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Validation Manager Jobs in Novi, MI (NOW HIRING)

Biovire

Manager, Validation

Brighton, MI · On-site

$100K - $120K/yr

Manager, Validation Brighton, Michigan Biovire is advancing toward commercialization with a focus on operational excellence, compliance, and scalable GMP manufacturing systems. We are seeking a ...

Biovire

Manager, Validation

Brighton, MI · On-site

Manager, Validation Brighton, Michigan Biovire is advancing toward commercialization with a focus on operational excellence, compliance, and scalable GMP manufacturing systems. We are seeking a ...

Biovire

Manager, Validation

Brighton, MI · On-site

$100K - $120K/yr

Manager, Validation Brighton, Michigan Biovire is advancing toward commercialization with a focus on operational excellence, compliance, and scalable GMP manufacturing systems. We are seeking a ...

Magna

Validation Engineer

Auburn Hills, MI · On-site

This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...

Magna

Validation Engineer

Southfield, MI

This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...

Magna

Validation Engineer

Auburn Hills, MI · On-site

This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...

Yanfeng

Validation Engineer

Novi, MI · On-site

Manage a test schedule using validation database, and/or customer specific format. Understand customer, federal, and/or YF specific requirements and test methods. Consistent use of validation process ...

Magna

Validation Engineer

Auburn Hills, MI

This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...

Rivian

Validation Engineer - Powertrain

Plymouth, MI · On-site

$85K - $107K/yr

Manage External & Supplier Labs: Support external validation efforts, including hands-on management at supplier facilities and safely operating Rivian driveline systems. * Teardown & Diagnostics:

Rivian

Validation Engineer - Powertrain

Plymouth, MI · On-site

$85K - $107K/yr

Manage External & Supplier Labs: Support external validation efforts, including hands-on management at supplier facilities and safely operating Rivian driveline systems. * Teardown & Diagnostics:

Rivian

Validation Engineer - Powertrain

Plymouth, MI

$85K - $107K/yr

Manage External & Supplier Labs: Support external validation efforts, including hands-on management at supplier facilities and safely operating Rivian driveline systems. * Teardown & Diagnostics:

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All JobsValidation JobsValidation Manager JobsValidation Manager Jobs in Novi, MI

Validation Manager information

See Novi, MI salary details

$44.6K

$98.9K

$150.6K

How much do validation manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for validation manager in Novi, MI is $98,900.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,900.00 and $123,800.00 per year, depending on experience, location, and employer.

What is a validation manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

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

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

How does a validation manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

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

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

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What job categories do people searching Validation Manager jobs in Novi, MI look for?

The top searched job categories for Validation Manager jobs in Novi, MI are:

What cities near Novi, MI are hiring for Validation Manager jobs?

Cities near Novi, MI with the most Validation Manager job openings:

Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Novi, MI as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $98,900 per year, or $47.5 per hour.

Manager, Validation

Biovire

Brighton, MI • On-site

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 2 days ago

Job description

Manager, 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, Validation, reporting to the VP, Engineering, 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, 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, Operations, Manufacturing, Engineering, Maintenance, and cross-functional operational teams to ensure all systems remain compliant, qualified, and inspection-ready.
Key Responsibilities
  • Lead enterprise validation programs supporting equipment, facilities, utilities, automation, and computerized systems across Biovire's GMP manufacturing operations.
  • Oversee commissioning, qualification, and the overall validation strategy and activities.
  • Partner with Operations and Quality to maintain the qualified state of manufacturing systems.
  • Support commercialization, technology transfer, process validation, and startup activities for new manufacturing processes and facilities.
  • Serve as Validation SME during FDA and regulatory inspections.
  • Lead lifecycle management of validation systems.
  • 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
  • Experience interacting with FDA or other regulatory agencies and supporting inspections.
  • Ability to communicate technical validation concepts during inspections.
  • 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