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Process Validation Engineer Jobs in Michigan (NOW HIRING)

Delphi Technologies

Senior Validation Engineer

Troy, MI · On-site

$90 - $130/hr

Become the Subject Matter Expert on the Test Incident Report Process (TIR) * This role is based in ... engineering field. * Strong Knowledge of validation requirements in automotive components

Pfizer

Senior Validation Engineer

Rochester, MI · On-site

$82K - $137K/yr

Use Your Power for Purpose The Rochester Senior Validation Engineer is responsible for planning ... Carryout process capability analysis on all commercial processes on a periodic basis. Identify ...

Ford Motor Company

Virtual Validation Engineer

Dearborn, MI · Hybrid

$115K - $192K/yr

The engineer in this role will develop and maintain electronic control unit (ECU) simulations at ... In the United States, if you need a reasonable accommodation for the online application process due ...

Ford Motor Company

Virtual Validation Engineer

Dearborn, MI · Hybrid

$115K - $192K/yr

The engineer in this role will develop and maintain electronic control unit (ECU) simulations at ... In the United States, if you need a reasonable accommodation for the online application process due ...

Pfizer

Senior Validation Engineer

Rochester, MI · On-site

$82K - $137K/yr

Guide the writing, review, and approval of validation process documents and technical reports ... Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering ...

Pfizer

Senior Validation Engineer

Rochester, MI · On-site

$83 - $138/hr

Guide the writing, review, and approval of validation process documents and technical reports ... Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering ...

Ford Motor Company

Virtual Validation Engineer

Dearborn, MI · On-site +1

$115K - $192K/yr

The engineer in this role will develop and maintain electronic control unit (ECU) simulations at ... In the United States, if you need a reasonable accommodation for the online application process due ...

Stellantis

SW Validation Engineer

Auburn Hills, MI · On-site

Bachelor's degree in Computer Science, Computer Engineering, Electrical Engineering, or a related ... Experience working within an Agile/Scrum software development process. * Experience working with ...

Ford

Virtual Validation Engineer

Dearborn, MI · On-site

$99.60 - $192.90/hr

The engineer in this role will develop and maintain electronic control unit (ECU) simulations at ... In the United States, if you need a reasonable accommodation for the online application process due ...

Stellantis

SW Validation Engineer

Auburn Hills, MI

Bachelor's degree in Computer Science, Computer Engineering, Electrical Engineering, or a related ... Experience working within an Agile/Scrum software development process. * Experience working with ...

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Process Validation Engineer information

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How much do process validation engineer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for process validation engineer in Michigan is $34.46, according to ZipRecruiter salary data. Most workers in this role earn between $20.10 and $44.86 per hour, depending on experience, location, and employer.

What is a process validation engineer?

Process Validation Engineers are professionals responsible for ensuring that manufacturing processes consistently produce products that meet predetermined quality standards. They design, execute, and document validation protocols to verify that equipment, systems, and processes operate effectively and efficiently. These engineers play a crucial role in regulated industries such as pharmaceuticals, biotechnology, and medical devices, where compliance with industry standards and regulatory requirements is essential. Their work helps to minimize risks, ensure product safety, and maintain regulatory compliance.

What are the key skills and qualifications needed to thrive as a process validation engineer?

To thrive as a Process Validation Engineer, you need a solid background in engineering or life sciences, a thorough understanding of validation protocols, and knowledge of industry regulations such as GMP. Experience with validation software, statistical analysis tools, and familiarity with regulatory documentation systems are typically required. Strong analytical thinking, attention to detail, and effective communication skills help you resolve issues and coordinate cross-functional teams. These skills and qualities are essential to ensure processes are compliant, efficient, and produce high-quality, safe products.

What are some common challenges faced by process validation engineers during product scale-up?

Process Validation Engineers often encounter challenges when scaling up products from development to full-scale manufacturing. These can include ensuring process consistency, managing variations in equipment or raw materials, and troubleshooting unexpected deviations that may not have surfaced during small-scale trials. Effective communication with cross-functional teams—such as quality assurance, production, and R&D—is essential to quickly address issues and maintain compliance with regulatory requirements. Being proactive and detail-oriented helps navigate these complexities and ensures successful validation outcomes.

What is the difference between Process Validation Engineer vs Quality Assurance Engineer?

