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Process Validation Engineer Jobs in Michigan (NOW HIRING)

Neogen

Mechanical Validation Engineer

Lansing, MI

Neogen is looking to hire a Mechanical Validation Engineer who would be responsible for overseeing ... Strong written and verbal communications skills, excellent attention to detail, and process and ...

BTI Solutions

Telematics Validation Engineer

Troy, MI · On-site

Telematics Validation Engineer What We Can Offer A thoughtfully designed employee experience that ... Test case development processes and structured test case design * Defect and bug tracking systems

Expleo

Automotive Test & Validation Engineer

Troy, MI · On-site

... processes. * Oversee test script development using National Instruments LabVIEW and TestStand ... Minimum of 5 years of experience in test and validation engineering within the automotive or ...

Expleo

Automotive Test & Validation Engineer

Troy, MI · On-site

... processes. * Oversee test script development using National Instruments LabVIEW and TestStand ... Minimum of 5 years of experience in test and validation engineering within the automotive or ...

Expleo

Automotive Test & Validation Engineer

Troy, MI · On-site

... processes. * Oversee test script development using National Instruments LabVIEW and TestStand ... Minimum of 5 years of experience in test and validation engineering within the automotive or ...

Btisolutions

Telematics Validation Engineer

Troy, MI

Telematics Validation Engineer What We Can Offer A thoughtfully designed employee experience that ... Test case development processes and structured test case design * Defect and bug tracking systems

Pfizer, Inc.

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

$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 ...

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 ...

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Process Validation Engineer information

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How much do process validation engineer jobs pay per hour?

As of Aug 16, 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 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 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 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.

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 safe, effective, and compliant with industry regulations.

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 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 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:

What cities in Michigan are hiring for Process Validation Engineer jobs?

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 71% Full Time, and 29% Contract. Highlights an 100% In-person job distribution, with an average salary of $71,677 per year, or $34.5 per hour.

CQV/Process Engineer (New Grad)

Verista, Inc.

Kalamazoo, MI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 15 days ago

Job description

Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

CQV/Process Engineer Responsibilities:
CQV Engineers execute commissioning, qualification and validation projects involving new
or modified systems/equipment, processes, procedures, products, facilities, and utilities. In this role, validation
engineers support the validation and change lifecycles for client's systems in pharmaceutical and medical device
manufacturing, laboratory, IT, and packaging operations to meet timeline, budget, quality, regulatory compliance,
and client expectations.
Process Engineers support conceptual and detailed design, support in process scale-up, product development, process validation, and implementation of operational improvements that resolve manufacturing process investigations in pharmaceutical manufacturing environments. In this role, you may work in concert with the client or as part of a Verista team tasked in determining the root cause of manufacturing investigations or in designing/executing experiments and evaluating data in support of improvement and investigations. Additionally, engineers write technical reports in support of manufacturing process changes, optimizations, and regulatory filings (where required).
This is an entry level role. College graduates are encouraged to apply. We are looking for smart, hardworking team players to grow professionally into this role at our client site in Kalamazoo, MI.
Requirements
  • Bachelor's degree in chemical, biomedical/biochemical engineering, biological/chemical sciences or equivalent required
  • Must live in or relocate to the Kalamazoo MI area
  • Proficiency using PC and Microsoft Office tools
  • Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
  • Ability to work as part of a team
  • Ability to think critically and demonstrate troubleshooting and problem-solving skills
  • Excellent organizational and time management skills
  • Strong attention to detail
  • Possess excellent interpersonal, verbal, and written communication skills.
  • GxP and Good Documentation Practice training (may be completed at onboarding)
  • Process training (may be completed at onboarding)
  • Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes)
  • Basic skills with EXCEL and PowerPoint
  • Strong interpersonal skills and clear communication capabilities
  • Experience with and tolerance for high levels of challenge and change

Benefits
Why Choose Verista?
  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com

Apply