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Process Validation Engineer Jobs in Michigan (NOW HIRING)

Getinge

Engineer, Process/Validation

Fraser, MI · On-site

$75K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... engineers to develop & optimize processes required for new products. * Prepare protocols and reports for Installation Qualifications (IQ), and Operational Qualifications (OQ), Test Method Validations ...

Getinge

Engineer, Process/Validation

Fraser, MI · Hybrid

$75K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... engineers to develop & optimize processes required for new products. * Prepare protocols and reports for Installation Qualifications (IQ), and Operational Qualifications (OQ), Test Method Validations ...

Magna

Validation Engineer

Southfield, MI · On-site

Support quoting process, providing number of engineering hours and cost associated with testing In case of validation failures (Environmental/Electrical/EMC) document incidents in applicable tool.

Magna

Validation Engineer

Auburn Hills, MI · On-site

... processes. • Create and maintain accurate and detailed timing plans using Microsoft project ... Validation Engineer accountable for the actions taken by third party labs, from this get kickoff ...

Magna

Validation Engineer

Auburn Hills, MI · On-site

Support quoting process, providing number of engineering hours and cost associated with testing In case of validation failures (Environmental/Electrical/EMC) document incidents in applicable tool.

Yanfeng

Validation Engineer

Novi, MI · On-site

Consistent use of validation process protocols such as Issue Tracking and reporting, ED/DV/PV, DVP ... Bachelor's Degree (Engineering / technical). Experience: 3 Years suggested minimum experience in ...

Yanfeng Human Resources

Validation Engineer

Novi, MI · On-site

This position functions as a Validation Engineer within the Engineering Validation team. This team ... Support test report process by uploading files, loading test data and information, provide test ...

Neogen

Mechanical Validation Engineer

Lansing, MI

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

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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 15, 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.

Engineer, Process/Validation

Getinge

Fraser, MI • On-site

$75K - $93K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Getinge rating

9.3

Company rating: 9.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

12th of 489 rated machine equipment manufacturers

Job description

With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
Job Overview
Assist with the development & optimization of new manufacturing processes and equipment that will be or has been transferred to production for commercial release.
Job Responsibilities and Essential Duties:
  • Work with other engineers to develop & optimize processes required for new products.
  • Prepare protocols and reports for Installation Qualifications (IQ), and Operational Qualifications (OQ), Test Method Validations (TMV), and Performance Qualification (PQ).
  • Execute protocols to complete Installation Qualifications (IQ), and Operational Qualifications (OQ), Test Method Validations (TMV), and Performance Qualification (PQ).
  • Assist with preparation of process risk documentation (pFMEA).
  • Assist / Coordinate pilot production / pre-release manufacturing.
  • Work closely with Manufacturing to release new processes and equipment into production.
  • Work closely with Manufacturing to support new processes and equipment that have been recently released into production.
  • Assist with training efforts on new equipment and processes.
  • Assist with creating and implement required documentation including but not limited to; equipment history files, manufacturing procedures, test methods, BOM's, routings, etc.
  • Responsible for change orders (ECO/DCO's) required to release and/or update controlled items.
  • Maintain compliance to Quality System and regulations for new processes and equipment.
  • Assist in special projects as needed.
  • Contribute to team effort by accomplishing related duties as requested.

Required Knowledge, Skills and Abilities:
  • Problem solving / troubleshooting skills.
  • Excellent communication skills with the ability to prepare written reports.
  • Able to work in a cross functional team environment.
  • Computer skills including MS Office Suite (Word, Excel, etc.).
  • Experience with developing and optimizing new manufacturing processes preferred.
  • Experience with introducing new equipment / processes into production preferred.
  • Experience with process control & statistical analysis techniques preferred.

Minimum Requirements:
  • Bachelor's Degree in Engineering
  • Minimum 3 years experience medical device experience

Quality Requirements:
Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
  • Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function).
  • Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function).
  • Attend all required Quality & Compliance training at the specified interval.
  • Adopt the "Beyond Compliance Quality Culture" in the work environment; always meet and exceed requirements.

Environmental/Safety/Physical Work Conditions:
  • Ensures environmental consciousness and safe practices are exhibited in decisions.
  • Duties are performed in an office environment and within manufacturing spaces as required.

The physical demands described here are a representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Monday-Friday, 8:30am-5pm
$75,120-$93,900/annually + 4% STIP
#LI-LG1
#LI-Hybrid
About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
  • Health, Dental, and Vision insurance benefits
  • 401k plan with company match
  • Paid Time Off
  • Wellness initiative & Health Assistance Resources
  • Life Insurance
  • Short and Long Term Disability Benefits
  • Health and Dependent Care Flexible Spending Accounts
  • Commuter Benefits
  • Parental and Caregiver Leave
  • Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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About Getinge

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dr Wayne, NJ, US

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