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Senior Validation Engineer Jobs in Michigan (NOW HIRING)

The Pivot Group

Validation Engineer - Walker Area

Walker, MI · On-site

$81K - $121K/yr

... Senior Validation Engineer, Lead Validation Engineer, Principal Validation Engineer Why The Pivot Group Network The Pivot Group Network was founded by manufacturing professionals who've been on both ...

Rivian

Sr. Durability Validation Engineer

Plymouth, MI

$111K - $138K/yr

Bachelor's degree in mechanical engineering, automotive engineering, materials engineering, or a ... Must have a valid driver's license in the state of residence that you will be driving/operating a ...

Rivian

Sr. Durability Validation Engineer

Plymouth, MI · On-site

$111K - $138K/yr

Bachelor's degree in mechanical engineering, automotive engineering, materials engineering, or a ... Must have a valid driver's license in the state of residence that you will be driving/operating a ...

Rivian

Sr. Durability Validation Engineer

Plymouth, MI · On-site

$111K - $138K/yr

Bachelor's degree in mechanical engineering, automotive engineering, materials engineering, or a ... Must have a valid driver's license in the state of residence that you will be driving/operating a ...

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All JobsValidation Engineer JobsSenior Validation Engineer JobsSenior Validation Engineer Jobs in Michigan

Senior Validation Engineer information

See Michigan salary details

$30

$56

$86

How much do senior validation engineer jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for senior validation engineer in Michigan is $56.46, according to ZipRecruiter salary data. Most workers in this role earn between $45.05 and $64.13 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 Michigan? The most popular types of Validation Engineer jobs in Michigan are:
What are popular job titles related to Senior Validation Engineer jobs in Michigan? For Senior Validation Engineer jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Senior Validation Engineer jobs in Michigan look for? The top searched job categories for Senior Validation Engineer jobs in Michigan are:
What cities in Michigan are hiring for Senior Validation Engineer jobs? Cities in Michigan with the most Senior Validation Engineer job openings:
What are popular job titles related to Senior Validation Engineer jobs in MI? For Senior Validation Engineer jobs in MI, the most frequently searched job titles are:
Senior Validation Engineer jobs near you
Infographic showing various Senior Validation Engineer job openings in Michigan as of July 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $117,427 per year, or $56.5 per hour.

Validation Engineer

Corium Innovations

Grand Rapids, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

Corium Innovations is seeking a Validation Engineer II/Sr. Validation Engineer who will be responsible for the maintenance and execution of the site validation programs including equipment, facilities, utilities, lab instrumentation and computer systems.  This includes successfully working with other departments, contract resources, and customers/vendors (as applicable) to plan, develop, maintain and execute validation and qualification activities.  This position will also be involved with site audit activities, investigations, change management evaluation and qualified utility ownership. The Sr. Validation Engineer is responsible for performing appropriate validation/qualification activities (IQ/OQ/PQ) and other system support activities to meet department, site and corporate objectives. This position involves the review and reporting of data, annual review and routine qualification/verification activities required for all systems.
Your most Innovative career move is here!
At Corium Innovations, we’ve led the way in innovating drug delivery technologies for millions of patients whose GI systems just can’t tolerate pills, who can’t remember to take their meds as directed, or who have needle-phobia. This is only the beginning! There’s so much more to deliver, and we need YOU to do it!
Our Purpose is to create, develop and manufacture innovative healthcare products for partners that deliver superior value to patients.
Our Goal is to be the best-in-class specialty CDMO through the use of innovative technologies and superior execution.
Our Company Values are core to our positive and people-centric culture which inspires all of us to come to work every day on behalf of our people, our partners, our customers, and our patients. Through our four core values, we put people first and create opportunities to make each day better than the last.
  • Celebrate Individuals: We’re looking for talent who will celebrate the uniqueness of each of our team members by encouraging everyone to bring their authentic self to work.
  • Successful Together: We believe we’re better together, so we prioritize teamwork as we work to achieve our shared vision knowing each one of us has an important role to play.
  • Embrace Innovation: We embrace new challenges and opportunities while encouraging creative thinking and innovative solutions to best meet the needs of our people and our partners.
  • Pride in Ownership: We take pride in owning our progress and successes, feeling empowered to pursue our growth to reach our full potential. And we hope you will too!
Responsibilities:
  • Development of validation or qualification deliverables, performing testing, verification, calibration, and routine maintenance of equipment, facilities, utilities, lab instruments and computer systems.
  • Develop and maintain procedures for qualification utilizing known industry best practices.
  • Utility and functional area reporting.
  • Quality system interaction (investigation, CAPA, change control)
  • Asset Management System ownership and maintenance
  • Continuous Improvement and other special projects in the Engineering Services functional area.
Qualifications:
  • Bachelor’s degree in a STEM field.
  • 5+ Years’ experience in the pharmaceutical industry.
  • Strong knowledge of FDA/cGMP/ISO requirements.
  • Knowledge of GMP Quality Systems and working knowledge of regulatory requirements.
  • Previous hands-on experience with equipment, facilities, utilities, lab instruments and computer system qualification (IQ/OQ/PQ), requirements documents, impact assessments, and summary reports preferred.
  • Previous hands-on experience with lab instrumentation and calibration, including but not limited to HPLC/UHPLC, GC, Dissolution Baths.
  • Cleanroom and qualified utility monitoring and qualification experience preferred.
  • Demonstrated analytical skill/problem solving skills. 
  • Must have good organizational skills, able to multi-task, and be capable of adjusting to changing priorities.
  • Self-starter
  • Excellent interpersonal and communication skills, both written and verbal.
Benefits:
  • Highly competitive benefits program including medical, dental, vision, flexible spending accounts, life insurance, disability insurance, and employee assistance program.
  • 401(k) retirement savings account with a company match and immediate vesting.
  • 12 paid holidays.
  • Competitive paid vacation plan plus ~1 additional week of paid time off for our annual holiday shutdown.

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