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Validation Jobs in Minnesota (NOW HIRING)

The Validation Engineer will collaborate with cross-functional teams to support project execution from design qualification through commissioning, verification, and qualification activities.

Your Role We are seeking a Validation Engineer to support the validation of facilities, utilities, and equipment within a regulated pharmaceutical or biotechnology environment. The successful ...

Validation Engineer

Minneapolis, MN · On-site

$90 - $105/hr

Your Role We are seeking a Validation Engineer to support the validation of facilities, utilities, and equipment for a centrifuge implementation project within a regulated pharmaceutical or ...

Validation Engineer

Minneapolis, MN · On-site

$90K - $105K/yr

The Validation Engineer will collaborate with cross-functional teams to support project execution from design qualification through commissioning, verification, and qualification activities.

Validation Engineer

Jackson, MN · On-site

$54K - $100K/yr

Our work is tightly integrated with validation teams to ensure designs meet functional and durability standards. Downstream, we engage with manufacturing, quality, and marketing to ensure smooth ...

Validation Engineer

Jackson, MN · On-site

$54K - $100K/yr

Our work is tightly integrated with validation teams to ensure designs meet functional and durability standards. Downstream, we engage with manufacturing, quality, and marketing to ensure smooth ...

Validation Engineer

Jackson, MN · On-site

$54K - $100K/yr

Our work is tightly integrated with validation teams to ensure designs meet functional and durability standards. Downstream, we engage with manufacturing, quality, and marketing to ensure smooth ...

Your Role The Cleaning Validation Engineer is responsible for the development, modification, execution, and reporting of cleaning validation activities supporting biopharmaceutical manufacturing ...

Your Role The Cleaning Validation Engineer is responsible for the development, modification, execution, and reporting of cleaning validation activities supporting biopharmaceutical manufacturing ...

Your Role The Cleaning Validation Engineer is responsible for the development, modification, execution, and reporting of cleaning validation activities supporting biopharmaceutical manufacturing ...

You will lead validation planning and testing efforts for snowmobile platforms, ensuring systems and components meet defined performance, reliability, and durability requirements. In this role, you ...

Your Role The Cleaning Validation Engineer is responsible for the development, modification, execution, and reporting of cleaning validation activities supporting biopharmaceutical manufacturing ...

You will lead validation planning and testing efforts for snowmobile platforms, ensuring systems and components meet defined performance, reliability, and durability requirements. In this role, you ...

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Showing results 1-20

Validation information

See Minnesota salary details

$22

$50

$76

How much do validation jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for validation 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 is a validation job?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.

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

To thrive as a Validation Engineer, you need a solid background in engineering or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

What does a validation specialist do?

A validation specialist is responsible for ensuring that processes, equipment, and systems meet regulatory standards and quality requirements. They develop, execute, and document validation protocols, often working with industries like pharmaceuticals, biotech, or manufacturing, and may use tools such as validation software and perform risk assessments. Certification and attention to detail are important in this role.

What are the most commonly searched types of Validation jobs in Minnesota?

The most popular types of Validation jobs in Minnesota are:

Infographic showing various Validation job openings in Minnesota as of August 2026, with employment types broken down into 89% Full Time, 3% Part Time, and 8% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $105,926 per year, or $50.9 per hour.

Validation Engineer

PSC Biotech

Minneapolis, MN • On-site

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago


Job description


PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.
Our goal is to skyrocket our clients' success, and you can be a part of our team's achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success.
The Experience
With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.
We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.
At PSC Biotech®, it's about more than just a job-it's about your career and your future.
Your Role
We are seeking a Validation Engineer to support the validation of facilities, utilities, and equipment within a regulated pharmaceutical or biotechnology environment. The successful candidate will be responsible for developing, executing, and documenting validation activities throughout the system lifecycle, ensuring compliance with applicable quality standards and regulatory requirements. The Validation Engineer will collaborate with cross-functional teams to support project execution from design qualification through commissioning, verification, and qualification activities.
  • Support validation activities for facilities, utilities, and equipment systems.
  • Develop, author, review, and execute validation protocols and reports within the KNEAT platform.
  • Support lifecycle validation deliverables from risk assessment through commissioning, qualification (IQ/OQ/PQ), and final verification.
  • Collaborate with Engineering, Quality, Operations, and project teams to ensure validation deliverables are completed in accordance with project timelines.
  • Execute field verification and qualification testing activities and document results.
  • Identify, evaluate, and mitigate validation-related risks using a risk-based validation approach.
  • Ensure validation documentation is complete, accurate, and compliant with cGMP and quality requirements.
  • Support deviation investigations, change controls, and corrective actions associated with validation activities.
  • Maintain compliance with client site training requirements, SOPs, and quality standards.
  • Communicate project status, validation progress, and technical findings to project stakeholders.
  • Support audits, inspections, and validation documentation reviews as required.

Requirements
  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
  • 3+ years of validation, CQV, or qualification experience within pharmaceutical, biotechnology, or regulated manufacturing environments.
  • Hands-on experience using KNEAT for validation protocol development, execution, and approval workflows required.
  • Experience validating facilities, utilities, process equipment, and manufacturing systems.
  • Strong understanding of validation lifecycle methodologies, including risk assessments, DQ, commissioning, verification, IQ, OQ, and PQ.
  • Experience supporting process equipment, or similar manufacturing systems preferred.
  • Working knowledge of cGMP regulations and industry guidance, including FDA and ISPE principles.
  • Excellent technical writing, documentation, and protocol execution skills.
  • Strong analytical, troubleshooting, and problem-solving abilities.
  • Effective communication skills with the ability to work independently and within cross-functional team.
  • Must be authorized to work in the U.S.
  • No C2C at this time.

Benefits
Offering a full suite of benefits, PSC Biotech™ is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.
  • Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
  • Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more.
  • 401(k) and 401(k) matching
  • PTO, Sick Time, and Paid Holidays
  • Education Assistance
  • Pet Insurance
  • Fitness Benefits (Membership discounts and other perks/services at qualifying gyms like Anytime Fitness, 24-Hour Fitness, and more)
  • Financial Perks and Discounts

The salary bracket for this role is set between $90,000 - $105,000 annually. The salary offered may be adjusted based on various factors such as the applicant's qualifications, skills, and professional experience.
Equal Opportunity Employment Statement
PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs,including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant's, employee's, or intern's actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.
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