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Computer Validation Jobs in Michigan (NOW HIRING)

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

General Description The Manager of Validation leads the Commissioning, Qualification and Validation (CQV), and Computer System Validation (CSV) area. Ensures that all equipment, facilities, and ...

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

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

Computer literacy with strong knowledge of the MS Office Suite. Validation experience with knowledge of test and validation methods. Strong organizational and coordination skills with the ability to ...

Computer literacy with strong knowledge of the MS Office Suite. Validation experience with knowledge of test and validation methods. Strong organizational and coordination skills with the ability to ...

Validation Engineer Job Overview: The Validation Engineer is responsible for verifying after ... Manual dexterity for computer work. * Ability to communicate in an effective manner Work ...

Validation Engineer Job Overview: The Validation Engineer is responsible for verifying after ... Manual dexterity for computer work. * Ability to communicate in an effective manner Work ...

Advanced Driver Assistance Systems (ADAS) Verification and Validation Engineer to work with our ... Bachelor's degree in Computer Science, Computer Engineering, Electrical Engineering, or related ...

Required : • Bachelor's degree in engineering, Computer engineering, Computer or Information Science, or related degree. • 5 years of experience in software or systems validation, preferably in ...

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How much do computer validation jobs pay per hour?

As of May 29, 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 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 are popular job titles related to Computer Validation jobs in Michigan? For Computer Validation jobs in Michigan, the most frequently searched job titles are:
Infographic showing various Computer Validation job openings in Michigan as of May 2026, with employment types broken down into 70% Full Time, and 30% Contract. Highlights an 74% In-person, and 26% Remote job distribution, with an average salary of $98,475 per year, or $47.3 per hour.

Head of Validation

Biovire

Brighton, MI • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Posted 12 days ago


Job description

Head of Validation Brighton, Michigan
Biovire is advancing toward commercialization with a focus on operational excellence, compliance, and scalable GMP manufacturing systems. We are seeking a Manager of Validation to lead validation programs supporting equipment, facilities, utilities, and computerized systems within our regulated pharmaceutical manufacturing environment.
This is a highly visible leadership role responsible for ensuring validation programs support operational readiness, inspection readiness, and long-term manufacturing reliability as the organization continues to scale.
The Role
The Manager of Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight for validation strategy, execution, compliance, and lifecycle management of manufacturing systems and infrastructure.
This position partners closely with Quality, Manufacturing, Engineering, Maintenance, and cross-functional operational teams to ensure all systems remain compliant, qualified, and inspection-ready.
Key Responsibilities
  • Lead site validation programs supporting equipment, facilities, utilities, and computerized systems
  • Oversee commissioning, qualification, and validation activities in accordance with cGMP requirements
  • Manage and maintain Validation Master Plans and validation lifecycle documentation
  • Lead scheduling, planning, review, and execution of validation activities
  • Support transition of equipment and systems from Engineering to operational use
  • Partner cross-functionally with Quality, Manufacturing, Engineering, and Maintenance teams
  • Provide technical guidance for risk assessments, change controls, deviations, and investigations
  • Ensure timely completion of validation protocols, reports, traceability matrices, IQ/OQ documentation, and related deliverables
  • Support audit and inspection readiness activities
  • Lead and develop validation personnel while reinforcing a strong quality and compliance culture

What You Bring
  • Bachelor's degree in Engineering, Science, Computer Systems, or related technical field
  • 5+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments
  • Prior leadership experience within Validation, Engineering, CQV, or Quality functions
  • Strong understanding of cGMP, validation lifecycle management, and 21 CFR Part 11 requirements
  • Hands-on experience leading validation projects and technical documentation activities
  • Experience supporting manufacturing equipment, utilities, HVAC, automation systems, and/or computerized systems
  • Strong organizational, communication, and cross-functional collaboration skills

Why Join Biovire
  • Opportunity to shape and strengthen validation systems during organizational growth
  • High visibility and cross-functional leadership exposure
  • Collaborative and mission-driven GMP manufacturing environment
  • Direct impact supporting operational readiness and future commercialization
  • Company-paid medical, dental, vision, and life insurance
  • Paid Time Off supporting work-life balance

Come join us on our mission of manufacturing safe, high-quality products that improve and save lives.