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Method Validation Jobs in Michigan (NOW HIRING)

Engineer, Process/Validation

Fraser, MI · On-site

$75K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Prepare protocols and reports for Installation Qualifications (IQ), and Operational Qualifications (OQ), Test Method Validations (TMV), and Performance Qualification (PQ). * Execute protocols to ...

Engineer, Process/Validation

Fraser, MI · On-site

$75K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Prepare protocols and reports for Installation Qualifications (IQ), and Operational Qualifications (OQ), Test Method Validations (TMV), and Performance Qualification (PQ). * Execute protocols to ...

Engineer, Process/Validation

Fraser, MI · On-site

$75K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Prepare protocols and reports for Installation Qualifications (IQ), and Operational Qualifications (OQ), Test Method Validations (TMV), and Performance Qualification (PQ). * Execute protocols to ...

New

Engineer, Process/Validation

Fraser, MI · Hybrid

$75K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Prepare protocols and reports for Installation Qualifications (IQ), and Operational Qualifications (OQ), Test Method Validations (TMV), and Performance Qualification (PQ). * Execute protocols to ...

Serve as technical resource for customer, federal, and/or YF test specifications and methods ... Manage a test schedule using validation database, and/or customer specific format. Understand ...

The Validation Engineer is responsible for developing validation test plans and timing schedules to ... High experience required to apply structured problem-solving methodologies (e.g., 8D) to determine ...

The Validation Engineer is responsible for developing validation test plans and timing schedules to ... solving methodologies (e.g., 8D) to determine whether issues are related to the product or test ...

The Validation Engineer is responsible for developing validation test plans and timing schedules to ... High experience required to apply structured problem-solving methodologies (e.g., 8D) to determine ...

The Validation Engineer is responsible for developing validation test plans and timing schedules to ... High experience required to apply structured problem-solving methodologies (e.g., 8D) to determine ...

You will build the tools, datasets, and evaluation methodologies that enable confident delivery of AI-driven automotive solutions. Key Responsibilities: * Design and implement validation frameworks ...

Validation Engineer - Powertrain

Plymouth, MI · On-site

$85K - $107K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Formulate clear validation methods and technical requirements; leverage engineering calculations and simulations to establish baseline test parameters. * Standardize Testing Procedures: Define highly ...

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Showing results 1-20

Method Validation information

What are the key skills and qualifications needed for method validation?

To excel in Method Validation, a strong background in analytical chemistry, laboratory techniques, and scientific data analysis is typically required, often supported by a degree in chemistry, biochemistry, or a related field. Familiarity with validation protocols, industry regulations (such as GLP, GMP, or ISO standards), and analytical instrumentation (e.g., HPLC, GC, MS) is essential. Strong attention to detail, problem-solving skills, and effective collaboration and documentation abilities help professionals thrive in this position. These skills are vital to ensure that laboratory methods are reliable, regulatory-compliant, and suitable for their intended purposes.

What is a method validation?

A Method Validation job involves assessing and verifying analytical methods to ensure they produce reliable, accurate, and reproducible results. Professionals in this role typically work in pharmaceutical, biotechnology, or chemical industries, following regulatory guidelines such as ICH, USP, or FDA requirements. Their responsibilities include designing validation protocols, performing experiments, analyzing data, and documenting results. Method validation ensures compliance with industry standards and guarantees product quality and safety.

What does a method validation do?

As a Method Validation professional, you will design, conduct, and document experiments to confirm that laboratory methods produce accurate and reproducible results under specified conditions. Typical daily tasks include preparing protocols, running validation samples, analyzing data, and preparing comprehensive validation reports for internal or regulatory review. You’ll work closely with scientists, quality assurance teams, and regulatory specialists to ensure compliance with industry standards. This collaborative environment provides opportunities to contribute to critical product development stages and to build expertise that supports career progression into quality management, regulatory affairs, or advanced analytical roles.

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

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

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

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

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

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

Infographic showing various Method Validation job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 5% Part Time, 2% Temporary, and 7% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution.

Engineer, Process/Validation

Getinge

Fraser, MI • On-site

$75K - $93K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 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 490 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