Description This position manages all equipment, process, systems and product related validation activities, except GXP related computerized systems for both Pharmaceuticals and Vaccines at the site
Description This position manages all equipment, process, systems and product related validation activities, except GXP related computerized systems for both Pharmaceuticals and Vaccines at the 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 ...
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 ...
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 ...
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 ...
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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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 ...
Enable Cross-Functional Alignment Manage the team of PVSE's to deliver GVBE (physical and virtual) by partnering with Chief Engineers, Program Engineering, Safety, and Quality to align validation and ...
Enable Cross-Functional Alignment Manage the team of PVSE's to deliver GVBE (physical and virtual) by partnering with Chief Engineers, Program Engineering, Safety, and Quality to align validation and ...
Head of 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 ...
Head of 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 ...
Head of 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 ...
Quick apply
Head of 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 ...
Enable Cross-Functional Alignment Manage the team of PVSE's to deliver GVBE (physical and virtual) by partnering with Chief Engineers, Program Engineering, Safety, and Quality to align validation and ...
Enable Cross-Functional Alignment Manage the team of PVSE's to deliver GVBE (physical and virtual) by partnering with Chief Engineers, Program Engineering, Safety, and Quality to align validation and ...
Head of 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 ...
Head of 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 ...
Enable Cross-Functional Alignment Manage the team of PVSE's to deliver GVBE (physical and virtual) by partnering with Chief Engineers, Program Engineering, Safety, and Quality to align validation and ...
Enable Cross-Functional Alignment Manage the team of PVSE's to deliver GVBE (physical and virtual) by partnering with Chief Engineers, Program Engineering, Safety, and Quality to align validation and ...
Emissions and OBD Validation Manager Hyundai America Technical Center, Inc. (HATCI), is the design, technology and engineering arm for all North American models of the Korea-based Hyundai Motor Group.
Emissions and OBD Validation Manager Hyundai America Technical Center, Inc. (HATCI), is the design, technology and engineering arm for all North American models of the Korea-based Hyundai Motor Group.
V&V Vehicle Testing Supervisor
Dearborn, MI · Hybrid
$115K - $218K/yr
Manage and develop validation teams (vehicle test, DV, and UAT) with clear roles, cadence, and performance expectations * Train teams on requirement-based testing, scenario driven UAT, and FAP/GPDS ...
V&V Vehicle Testing Supervisor
Dearborn, MI · Hybrid
$115K - $218K/yr
Manage and develop validation teams (vehicle test, DV, and UAT) with clear roles, cadence, and performance expectations * Train teams on requirement-based testing, scenario driven UAT, and FAP/GPDS ...
Project management capability, including planning validation activities, coordinating cross‑functional resources, and tracking progress. TRAVEL REQUIRED (%): lt;5% travel to meet customers and ...
Project management capability, including planning validation activities, coordinating cross‑functional resources, and tracking progress. TRAVEL REQUIRED (%): lt;5% travel to meet customers and ...
Project management capability, including planning validation activities, coordinating cross‑functional resources, and tracking progress. TRAVEL REQUIRED (%): gt;25% travel to meet customers and ...
Project management capability, including planning validation activities, coordinating cross‑functional resources, and tracking progress. TRAVEL REQUIRED (%): gt;25% travel to meet customers and ...
Validation Engineer
Grass Lake, MI · On-site
Manage the program Design Verification & Reporting (DVP&R) document. * Develop Verification & Validation plan inclusive of timing, test part allocation, and test part build. * Develop, manage, and ...
Validation Engineer
Grass Lake, MI · On-site
Manage the program Design Verification & Reporting (DVP&R) document. * Develop Verification & Validation plan inclusive of timing, test part allocation, and test part build. * Develop, manage, and ...
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 ...
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 ...
This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...
This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...
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 ...
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 ...
This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...
This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...
This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...
This diverse product portfolio requires a strong combination of technical expertise and interpersonal skills to effectively manage validation projects. Core responsibilities include requirements ...
Validation Manager information
See Michigan salary details
$41.4K - $50.4K
1% of jobs
$50.4K - $59.3K
4% of jobs
$66.7K is the 25th percentile. Wages below this are outliers.
$59.3K - $68.3K
24% of jobs
$68.3K - $77.2K
9% of jobs
The median wage is $83.7K / yr.
$77.2K - $86.2K
17% of jobs
$86.2K - $95.1K
8% of jobs
$95.1K - $104.1K
5% of jobs
$110.1K is the 75th percentile. Wages above this are outliers.
$104.1K - $113K
11% of jobs
$113K - $122K
8% of jobs
$122K - $130.9K
6% of jobs
$130.9K - $139.9K
8% of jobs
$41.4K
$91.9K
$139.9K
How much do validation manager jobs pay per year?
