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Senior Validation Engineer Jobs in Minnesota (NOW HIRING)

AGCO

Sr Field Validation Engineer

Jackson, MN · On-site

$95K - $115K/yr

The Sr Field Validation Engineer is responsible for conducting field tests on prototype agricultural and off-highway equipment and coordinating field testing activities for Application equipment ...

AGCO

Sr Field Validation Engineer

Jackson, MN

$95K - $115K/yr

The Sr Field Validation Engineer is responsible for conducting field tests on prototype agricultural and off-highway equipment and coordinating field testing activities for Application equipment ...

AGCO

Sr Field Validation Engineer

Jackson, MN · On-site

$95K - $115K/yr

The Sr Field Validation Engineer is responsible for conducting field tests on prototype agricultural and off-highway equipment and coordinating field testing activities for Application equipment ...

Polaris, Inc.

Sr. Hardware Validation Engineer

Wyoming, MN · On-site

$104K - $128K/yr

Collaborate with cross-functional engineering teams to resolve validation issues and support design updates. Desired Competencies: * Achievement Orientation Definition: Focusing efforts on achieving ...

Boston Scientific

Senior Quality Engineer

Arden Hills, MN · On-site

$92K - $125K/yr

... Senior Quality Engineer to develop, implement and maintain quality engineering systems ... You will play a critical role in process validation, risk management, process controls and ...

Boston Scientific

Senior Quality Engineer

Arden Hills, MN · On-site

$92K - $125K/yr

... Senior Quality Engineer to develop, implement and maintain quality engineering systems ... You will play a critical role in process validation, risk management, process controls and ...

Via Logic LLC

Senior DevSecOps Engineer

Eagan, MN · On-site

$108 - $195/hr

Senior DevSecOps Platform Engineer Leidos is seeking Senior DevSecOps Platform Engineers to join ... validated, and deployed rapidly while meeting the operational, security, and compliance ...

Leidos

Senior DevSecOps Engineer

Eagan, MN · On-site

$106K - $146K/yr

Senior DevSecOps Platform Engineer Leidos is seeking Senior DevSecOps Platform Engineers to join ... validated, and deployed rapidly while meeting the operational, security, and compliance ...

Leidos

Senior DevSecOps Engineer

Eagan, MN · Remote

$106K - $146K/yr

Senior DevSecOps Platform Engineer Leidos is seeking Senior DevSecOps Platform Engineers to join ... validated, and deployed rapidly while meeting the operational, security, and compliance ...

Health Staffing Group

Senior Process Engineer

Minneapolis, MN · On-site

$108K - $140K/yr

Senior Process Engineer About the Role The Senior Process Engineer will lead the development, validation, optimization, and continuous improvement of manufacturing processes within a regulated ...

Curtisswright

Senior Test Engineer

Chanhassen, MN · On-site

$100K - $125K/yr

As a Sr Test Engineer, you will lead the design, development, and execution of test strategies to validate products, systems, and manufacturing processes, serving as a technical authority and process ...

Curtiss-Wright

Senior Test Engineer

Chanhassen, MN · On-site

$100K - $125K/yr

As a Sr Test Engineer, you will lead the design, development, and execution of test strategies to validate products, systems, and manufacturing processes, serving as a technical authority and process ...

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Senior Validation Engineer information

See Minnesota salary details

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How much do senior validation engineer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for senior validation engineer in Minnesota is $63.44, according to ZipRecruiter salary data. Most workers in this role earn between $50.62 and $72.02 per hour, depending on experience, location, and employer.

What does a senior validation engineer do?

A Senior Validation Engineer is responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They develop and execute validation protocols, analyze test data, and document results to confirm compliance with industry and company standards. Senior Validation Engineers often lead validation projects, collaborate with cross-functional teams, and mentor junior staff. Their work is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where product safety and efficacy are essential.

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

To thrive as a Senior Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically supported by a relevant degree and experience in validation within regulated industries. Familiarity with validation protocols (IQ, OQ, PQ), statistical analysis tools, and systems like FDA 21 CFR Part 11 is crucial. Strong problem-solving, attention to detail, and effective communication skills help ensure successful project outcomes and cross-functional collaboration. These skills and qualifications are essential to maintain product quality, meet regulatory standards, and drive continuous improvement.

