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Senior Validation Engineer Jobs in Minnesota (NOW HIRING)

Senior Quality Engineer

Arden Hills, MN · On-site

$89K - $121K/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 ...

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 ...

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 ...

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 ...

Senior Quality Engineer

New Hope, MN

$91K - $124K/yr

This Sr Quality Engineer will also work cross-functionally contributing to development and manufacturing engineering qualification and validation activities. They will support Operations, Sales, and ...

Senior Mechanical Engineer

Minneapolis, MN · On-site

$110 - $150/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Role Overview As a Senior Mechanical Engineer , you will lead the design, optimization, and validation of advanced mobile mechanical systems used in demanding industrial and oil & gas applications.

Sr. Engineer - Water Resources

Hopkins, MN · On-site

$125K - $175K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Senior Engineer shall be capable of independently managing projects and collaboratively ... A valid driver's license is required or the ability to obtain one. * This position will require the ...

Sr. Engineer - Water Resources

Minnetonka, MN · On-site

$106K - $146K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Senior Engineer shall be capable of independently managing projects and collaboratively ... A valid driver's license is required or the ability to obtain one. * This position will require the ...

Senior Quoting Engineer

Big Lake, MN · On-site

$90 - $115/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This is a senior-level individual contributor role with no direct supervisory responsibility. Key ... Validate routing and process assumptions with Engineering and Operations * Estimate cost impact of ...

Senior Quoting Engineer

Big Lake, MN · On-site

$90K - $115K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This is a senior-level individual contributor role with no direct supervisory responsibility. Key ... Validate routing and process assumptions with Engineering and Operations * Estimate cost impact of ...

Senior Design Engineer

Jackson, MN

$85K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

May direct work of other design or validation engineers, technicians, and contractors on assigned projects. Works closely with new product development teams globally that require rubber track systems ...

Senior Design Engineer

Jackson, MN

$85K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

May direct work of other design or validation engineers, technicians, and contractors on assigned projects. Works closely with new product development teams globally that require rubber track systems ...

Engineer Senior - Lead

Duluth, MN · On-site

$110K - $137K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Exempt Engineer Senior - Lead $110,000 - $137,000 | Will report in person Ready to shape Minnesota ... Must possess and maintain a valid driver's license and be willing to travel to project sites.

Senior Design Engineer

Jackson, MN · On-site

$85K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

May direct work of other design or validation engineers, technicians, and contractors on assigned projects. Works closely with new product development teams globally that require rubber track systems ...

Sr. Quality Engineer

Chaska, MN · On-site

$120K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

JOB SUMMARY The Senior Quality Engineer is a member of the Quality Assurance team that will ... This Senior role is responsible for providing support for design verification and validation ...

Sr. Quality Engineer

Chaska, MN · On-site

$120K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

JOB SUMMARY The Senior Quality Engineer is a member of the Quality Assurance team that will ... This Senior role is responsible for providing support for design verification and validation ...

Senior Data Engineer

Minneapolis, MN · On-site

$110K - $150K/yr

Senior Data Engineer Location: Minneapolis, MN or Madison, WI Duration: 6+ Months Note :Only W2 no ... Microsoft Fabric * Strong understanding of data quality, validation, and production support ...

Senior Systems Engineer

Eagan, MN · Remote

$106K - $145K/yr

Senior Systems Engineer - Agile Team Systems Engineering Leidos is seeking Senior Systems Engineers ... define, refine, and validate system capabilities. You will ensure that operational needs ...

Senior Manufacturing Engineer

Faribault, MN · On-site

$104K - $123K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Senior Manufacturing Engineer is responsible for identifying, developing, validating, and deploying manufacturing technologies, automation solutions, and standardized processes that improve ...

Showing results 21-40

Senior Validation Engineer information

See Minnesota salary details

$34

$63

$96

How much do senior validation engineer jobs pay per hour?

As of Aug 13, 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 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 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 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 cities in Minnesota are hiring for Senior Validation Engineer jobs? Cities in Minnesota with the most Senior Validation Engineer job openings:
Infographic showing various Senior Validation Engineer job openings in Minnesota as of August 2026, with employment types broken down into 93% Full Time, 2% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $131,953 per year, or $63.4 per hour.

