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Pharmaceutical Validation Manager Jobs in Michigan

BoehringerPRD

Description This position manages all equipment, process, systems and product related validation ... The position is critical to the compliance effort for both pharmaceuticals and vaccines and is ...

Neogen

Mechanical Validation Engineer

Lansing, MI · On-site

Other duties may be assigned by management. Education and/or Experience : * Minimum of a bachelor ... pharmaceutical environment. * OR an equivalent combination of education and experience will be ...

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Pharmaceutical Validation Manager information

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$41.4K

$91.9K

$139.9K

How much do pharmaceutical validation manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for pharmaceutical 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.

What does a pharmaceutical validation manager do?

A Pharmaceutical Validation Manager oversees the validation processes for equipment, systems, and processes within pharmaceutical manufacturing to ensure compliance with regulatory standards such as FDA and EMA guidelines. Their responsibilities include planning, coordinating, and documenting validation activities, managing teams, and ensuring that products meet quality and safety requirements. They play a key role in ensuring that all manufacturing procedures consistently produce products that meet predetermined quality criteria. Additionally, they may liaise with regulatory agencies during inspections and audits.

What are the key skills and qualifications needed to thrive as a pharmaceutical validation manager?

To thrive as a Pharmaceutical Validation Manager, you need a solid background in pharmaceutical sciences, engineering, or a related field, often supported by a relevant degree and experience in GMP-regulated environments. Familiarity with validation lifecycle documentation, risk assessment tools, and regulatory software systems such as TrackWise or Veeva Vault is typically required. Strong leadership, problem-solving, and communication skills set outstanding managers apart, enabling them to lead cross-functional teams and ensure compliance. These skills and qualities are crucial for maintaining product quality, meeting regulatory standards, and ensuring the safe and efficient production of pharmaceuticals.

What are some common challenges faced by pharmaceutical validation managers during regulatory inspections?

Pharmaceutical Validation Managers often encounter challenges during regulatory inspections, such as ensuring all validation documentation is complete, up-to-date, and compliant with current Good Manufacturing Practices (cGMP). Another challenge is demonstrating that all equipment and processes consistently operate within specified parameters, especially when inspectors request traceability and data integrity. Being able to quickly and accurately address auditor questions, provide supporting evidence, and manage unexpected findings requires thorough preparation and strong organizational skills.

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

The most popular types of Pharmaceutical Validation jobs in Michigan are:

What are popular job titles related to Pharmaceutical Validation Manager jobs in Michigan?

For Pharmaceutical Validation Manager jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Validation Manager jobs in Michigan look for?

The top searched job categories for Pharmaceutical Validation Manager jobs in Michigan are:

What cities in Michigan are hiring for Pharmaceutical Validation Manager jobs?

Cities in Michigan with the most Pharmaceutical Validation Manager job openings:

Pharmaceutical Validation Manager jobs near you
Infographic showing various Pharmaceutical Validation Manager job openings in Michigan as of August 2026, with employment types broken down into 82% Full Time, 13% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $91,879 per year, or $44.2 per hour.

Manager, Validation

BoehringerPRD

On-site

Full-time

Re-posted 25 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

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