What are some typical challenges faced by senior validation engineers when leading validation projects?

Senior Validation Engineers often encounter challenges such as managing tight project timelines, ensuring compliance with evolving regulatory standards, and coordinating cross-functional teams. Balancing the needs of production, quality assurance, and regulatory affairs requires strong communication and project management skills. Additionally, troubleshooting unexpected validation failures and documenting results thoroughly are key aspects that demand both technical expertise and attention to detail.

What is the difference between Senior Validation Engineer vs Validation Specialist?

AspectSenior Validation EngineerValidation Specialist
CredentialsBachelor's or Master's in Engineering, Life Sciences, or related fields; often with certifications like GxP or CSVSimilar educational background; certifications like GxP or CSV are common
Work EnvironmentDesigns and oversees validation protocols in manufacturing, biotech, or pharmaceutical settingsExecutes validation tasks, tests, and documentation in similar environments
Employer & IndustryPharmaceutical, biotech, medical device companiesSame industries, often working under validation teams
Search & ComparisonOften compared for experience level and responsibilitiesCommonly searched together for validation roles

The main difference is that a Senior Validation Engineer typically leads validation projects, designs protocols, and oversees validation activities, while a Validation Specialist focuses on executing validation tests and documentation. Both roles require similar credentials and work in comparable environments, but the Senior Validation Engineer has more responsibility for planning and oversight.

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

The most popular types of Validation Engineer jobs in Minnesota are:

What are popular job titles related to Senior Validation Engineer jobs in Minnesota?

For Senior Validation Engineer jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Senior Validation Engineer jobs in Minnesota look for?

The top searched job categories for Senior Validation Engineer jobs in Minnesota are:

What cities in Minnesota are hiring for Senior Validation Engineer jobs?

Cities in Minnesota with the most Senior Validation Engineer job openings:

What are popular job titles related to Senior Validation Engineer jobs in MN?

For Senior Validation Engineer jobs in MN, the most frequently searched job titles are:

Senior Validation Engineer jobs near you
Infographic showing various Senior Validation Engineer job openings in Minnesota as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, 4% Contract, and 1% Nights. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $131,953 per year, or $63.4 per hour.

Senior Validation Engineer

PROMED MOLDED PRODUCTS INC

Plymouth, MN • On-site

$94K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 2 days ago

New

Job description

As a ProMed employee, you will contribute to the manufacture of products that have a significant impact on people’s lives. Through honesty, integrity, and collaboration, we strive to be the very best as we hire the very best.


ProMed was founded in 1989 addressing an industry need for cleanroom manufacturing of silicone components, specifically those having a medical application. We treat every component and finished device as though it will be used by a beloved family member or friend. We are dedicated to our customers and to our employees while helping to improve the health and well-being of people around the world.


Working as one to help many.


WHY THIS ROLE MATTERS

The mission of the Senior Engineer, Validation is to ensure that our facility, equipment, utilities, and manufacturing processes consistently perform as intended and remain in a state of control that satisfies cGMP and regulatory expectations. This role owns the technical rigor behind qualification and validation activities that give our clients and regulators confidence in every batch we produce.

The position requires deep technical expertise in process validation, strong document authorship and review skills, and the ability to lead validation activities across multiple concurrent client programs in a fast-paced CDMO environment.


The Senior Validation Engineer supports ProMed’s mission and values by applying and reinforcing the company’s brand, philosophy, systems, policies, and procedures are consistently applied and upheld in all aspects of their work.


WHAT YOU’LL ACHIEVE

While the ways that you fulfill these responsibilities will likely evolve, your core responsibilities are:

Validation Strategy & Master Planning

On average, this will represent about 30% of your time. In this aspect of your position, we will expect you to:

  • Author and maintain site and project-level Validation Master Plans (VMPs) defining scope, strategy, and lifecycle approach for equipment, utilities, and process validation.
  • Develop risk-based validation strategies that align with regulatory expectations (FDA, EMA, ICH Q7/Q8/Q9/Q10) and client requirements.
  • Establish and maintain validation policies, SOPs, and templates to support consistent execution across programs.
  • Partner with Quality Assurance to ensure validation approaches are appropriately risk-assessed and documented.