Senior Quality Engineer

Boston Scientific

Arden Hills, MN • On-site

$89K - $121K/yr

Full-time

Posted 21 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

33rd of 538 rated manufacturers


Job description

Additional Location(s):  N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions.           

About the role:

Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work.

Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.

The Packaging, Sterilization and Men's Health team within Arden Hills Operations is seeking a Senior Quality Engineer to develop, implement and maintain quality engineering systems, methodologies and practices that ensure compliance with Boston Scientific, customer and regulatory requirements.

As a key quality representative, you will provide technical leadership and partner across functions to drive quality initiatives that support operational excellence, product quality and business objectives. You will play a critical role in process validation, risk management, process controls and continuous improvement efforts, ensuring products consistently meet internal and external requirements throughout the product life cycle. Working in a collaborative environment, you will lead quality engineering projects, mentor technical team members and apply data-driven problem-solving approaches to identify, resolve and prevent quality issues while strengthening manufacturing processes and quality system effectiveness.

Work model, sponsorship, relocation:

At Boston Scientific, we value collaboration and synergy. This role follows an onsite work model requiring employees to work from our Arden Hills, Minnesota, location. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.

 

Your responsibilities will include:

  • Select appropriate techniques for problem-solving and make sound, consistent engineering and quality assurance recommendations.
  • Read and interpret technical drawings, procedures and protocols.
  • Exercise independent authority to make decisions related to product quality, including the disposition of nonconforming product.
  • Identify manufacturing process defects, including scrap, nonconforming material and customer complaints, by dispositioning nonconforming material, assisting with root cause identification and supporting corrective and preventive actions. Partner with process owners to define product holds and document release criteria as needed.
  • Participate in customer complaint investigations for assigned manufacturing areas.
  • Support the execution and investigation of corrective and preventive actions (CAPAs), nonconforming events, failure mode investigations and related quality system activities.
  • Demonstrate and promote the highest standards of quality engineering discipline and technical rigor.
  • Serve as a quality systems resource by promoting compliance with Quality System Regulation (QSR), ISO standards and applicable medical device regulations while escalating critical quality decisions to Quality Engineering leadership when appropriate.
  • Apply advanced validation engineering expertise while ensuring compliance with applicable regulatory requirements.
  • Review and approve operational, test and validation data to establish technical specifications and performance standards for new or modified products and processes.
  • Champion continuous improvement and innovation from a quality perspective throughout the product life cycle, from supplier qualification through customer satisfaction.
  • Provide technical guidance and mentorship to Quality Engineers, Associate Quality Engineers, technicians and inspection personnel.
  • Partner with Environmental Health and Safety to identify significant environmental impacts and support goals and objectives that improve environmental performance.
  • Collaborate with suppliers, manufacturing, engineering and cross-functional partners to resolve quality issues and drive operational excellence.
  • Support internal quality audits and maintain audit readiness.

 

Qualifications:

Required qualifications:

  • Bachelor's degree or higher, preferably in an engineering discipline.
  • Minimum of 9 years' experience in operations quality.
  • Strong understanding of quality operations fundamentals, regulatory requirements and quality systems.
  • Experience working in regulated manufacturing environments.
  • Experience with product risk assessment.
  • Experience performing root cause analysis and implementing corrective and preventive actions.
  • Experience with CAPA, nonconforming event and failure mode investigations.
  • Experience with validation engineering and process validation.
  • Knowledge of Quality System Regulation (QSR), ISO standards and medical device regulations.
  • Experience reviewing operational, test and validation data to establish technical specifications and performance standards.
  • Strong analytical and decision-making skills with the ability to solve complex quality issues.
  • Excellent communication and cross-functional collaboration skills.
  • Experience conducting customer complaint investigations.

Preferred qualifications:

  • Experience in the medical device industry.
  • Experience using data analysis to identify trends, determine root causes and implement effective solutions.
  • Demonstrated ability to influence stakeholders and lead quality initiatives across cross-functional teams.
  • Experience mentoring technical team members and providing engineering guidance.

Requisition ID: 631913 

Minimum Salary: $ 85000 

Maximum Salary: $ 161500 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more atwww.bostonscientific.comand follow us onLinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status.  Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment.  Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.   As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company's policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.  


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