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Computer Validation Jobs in Michigan (NOW HIRING)

Yanfeng

Validation Engineer

Novi, MI

This position functions as a Validation Engineer within the Engineering Validation team. This team ... Constantly Use Hands/Fingers (Operate computer, printer, phone): Constantly Thank you for your ...

Yanfeng Human Resources

Validation Engineer

Novi, MI · On-site

This position functions as a Validation Engineer within the Engineering Validation team. This team ... Constantly Use Hands/Fingers (Operate computer, printer, phone): Constantly About Us Thank you for ...

Biovire

Head of Validation

Brighton, MI

The Role The Manager, Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight ...

Biovire

Head of Validation

Brighton, MI · On-site

The Role The Manager, Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight ...

Biovire

Head of Validation

Brighton, MI · On-site

The Role The Manager, Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight ...

Ford Motor Company

HIL Validation Engineer

Allen Park, MI · Hybrid

$85K - $192K/yr

Bachelor's Degree in Electrical Engineering, Computer Engineering, Computer Science or equivalent 5+ Years of experience in automotive software development or validations. 5+ Years of experience in ...

Ford Motor Company

Software Validation Engineer

Dearborn, MI · On-site +1

$123K - $164K/yr

Master's degree or foreign equivalent in Electrical Engineering, Computer Science, Software Engineering or related field and 5 years of experience in the job offered or a related software validation ...

Pfizer

Senior Validation Engineer

Rochester, MI

$82K - $137K/yr

Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems * Experience with sterile products and medical devices

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Computer Validation information

See Michigan salary details

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$47

$75

How much do computer validation jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for computer validation in Michigan is $47.34, according to ZipRecruiter salary data. Most workers in this role earn between $36.44 and $56.15 per hour, depending on experience, location, and employer.

What is the salary of SoC validation engineer?

The salary of a SoC validation engineer typically ranges from $80,000 to $130,000 annually, depending on experience, location, and company size. Entry-level positions may start lower, while experienced engineers with specialized skills in hardware description languages and verification tools can earn higher salaries.

How to become a validation specialist?

To become a validation specialist, typically one needs a bachelor's degree in life sciences, engineering, or a related field, along with experience in quality assurance or manufacturing. Certification in validation or Good Manufacturing Practices (GMP) can enhance job prospects. Skills in documentation, attention to detail, and knowledge of validation tools and protocols are essential for success in this role.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What is the salary of a CSV engineer?

A CSV (Computer System Validation) engineer's salary typically ranges from $70,000 to $120,000 annually, depending on experience, location, and certifications. Senior roles or those with specialized skills in validation tools and regulatory compliance may earn higher salaries.

Is computer system validation a good field?

Computer validation professionals ensure that computer systems in regulated industries meet quality and compliance standards, often requiring knowledge of GxP regulations and validation tools. The field offers steady demand, especially in pharmaceuticals and biotech, with opportunities for certification and career growth. It is suitable for those with technical skills and attention to detail interested in quality assurance and regulatory compliance.
What are popular job titles related to Computer Validation jobs in Michigan? For Computer Validation jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in Michigan look for? The top searched job categories for Computer Validation jobs in Michigan are:
Computer Validation jobs near you
Infographic showing various Computer Validation job openings in Michigan as of July 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $98,475 per year, or $47.3 per hour.

Validation Engineer

Corium Innovations

Grand Rapids, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 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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