

$85K - $103K/yr

Operate, maintain, and train associates on key analytical equipment and software used for technical quality analysis. Knowledge and Experience: Required Three (3) to five (5) years of Quality ...

Oatey

Quality Validation Engineer

Shakopee, MN

$85K - $103K/yr

Operate, maintain, and train associates on key analytical equipment and software used for technical quality analysis. Knowledge and Experience: Required * Three (3) to five (5) years of Quality ...

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All JobsQuality Associate JobsQuality Associate Jobs in Savage, MN

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How much do quality associate jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for quality associate in Savage, MN is $28.73, according to ZipRecruiter salary data. Most workers in this role earn between $19.47 and $33.61 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

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

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

More about Quality Associate jobs

What are the most commonly searched types of Quality jobs in Savage, MN?

The most popular types of Quality jobs in Savage, MN are:

What job categories do people searching Quality Associate jobs in Savage, MN look for?

The top searched job categories for Quality Associate jobs in Savage, MN are:

What cities near Savage, MN are hiring for Quality Associate jobs?

Cities near Savage, MN with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Savage, MN as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 3% Contract, and 2% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $59,755 per year, or $28.7 per hour.

Research Associate - ProteinSimple QC

Bio-Techne

Minneapolis, MN • On-site

$40K - $66K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago

Bio-Techne rating

8.4

Company rating: 8.4 out of 10

Based on 15 frontline employees who took The Breakroom Quiz

Job description

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.
Pay Range:
$40,300.00 - $66,250.00
Position Summary:
Perform routine quality control testing to determine lot status and product release for the ProteinSimple capillary electrophoresis basis systems, including iCE and SimpleWestern. This position is responsible for planning, executing, and managing activities in the ProteinSimple liquid and lyophilized reagent QC process to ensure that all applicable objectives are met, and the product functions as expected. To be successful in this role candidate needs to be skilled in analytical techniques for analysis of biological assays. This position interfaces with Manufacturing, Process Engineering, Product Support, Assay Development and Quality Assurance.
Key Responsibilities:
  • Run QC assays for reagents and consumables, analyze results, and review trending data
  • Precise and meticulous observation and recording of all details of QC assay, which are not limited to but including: lot numbers, expiration dates, and physical observations of materials
  • Revise SOPs of low complexity
  • Initiate deviation and out-of-specification investigations
  • Keep a clean and organized workspace
  • Maintain inventory of reagents and consumables needed to perform QC assays
  • Participate in continuous process improvements efforts
  • Understand and follow appropriate lab protocols
    • Chemical handling and hazards
    • Labeling
    • Safety procedures
    • Department specific SOP's
    • Proper use and maintaining equipment
  • Follow guidelines and comply with all company safety, quality, and training procedures and regulations
  • Perform additional duties as assigned

Education and Experience:
  • Bachelor's degree in Biology, Chemistry, Engineering or similar science degree with 0-2 years of laboratory experience.
  • Associates degree or non- scientific bachelor's with 2+ years' relevant experience working in a quality position for a GMP or life science related industry.

Knowledge, Skills, and Abilities:
  • Ability to pipette and perform techniques like electrophoresis, isoelectric focusing, and western blotting
  • Basic understanding of electrophoresis techniques and data analysis.
  • Work independently with minimal supervision on routine tasks and follow priorities set by supervisor
  • Experience with MS Word, MS PowerPoint, MS Outlook, JMP, GraphPad Prism
  • Flexibility to work on multiple tasks with increased effectiveness
  • Strong organizational skills with an attention to detail and quality
  • Ability to support and help others in the team
  • Manages time well and will put in extended time as needed
  • Understanding of basic statistical principles

Why Join Bio-Techne:
  • We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
  • We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
  • We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
  • We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.
  • We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
  • We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

Bio-Techne is an E-Verify Employer in the United States.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.
This position requires work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States (e.g., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant work status). If you require a reasonable accommodation to complete an application, participate in an interview, or take part in any other stage of the recruitment process, please contact hr@bio-techne.com for assistance.

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