This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Seeking a Quality Validation Engineer with 6+ yrs experience in Pharma or Biotech MANUFACTURING ... Manufacturing process validation * Supporting validation execution and documentation Facility ...
New
Seeking a Quality Validation Engineer with 6+ yrs experience in Pharma or Biotech MANUFACTURING ... Manufacturing process validation * Supporting validation execution and documentation Facility ...
New
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Manufacturing Specialist-Process Engineer
New Albany, OH · On-site
$70K - $94K/yr
Process Validation Assist with the process validation and generation of process validation ... Or Bachelor's degree and 4 years in Engineering, Manufacturing, Packaging or Quality experience in ...
Manufacturing Specialist-Process Engineer
New Albany, OH · On-site
$70K - $94K/yr
Process Validation Assist with the process validation and generation of process validation ... Or Bachelor's degree and 4 years in Engineering, Manufacturing, Packaging or Quality experience in ...
The engineer collaborates with Manufacturing, Quality, Process Development, Engineering, and ... Process Validation & PPQ * Author and execute Process Performance Qualification (PPQ) protocols ...
The engineer collaborates with Manufacturing, Quality, Process Development, Engineering, and ... Process Validation & PPQ * Author and execute Process Performance Qualification (PPQ) protocols ...
Seeking a Quality Validation Engineer with 6+ yrs experience in Pharma or Biotech MANUFACTURING ... Manufacturing process validation * Supporting validation execution and documentation Facility ...
New
Seeking a Quality Validation Engineer with 6+ yrs experience in Pharma or Biotech MANUFACTURING ... Manufacturing process validation * Supporting validation execution and documentation Facility ...
New
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Integration (Process Validation) Engineer
Trevor, WI · On-site
$70K - $85K/yr
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Integration (Process Validation) Engineer
Trevor, WI · On-site
$70K - $85K/yr
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Seeking a Quality Validation Engineer with 6+ yrs experience in Pharma or Biotech MANUFACTURING ... Manufacturing process validation * Supporting validation execution and documentation Facility ...
New
Quick apply
Seeking a Quality Validation Engineer with 6+ yrs experience in Pharma or Biotech MANUFACTURING ... Manufacturing process validation * Supporting validation execution and documentation Facility ...
New
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Process/Validation Engineer
Littleton, CO · On-site
$76K - $107K/yr
... Validation/Process Engineer to join the Application Innovation Group (AIG). The AIG team's mission ... manufacturing solutions for 3D Systems, our customers, and society as a whole. By leveraging ...
Process/Validation Engineer
Littleton, CO · On-site
$76K - $107K/yr
... Validation/Process Engineer to join the Application Innovation Group (AIG). The AIG team's mission ... manufacturing solutions for 3D Systems, our customers, and society as a whole. By leveraging ...
Process/Validation Engineer
Littleton, CO · On-site
$76K - $107K/yr
... Validation/Process Engineer to join the Application Innovation Group (AIG). The AIG team's mission ... manufacturing solutions for 3D Systems, our customers, and society as a whole. By leveraging ...
Process/Validation Engineer
Littleton, CO · On-site
$76K - $107K/yr
... Validation/Process Engineer to join the Application Innovation Group (AIG). The AIG team's mission ... manufacturing solutions for 3D Systems, our customers, and society as a whole. By leveraging ...
Process/Validation Engineer
$76K - $107K/yr
... Validation/Process Engineer to join the Application Innovation Group (AIG). The AIG team's mission ... manufacturing solutions for 3D Systems, our customers, and society as a whole. By leveraging ...
Process/Validation Engineer
$76K - $107K/yr
... Validation/Process Engineer to join the Application Innovation Group (AIG). The AIG team's mission ... manufacturing solutions for 3D Systems, our customers, and society as a whole. By leveraging ...
The engineer collaborates with Manufacturing, Quality, Process Development, Engineering, and ... Process Validation & PPQ * Author and execute Process Performance Qualification (PPQ) protocols ...
The engineer collaborates with Manufacturing, Quality, Process Development, Engineering, and ... Process Validation & PPQ * Author and execute Process Performance Qualification (PPQ) protocols ...
Integration (Process Validation) Engineer
Trevor, WI · On-site
$70K - $85K/yr
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Quick apply
Integration (Process Validation) Engineer
Trevor, WI · On-site
$70K - $85K/yr
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Integration (Process Validation) Engineer
$70K - $85K/yr
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
Quick apply
Integration (Process Validation) Engineer
$70K - $85K/yr
This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements ...
The engineer collaborates with Manufacturing, Quality, Process Development, Engineering, and ... Role Responsibilities Process Validation & PPQ * Author and execute Process Performance ...
The engineer collaborates with Manufacturing, Quality, Process Development, Engineering, and ... Role Responsibilities Process Validation & PPQ * Author and execute Process Performance ...
While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging.
While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging.
Engineer, Process/Validation
Fraser, MI · Hybrid
$75K - $93K/yr
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 ...
Engineer, Process/Validation
Fraser, MI · Hybrid
$75K - $93K/yr
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 ...
Process Validation Manufacturing Engineer information
See salary details
$7.93 - $13.51
5% of jobs
$13.51 - $19.08
2% of jobs
$23.08 is the 25th percentile. Wages below this are outliers.
$19.08 - $24.65
24% of jobs
$24.65 - $30.22
13% of jobs
$30.22 - $35.80
1% of jobs
The median wage is $38.02 / hr.
$35.80 - $41.37
11% of jobs
$41.37 - $46.94
14% of jobs
$49.03 is the 75th percentile. Wages above this are outliers.
$46.94 - $52.51
13% of jobs
$52.51 - $58.09
4% of jobs
$58.09 - $63.66
5% of jobs
$63.66 - $69.23
7% of jobs
$7
$39
$69
How much do process validation manufacturing engineer jobs pay per hour?
What is the difference between Process Validation Manufacturing Engineer vs Quality Control Analyst?
| Aspect | Process Validation Manufacturing Engineer | Quality Control Analyst |
|---|---|---|
| Required Credentials | Bachelor's in Engineering, Life Sciences, or related field; certifications like ASQ CQE or CSQE | Bachelor's in Chemistry, Biology, or related field; certifications like ASQ CQPA |
| Work Environment | Manufacturing facilities, validation labs, production lines | Laboratories, quality testing environments, production support |
| Employer & Industry Usage | Pharmaceutical, biotech, medical device manufacturing | Pharmaceutical, 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:

Integration (Process Validation) Engineer
Trevor, WI • On-site
Other
Re-posted 23 days ago
Job description
About Vonco Products
Sourced by ZipRecruiter
Industry
Plastics packaging film and sheet (including laminated) manufacturing
Company size
51 - 200 Employees
Headquarters location
Trevor, WI, US
Year founded
1955