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Validation Associate Jobs in Minnesota (NOW HIRING)

Forj Medical

Validation Engineer, Senior

Saint Paul, MN · On-site

$100K - $115K/yr

... associates on validation concepts to strengthen integration of the validation program into the manufacturing organization. Job Duties and Responsibilities Validation Program Ownership * Develop ...

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 ...

Parman Energy

Warehouse Associate

Saint Cloud, MN

$18/hr

Warehouse Associate (Seasonal) Location: St. Cloud, MN Starting Salary: $18/hour+ based on ... Valid Driver's License * Frequent standing/walking and the ability to lift and move up to 100lbs

Bio-Techne

Senior Research Associate

Minneapolis, MN · On-site

$62K - $102K/yr

Pay Range: $62,300.00 - $102,350.00 Antibody Validation Group | Customer Applications | R&D WHY ... POSITION SUMMARY We are seeking a highly skilled and motivated Senior Research Associate to join ...

Bio-Techne

Senior Research Associate

Minneapolis, MN

$62K - $102K/yr

Pay Range: $62,300.00 - $102,350.00 Antibody Validation Group | Customer Applications | R&D WHY ... POSITION SUMMARY We are seeking a highly skilled and motivated Senior Research Associate to join ...

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All JobsValidation Associate JobsValidation Associate Jobs in Minnesota

Validation Associate information

See Minnesota salary details

$22

$50

$76

How much do validation associate jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for validation associate in Minnesota is $50.93, according to ZipRecruiter salary data. Most workers in this role earn between $38.61 and $61.92 per hour, depending on experience, location, and employer.

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

To thrive as a Validation Associate, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory compliance standards such as GMP or FDA guidelines. Familiarity with validation software, laboratory instrumentation, and documentation management systems is typically required, and certifications like Lean Six Sigma can be beneficial. Attention to detail, problem-solving abilities, and effective communication are essential soft skills in this role. These skills ensure that processes, equipment, and systems meet regulatory requirements and quality standards, which is critical for product safety and organizational compliance.

What is the difference between Validation Associate vs Quality Control Analyst?

AspectValidation AssociateQuality Control Analyst
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQ often preferredBachelor's degree in chemistry, biology, or related field; certifications like CQE or ASQ common
Work EnvironmentPharmaceutical, biotech, or medical device manufacturing facilities; focus on validation processesLaboratories, manufacturing plants; focus on testing and quality assessment
Employer & Industry UsageUsed in regulated industries requiring validation of processes and systemsCommon in quality testing, inspection, and product release processes

While both roles require a background in science and similar certifications, a Validation Associate primarily focuses on validating processes and systems to ensure compliance, whereas a Quality Control Analyst concentrates on testing products and materials to verify quality. Both roles are essential in regulated industries but serve different functions within the quality assurance framework.

What are Validation Associates?

Validation Associates are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet required standards and regulations. They plan and execute validation protocols to confirm that products are produced consistently and meet quality specifications. Their work involves documenting procedures, performing tests, analyzing data, and maintaining compliance with regulatory agencies such as the FDA. Validation Associates play a critical role in quality assurance and risk management within their organizations.

How does a Validation Associate typically collaborate with other departments during a project?

A Validation Associate frequently works cross-functionally with teams such as Quality Assurance, Manufacturing, and Research & Development. They coordinate to gather essential documents, understand process requirements, and ensure that all validation activities meet regulatory standards. Effective communication and organization are key, as Validation Associates often facilitate meetings, resolve discrepancies, and provide updates to stakeholders. This collaborative approach helps maintain compliance and supports the successful launch or improvement of products and processes.
What are popular job titles related to Validation Associate jobs in Minnesota? For Validation Associate jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Validation Associate jobs in Minnesota look for? The top searched job categories for Validation Associate jobs in Minnesota are:
Validation Associate jobs near you
Infographic showing various Validation Associate job openings in Minnesota as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $105,926 per year, or $50.9 per hour.

Validation Technician I

STERIS Laboratories, Inc.

Brooklyn Park, MN • On-site

$25.03 - $32.40/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 days ago

Job description

Position Summary

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

Validation Technicians in the Applied Sterilization Technologies (AST) Brooklyn Park, Minnesota location are responsible for Customer process validation execution. They work closely with the TechTeam and/or the Customer to assure the protocols are executed with care and are documented properly. Generates accurate records evidencing completion of these activities and maintains laboratory spaces and supplies.

Pay range: $25.03 - $32.40 per hour based on experience.

Shift: Monday - Friday 8:00am - 5:00pm (start time can be flexible)

What You'll Do as a Validation Technician I

Operational Excellence (100%)

  • Maintains proper data collection used in validations and qualifications per procedure or protocol requirements.
  • Executes Customer process validations for moist heat, reusable device, and liquid chemical sterilizations or engineering studies. Generates study documentation.
  • Operates processing and testing equipment as applicable for Customer studies and as directed by TechTeam.
  • Ensures processes and equipment are maintained in a validated state by supporting revalidation runs following changes.
  • Investigates unexpected test results and proposes solutions to process deviations and Customer complaints. Supports updates to procedures related to their responsibilities.
  • Contributes to safe and accurate execution by notifying Manager of any event, item or documentation that may have a concern in regard to regulatory or specification compliance, process quality, or employee safety.
  • Assists in the performance and adherence to ISO requirements.
  • Strives for continuous improvement by analyzing new or alternative ways to improve operations; incorporates recommendations into analysis.
  • Contributes in a team effort by performing in accordance to all STERIS policies, GMP, Lean principles and other directives; supports the directives and decisions of higher-level management and performs other duties as assigned.
  • Supports the STERIS AST business imperatives of Growth, Operational Excellence, Leadership Excellence and Customer Focus.
The Experience, Skills and Abilities Needed
  • Associate's or Bachelor's Degree preferred with a minimum of one (1) year of experience in sterilization, laboratory, or related industry. In lieu of degree, 4 years of related experience.
  • Pass Boiler Operator training program, preferred.
  • Ability to lift up to 25lb.
  • Ability to effectively write and verbally communicate in English.
  • Ability to work independently under general direction and supervision.
  • Effective interpersonal skills as demonstrated through priorexperience.
  • Requires ability to navigate through defined computer screens.
  • Above average experience organizing and analyzing, and utilizing Level 2 math skills (four basic arithmetic functions in all units of measurement, decimals ratios, rates, percentages) to perform compliant data handling and data analysis.
  • Ability to adapt to changing duties and responsibilities.
  • Normal hearing range sufficient to hear alarms, bells, horns, etc.
What STERIS Offers

We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future.

Here is just a brief overview of what we offer:

    • Market Competitive Pay
    • Extensive Paid Time Off and (8) added holidays
    • Excellent Healthcare, Dental and Vision Benefits
    • Long/Short Term disability coverage
    • 401(k) with company match
    • Maternity & Paternal Leave
    • Additional add-on benefits/discounts for programs such as Pet Insurance
    • Tuition Reimbursement and continued educations programs
    • Excellent opportunities for advancement and stable long-term career

Pay range for this opportunity is$25.03-$32.40. This position is eligible for bonus participation.

Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.

STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits

Open until position is filled.

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit www.steris.com.

If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.

STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

The full affirmative action program, absent the data metrics required by 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours.

Employment Type: FULL_TIME

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