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Process Validation Manufacturing Engineer Jobs (NOW HIRING)

Foxconn WI

Manufacturing Engineer

Mount Pleasant, WI · On-site

$70K - $91K/yr

Manufacturing Engineer Department: Supporting Quality Employment Type: Full Time Location: SMC ... Conduct process validation and yield analysis * Troubleshoot and resolve process-related issues

Foxconn WI

Manufacturing Engineer

Mount Pleasant, WI · On-site

$70K - $91K/yr

Manufacturing Engineer Department: GL6 Maintenance Employment Type: Full Time Location: SMC ... Conduct process validation and yield analysis * Troubleshoot and resolve process-related issues

Danaher

Senior Engineer, Process Validation

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

Danaher

Senior Engineer, Process Validation

Sunnyvale, CA · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

FUJIFILM Biotechnologies

Position OverviewThe Senior Engineer or Scientist of Process Validation ensures that manufacturing processes meet the validation and regulatory requirements to ensure the process is robust and ...

Stark Pharma Solutions Inc

IL · On-site

Manufacturing Validation Engineer Location: Lake County, IL Duration: Long Term Position Overview ... Support Process Validation activities to ensure consistent manufacturing performance and product ...

Foxconn WI

Manufacturing Engineer

Mount Pleasant, WI · On-site

The Manufacturing Engineer will collaborate with design engineers to review PCB layouts, select ... Conduct process validation and yield analysis * Troubleshoot and resolve process-related issues

Danaher

Senior Engineer, Process Validation

Houston, TX · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

Danaher

Senior Engineer, Process Validation

Houston, TX · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

Danaher

Senior Engineer, Process Validation

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

Danaher

Senior Engineer, Process Validation

Boston, MA · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

Danaher

Senior Engineer, Process Validation

Raleigh, NC · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

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Process Validation Manufacturing Engineer information

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How much do process validation manufacturing engineer jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for process validation manufacturing engineer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $51.44 per hour, depending on experience, location, and employer.

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 are hiring for Process Validation Manufacturing Engineer jobs?

Cities with the most Process Validation Manufacturing Engineer job openings:

What states have the most Process Validation Manufacturing Engineer jobs?

States with the most job openings for Process Validation Manufacturing Engineer jobs include:

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

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

Infographic showing various Process Validation Manufacturing Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $82,237 per year, or $39.5 per hour.

Foundry Engineer - Casting Process (Medical Device Implants)

Raynham, MA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Posted 5 days ago

Job description

ABOUT COMPANY:

Stark Pharma Solutions Inc is a life sciences staffing and consulting firm supporting pharmaceutical, biotechnology and medical device organizations across the United States. We place quality, validation, manufacturing and regulatory professionals with companies building and scaling FDA-regulated operations. Our clients range from established manufacturers to early-stage sites standing up their first quality systems.

Foundry Engineer – Casting Process (Medical Device Implants)

JOB SUMMARY:

Our client, a medical device manufacturer in southeastern Massachusetts, is seeking a Foundry Engineer with hands-on foundry experience to support metal casting operations. This is a floor-facing role covering casting process support, tooling and gage activities, process validation and statistical analysis. Hands-on foundry experience is a mandatory requirement for this position. 

RESPONSIBILITIES:

  • Provide day-to-day manufacturing engineering support to foundry and casting operations
  • Support investment casting processes including wax injection, shell building, pouring, brazing and finishing
  • Troubleshoot casting defects and drive yield, scrap and process capability improvements
  • Author and execute process validation protocols (IQ/OQ/PQ) for casting equipment and processes
  • Support tooling, fixture and gage activities including design input, first article inspection and vendor coordination
  • Perform and interpret dimensional inspection using CMM and standard gaging methods; apply GD&T
  • Conduct statistical analysis using Minitab to support process characterization and validation
  • Partner with Quality, Maintenance and Operations on corrective actions, change control and documentation
  • Maintain manufacturing procedures, work instructions and equipment records

QUALIFICATIONS:

  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Metallurgy, Materials Science or a related technical discipline
  • Minimum 3 years of Mechanical or Manufacturing Engineering experience, with hands-on foundry experience required
  • Working knowledge of metals, casting, brazing and wax injection
  • Experience authoring and executing process validation protocols
  • Strong working knowledge of GD&T, CMM and gaging
  • Statistical analysis experience, ideally Minitab
  • Medical device or other regulated manufacturing experience preferred
  • NX CAD and Windchill experience preferred
  • Fixture and gage design, and wax injection tooling experience, are strong advantages
  • Must be able to work 100% onsite in Raynham, Massachusetts
  • Must be authorized to work in the United States without sponsorship, now or in the future
  • W2 employment only

HOW TO APPLY:

Please send your resume to deepika.b@starkpharma.com. In your email, please include your current location, your hands-on foundry or casting experience, your hourly rate expectation on W2, and your availability to start.