AspectProcess Validation EngineerQuality Assurance Engineer
Primary FocusValidating manufacturing processes to ensure product quality and complianceDeveloping and implementing quality systems and procedures to prevent defects
CertificationsGMP, ISO, Six Sigma often preferredISO, Six Sigma, CQE certifications common
Work EnvironmentManufacturing, pharmaceutical, biotech facilitiesQuality departments across various industries
Key ResponsibilitiesProcess validation, protocol development, troubleshootingAudits, quality audits, process improvements

While both roles aim to ensure product quality, the Process Validation Engineer primarily focuses on validating manufacturing processes, whereas the Quality Assurance Engineer oversees overall quality systems and compliance. Both roles often collaborate but serve distinct functions within the quality management framework.

Do process validation engineers make good money?

Process validation engineers typically earn competitive salaries that vary by industry, experience, and location. They often have specialized skills in quality assurance, regulatory compliance, and validation tools, which can lead to higher compensation levels. Overall, the role is considered well-paying within manufacturing, pharmaceutical, and biotech sectors.

What does a process validation engineer do?

A process validation engineer is responsible for developing, executing, and documenting validation protocols to ensure manufacturing processes meet quality and regulatory standards. They analyze process data, identify risks, and implement improvements using tools like statistical analysis and validation software. Their work helps ensure products are consistently produced to specifications and comply with industry regulations.

What are popular job titles related to Process Validation Engineer jobs in Michigan?

For Process Validation Engineer jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Process Validation Engineer jobs in Michigan look for?

The top searched job categories for Process Validation Engineer jobs in Michigan are:

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Cities in Michigan with the most Process Validation Engineer job openings:

What are popular job titles related to Process Validation Engineer jobs in MI?

For Process Validation Engineer jobs in MI, the most frequently searched job titles are:

Process Validation Engineer jobs near you
Infographic showing various Process Validation Engineer job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 23% Part Time, 2% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $71,677 per year, or $34.5 per hour.

Qualification Validation Engineer

TOWER LABORATORIES LTD.

Montague, MI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Join a team where your expertise can spark real innovation by shaping a future of wellness. We’re seeking a skilled chemist ready to transform ideas into impactful solutions.

Tower Laboratories is a leading effervescent product manufacturer in the U.S. We develop and manufacture over-the-counter medications, prescription pharmaceuticals, nutritional supplements, soft drink tablets and other consumer products on a contract basis. We are continually expanding our effervescent product base and currently have several new and interesting products in the research and development phase right now. We are a family owned company and have been in business for over 40 years. 

Tower Labs' production environment is clean and temperature and humidity controlled. Uniforms provided free of charge.

We are not offering relocation assistance for this position.

www.towerlabs.com

POSITION SUMMARY:

This position is responsible for initiating, conducting and implementing engineering evaluations, new equipment or processes installations (in coordination with Staff Engineer and Facilities Manager), design and general improvements associated with the manufacturing processes at Tower Laboratories. These activities support operational requirements to maximize operating effectiveness as well as fulfilling the need to document manufacturing systems and satisfy regulatory requirements. 

ESSENTIAL FUNCTIONS:

    • Write and perform qualifications and validations for products and processes
    • Write and execute IQ, OQ and PQ on manufacturing equipment
    • Prepare annual reports to assess product trends, submit recommendations to management by summarizing and analyzing the processes, develops action plan to correct the issues highlighted in the evaluations
    • Writes specifications and procedures
    • Interfaces with R&D in new product development by working with department on scale-ups and new product development
    • Conducts internal as well as external audits as needed
    • Reviews existing manufacturing processes and leads a team of representatives from a number of departments in improving the processes
    • Interfaces with customers on the transfer and implementation of manufacturing process
    • Conducts related training when needed
    • Performs evaluations, conducts research and initiates compatibility studies on alternate materials
    • Assists in the writing and reviewing of new Batch Records
    • Interfaces on technical issues between the Manufacturing and Technical Departments
    • Performs all work in accordance with established Safety, cGMP and company procedures
    • Other related responsibilities as assigned other duties as requested

ESSENTIAL SKILLS and EXPERIENCE:

  • Minimum 2 years experience in chemical engineering
  • Computer literate with spreadsheet, databases and CAD
  • Familiarity with SPC & IE analysis techniques
  • Strong problem analysis and problem resolution at both a strategic and a functional level
  • Strong verbal and written communication skills 
  • Ability to organize and manage multiple projects
  • Ability to communicate effectively with team members and other plant personnel

EDUCATION:

Technical engineering degree required; Bachelor’s degree in an engineering discipline preferred

BENEFITS:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Employee assistance program
  • Health insurance
  • Life insurance
  • Paid time off
  • Tuition reimbursement
  • Vision insurance
  • Prescription safety lens reimbursement 
  • ANSI - approved safety shoe reimbursement

SCHEDULE:

  • Monday to Friday
  • Overtime
  • Full time
  • On Site 

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.