Process & Cleaning Validation (PQ/PPQ)

On average, this will represent about 45% of your time. In this aspect of your position, we will expect you to:

  • Author and execute Performance Qualification (PQ) and Process Performance Qualification (PPQ) protocols for manufacturing processes transferring from development to commercial-scale production.
  • Develop and execute cleaning validation protocols, including selection of worst-case products, swab/rinse sampling plans, and acceptance criteria based on toxicological limits (e.g., PDE/ADE).
  • Collaborate with Process Development and Manufacturing to define critical process parameters (CPPs) and critical quality attributes (CQAs) supporting validation acceptance criteria.
  • Analyze validation data and author final summary reports with statistically sound conclusions supporting process and cleaning validation status.
  • Support continued process verification (CPV) programs to maintain the validated state throughout the product lifecycle.

Cross-Functional Leadership & Client Support

On average, this will represent about 25% of your time. In this aspect of your position, we will expect you to:

  • Serve as validation subject matter expert (SME) for client-facing technical discussions, audits, and regulatory inspections.
  • Lead or support investigations into validation-related deviations, ensuring timely and technically sound root cause analysis and CAPA development.
  • Mentor junior validation engineers and provide technical guidance on protocol authorship, execution, and reporting.
  • Present validation strategies, progress, and results to client stakeholders and internal governance teams.

 

Necessary Expertise and Skills:

  • Deep knowledge of cGMP requirements and FDA/EMA expectations for process validation.
  • Hands-on experience authoring and executing validation studies a regulated manufacturing environment.
  • Experience developing cleaning validation programs, including toxicological limit-setting and analytical sampling methods.
  • Strong statistical and data analysis skills to support validation acceptance criteria and continued process verification.
  • Ability to manage multiple concurrent validation projects across client programs with competing priorities.
  • Excellent technical writing and cross-functional communication skills.

MINIMUM REQUIREMENTS

Minimum Qualifications For The Role:

  • Bachelor's degree in Engineering, Chemistry, Pharmaceutical Sciences, or related scientific discipline.
  • 5+ years of experience in validation, equipment qualification, or process engineering within a pharmaceutical, biotechnology, or CDMO environment.
  • Demonstrated experience authoring and executing manufacturing process and/or cleaning validation studies.
  • Working knowledge of statistical tools used in validation and continued process verification.
  • Experience supporting regulatory inspections or client audits related to validation activities.

 

Physical, Sensory, Cognitive & Neurological Demands:

  • Requires the ability to safely perform the physical movements necessary to carry out the essential functions of the role, including sitting, standing, walking, bending, reaching, lifting, pushing, pulling, and repetitive movements throughout the workday.
  • Occasional lifting up to 25–35 lbs 
  • Donning and working in PPE, including cleanroom gowning 
  • Manual dexterity for instruments and sampling tools
  • Visual acuity for reading technical documents and instrumentation 
  • Ability to distinguish color-coded labels and safety markings 
  • Hearing sufficient to detect alarms and verbal instructions 
  • Tactile sensitivity for equipment and sample handling
  • Sustained focus and attention to detail 
  • Strong analytical and problem-solving skills 
  • Ability to manage multiple concurrent priorities 
  • Sound judgment under regulatory scrutiny 
  • Clear verbal and written communication
  • Alertness in a safety-sensitive environment 
  • Ability to manage stress during audits and investigations 
  • Adequate coordination/reflexes for equipment operation 
  • Adaptability to shifting priorities


ProMed offers a generous benefits package including:

  • 401k with company match
  • Profit Sharing Program
  • Medical Insurance
  • Health Savings Account/Flexible Spending Account
  • Dental Insurance
  • Vision Insurance
  • Life Insurance
  • Paid Family Medical Leave and Long-Term Disability Insurance
  • Hospital Indemnity, Critical Illness, Accident, and Identity Theft Protection
  • Pet Insurance

ProMed does not discriminate in employment opportunities or practices on the basis of race, color, creed, religion, national origin, ancestry, age, sex, marital status, order of protection, disability, military status, sexual orientation, gender identity, pregnancy, public assistance, family status, unfavorable discharge from military service, genetic information or other segmenting factor protected by law, or local human rights commission activity.