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Process Validation Manufacturing Engineer Jobs in Michigan

Work with other engineers to develop & optimize processes required for new products. * Prepare ... Work closely with Manufacturing to release new processes and equipment into production. * Work ...

Work with other engineers to develop & optimize processes required for new products. * Prepare ... Work closely with Manufacturing to release new processes and equipment into production. * Work ...

Work with other engineers to develop & optimize processes required for new products. * Prepare ... Work closely with Manufacturing to release new processes and equipment into production. * Work ...

Manufacturing Engineer

Romulus, MI · On-site

$70K - $90K/yr

Process Validation * Launch Readiness Activities Responsibilities include: * Lead APQP activities from product launch through production. * Prepare, review, and approve PPAP documentation. * Review ...

Manufacturing Engineer

Detroit, MI

$72K - $93K/yr

Generate and maintain clear, concise documentation including process instructions, validation ... manufacturing engineering for injection molding operations, with experience launching automated ...

Manufacturing Engineer

Lansing, MI · On-site

$74K - $95K/yr

Manufacturing Engineer Essential Duties and Responsibilities ... Design, develop, implement, and validate manufacturing processes, methods, tooling, equipment, and ...

Manufacturing Engineer

Lansing, MI · On-site

$74K - $95K/yr

Manufacturing Engineer Essential Duties and Responsibilities ... Design, develop, implement, and validate manufacturing processes, methods, tooling, equipment, and ...

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Showing results 1-20

Process Validation Manufacturing Engineer information

What is the difference between Process Validation Manufacturing Engineer vs Quality Control Analyst?

AspectProcess Validation Manufacturing EngineerQuality Control Analyst
Required CredentialsBachelor's in Engineering, Life Sciences, or related field; certifications like ASQ CQE or CSQEBachelor's in Chemistry, Biology, or related field; certifications like ASQ CQPA
Work EnvironmentManufacturing facilities, validation labs, production linesLaboratories, quality testing environments, production support
Employer & Industry UsagePharmaceutical, biotech, medical device manufacturingPharmaceutical, biotech, medical device industries

The Process Validation Manufacturing Engineer focuses on developing and executing validation protocols to ensure manufacturing processes meet quality standards. In contrast, the Quality Control Analyst primarily conducts testing and inspections to verify product quality. Both roles are essential in regulated industries like pharmaceuticals and biotech, often working together to ensure compliance and product safety.

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

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

Infographic showing various Process Validation Manufacturing Engineer job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 3% Contract, and 2% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Engineer, Process/Validation

Fraser, MI • Hybrid

Getinge
Medical Equipment and Supplies Manufacturing • 10K+ employees

$75K - $93K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 days ago


Getinge rating

9.3

Company rating: 9.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz


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