1

Computer System Validation Jobs in Michigan (NOW HIRING)

Validation Engineer

Grand Rapids, MI · On-site

$85 - $125/hr

... computer systems. This includes successfully working with other departments, contract resources, and customers/vendors (as applicable) to plan, develop, maintain and execute validation and ...

We are seeking a Senior AI Validation Engineer to design and implement testing strategies ... system integration disciplines. Basic Qualifications: * Bachelor's degree in computer science ...

We are seeking a Senior AI Validation Engineer to design and implement testing strategies ... system integration disciplines. Basic Qualifications: * Bachelor's degree in computer science ...

The Validation Engineer reports directly to the Manager of Validation. The role is responsible for ... This role ensures all systems operate within regulations to ensure the production of quality ...

New

Senior Validation Engineer

Rochester, MI · On-site

$82.70 - $137.90/hr

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

New

System Validation test benches: closed loop HIL, reinjection HIL, system integration test bench ... Experience in Image Processing, Video pipeline and Computer vision. * Experience with requirements ...

New

Showing results 21-40

Computer System Validation information

See Michigan salary details

$9

$47

$75

How much do computer system validation jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for computer system 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 a computer system validation?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in computer system validation, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in computer system validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It offers opportunities for professionals with skills in validation protocols, regulatory requirements, and tools like GxP and 21 CFR Part 11. The field provides steady employment, career growth, and the chance to work on critical quality assurance processes.

What are the most commonly searched types of Computer System Validation jobs in Michigan?

The most popular types of Computer System Validation jobs in Michigan are:

What are popular job titles related to Computer System Validation jobs in Michigan?

For Computer System Validation jobs in Michigan, the most frequently searched job titles are:

What cities in Michigan are hiring for Computer System Validation jobs?

Cities in Michigan with the most Computer System Validation job openings:

Infographic showing various Computer System Validation job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $98,475 per year, or $47.3 per hour.

Validation Engineer

Corium Innovations

Grand Rapids, MI • On-site

$85 - $125/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 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.

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.
  • Excellent interpersonal and communication skills, both written and verbal.
  • 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.
#J-18808-Ljbffr