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Validation Jobs in Michigan (NOW HIRING)

Biovire

Head of Validation

Brighton, MI · On-site

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 ...

Slate Auto

Telematics Validation Engineer

Troy, MI · On-site

WHO WE ARE LOOKING FOR A detail-oriented Validation Engineer with approximately 5 years of experience in automotive software or systems validation. This position is responsible for verification and ...

Slate Auto

Telematics Validation Engineer

Troy, MI · On-site

They are seeking a detail-oriented Validation Engineer responsible for the verification and validation of vehicle telematics systems, including mobile application interfaces and vehicle communication ...

Recar

Telematics Validation Engineer

Troy, MI · On-site

WHO WE ARE LOOKING FOR A detail-oriented Validation Engineer with approximately 5 years of experience in automotive software or systems validation. This position is responsible for verification and ...

Truck Hero

Manager - Systems Validation

Ann Arbor, MI · On-site

POSITION SUMMARY The Manager of Systems Validation Engineering is responsible for the testing and validation function for RealTruck. This position will be responsible for leading the corporate ...

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Validation information

See Michigan salary details

$19

$45

$68

How much do validation jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for validation in Michigan is $45.32, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $55.10 per hour, depending on experience, location, and employer.

What is a validation job?

A validation job involves verifying that products, processes, or systems meet specified standards and requirements. It often includes tasks such as testing, documentation, and compliance checks, especially in industries like pharmaceuticals, manufacturing, and technology. Skills in quality assurance, attention to detail, and familiarity with validation protocols are typically required.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

What is the 3 month rule for jobs?

In validation roles, the 3 month rule often refers to a probationary period during which an employee's performance and fit for the position are assessed. This period typically allows employers to evaluate skills, adherence to procedures, and reliability before confirming permanent employment or considering further training. It is common for companies to set this timeframe to ensure quality and compliance in validation processes.

What jobs pay $10,000 a month without a degree?

Validation roles typically do not pay $10,000 a month without specialized skills or experience. High-paying jobs that can reach this level without a degree often include sales, real estate, or certain entrepreneurial ventures, but they usually require strong skills, certifications, or a proven track record. Most roles with such income levels rely on performance-based compensation rather than formal education alone.

What engineers make $500,000?

Senior engineers in specialized fields such as software, petroleum, or aerospace engineering can earn $500,000 or more annually, often through a combination of base salary, bonuses, and stock options. High-level roles typically require extensive experience, advanced skills, and sometimes professional certifications or advanced degrees.

What are the key skills and qualifications needed to thrive as a Validation Engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What are validation jobs?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Michigan? The most popular types of Validation jobs in Michigan are:
What are popular job titles related to Validation jobs in Michigan? For Validation jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Validation jobs in Michigan look for? The top searched job categories for Validation jobs in Michigan are:
What cities in Michigan are hiring for Validation jobs? Cities in Michigan with the most Validation job openings:
Validation jobs near you

Head of Validation

Biovire

Brighton, MI • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Posted 29 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.

Apply