As of Jul 26, 2026, the average yearly pay for validation manager in Michigan is $91,879.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,900.00 and $115,000.00 per year, depending on experience, location, and employer.
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 role of a validation manager?
A validation manager oversees the process of ensuring that products, processes, or systems meet specified requirements and quality standards. They develop validation protocols, coordinate testing activities, and ensure compliance with industry regulations, often working with quality assurance teams and regulatory bodies.
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.
What is the 3 month rule for jobs?
The 3 month rule for a Validation Manager typically refers to the expectation that validation activities, such as process or equipment validation, should be completed within three months to ensure timely compliance and project progress. This timeframe helps maintain project schedules and regulatory adherence, especially in industries like pharmaceuticals or manufacturing where validation is critical. However, specific timelines can vary based on project scope and organizational policies.
What is the difference between Validation Manager vs Quality Assurance Specialist?
| Aspect | Validation Manager | Quality Assurance Specialist |
|---|---|---|
| Certifications | GxP, ISO, or industry-specific validation certifications | ISO, Six Sigma, or QA-related certifications |
| Work Environment | Regulated industries like pharmaceuticals, biotech, or medical devices | Manufacturing, software, or service industries |
| Primary Focus | Ensuring validation processes for equipment, systems, and processes meet standards | Monitoring 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.
What are Validation Managers?
Validation Managers are professionals responsible for overseeing and managing the validation processes within an organization, particularly in industries like pharmaceuticals, biotechnology, and manufacturing. Their main role is to ensure that products, equipment, and processes meet regulatory standards and operate consistently as intended. They coordinate validation activities, develop protocols, lead teams, and ensure compliance with quality and safety regulations. Validation Managers play a critical role in maintaining product quality, reducing risks, and ensuring that all procedures meet industry and governmental standards.
How to become a validation specialist?
To become a validation specialist, typically one needs a bachelor's degree in a scientific or technical field such as engineering, biology, or chemistry. Gaining experience in quality assurance, validation processes, and familiarity with regulatory standards like GMP or FDA guidelines is important, along with certifications such as CQE or CSQE. Strong analytical skills and knowledge of validation tools and documentation are also essential.
How much does a validation manager make?
A validation manager's average salary typically ranges from $80,000 to $130,000 annually, depending on experience, industry, and location. They often require knowledge of regulatory standards and validation tools, such as GxP or validation protocols, to ensure compliance and quality in manufacturing or pharmaceutical environments.
More about Validation Manager jobs
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 Manager jobs in Michigan? For Validation Manager jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Validation Manager jobs in Michigan look for? The top searched job categories for Validation Manager jobs in Michigan are:
What cities in Michigan are hiring for Validation Manager jobs? Cities in Michigan with the most Validation Manager job openings:
Other
Posted 17 days ago
Job description
Description
This position manages all equipment, process, systems and product related validation activities, except GXP related computerized systems for both Pharmaceuticals and Vaccines at the site . The position is critical to the compliance effort for both pharmaceuticals and vaccines and is responsible for assuring compliance of validated systems, process, equipment to current cGMP, FDA, EU, USDA and BI corporate requirements. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
Duties & Responsibilities
- Manages personnel, budgets and projects relating to systems, process, cleaning and equipment validation in GXP relevant areas such as Operations, R'D, Marketing at the facility.
- Maintains comprehensive electronic data base for tracking compliance and qualification status of all critical GXP relevant equipment, systems and processes.
- Identifies current trends in regulatory compliance for all validation procedures for equipment, systems and processes. Implements and updates the validation master plan (VMP) to assure compliance with regulatory and corporate requirements.
- Supports Product and Engineering Departments in the selection, review, acquisition, and upgrade of production equipment to assure future IQ/OQ/PQscan be performed on equipment sourced.
Requirements
- Bachelor degreefrom an accredited institutionin a scientific, bioengineering, or relevant discipline required, and a minimum of ten (10) years GMP validation experience in a GMP OR regulated manufacturing or similar environment.
- In lieu of a degree, a minimum of fifteen (15) years GMP validation experience in a GMP OR regulated manufacturing or similar environment.
- Experience must be inclusive of at least three (3) years in a leadership role leading people and/or projects.
- Shares technical and compliance knowledge horizontally and vertically across the site.
- Ability to plan, schedule, organize, prioritize, and coordinate project activities.
- Ability to function in a leadership role and within cross-functional teams.
- Strong knowledge of statistics, data bases, and quality principles.
- Ability to analyze validation and production data to assess compliance with GMP requirements and/or troubleshoot compliance problems.
- Must be self motivated and of high integrity.
Desired Skills, Experience and Abilities