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Process Engineer (GMP Manufacturing)

Ashtrix

Paris, Kentucky • Today

Full-time

USD 45.00 - 54.00 per hour

Senior Engineer, Process Validation

Danaher Corporation

Remote • Today

Full-time

USD 100,000.00 - 130,000.00 per year

Job Details

Skills

GMP
FOCUS
Engineering Support
Root Cause Analysis
Corrective And Preventive Action
Continuous Improvement
Process Optimization
Operational Efficiency
Performance Metrics
Change Control
Regulatory Compliance
Functional Requirements
Chemical Engineering
Mechanical Engineering
Industrial Engineering
Process Engineering
Pharmaceutics
Biotechnology
Manufacturing Operations
Process Improvement
Good Manufacturing Practice
Manufacturing
ROOT
Analytical Skill
Conflict Resolution
Problem Solving
Communication
Microsoft Excel
Microsoft PowerPoint

GMP
FOCUS
Engineering Support
Root Cause Analysis
Corrective And Preventive Action
Continuous Improvement
Process Optimization
Operational Efficiency
Performance Metrics
Change Control
Regulatory Compliance
Functional Requirements
Chemical Engineering
Mechanical Engineering
Industrial Engineering
Process Engineering
Pharmaceutics
Biotechnology
Manufacturing Operations
Process Improvement
Good Manufacturing Practice
Manufacturing
ROOT
Analytical Skill
Conflict Resolution
Problem Solving
Communication
Microsoft Excel
Microsoft PowerPoint

Summary

Pay Rate Low: 45 | Pay Rate High: 54
We are seeking a hands-on Process Engineer to support manufacturing operations within a highly regulated cGMP production environment. This role will focus on improving production performance, troubleshooting equipment and process issues, supporting capital projects, and driving continuous improvement initiatives.

Location: Paris, KY 40361
Pay: $45-$54/hr
Type: Contract-to-Hire
Fully Onsite
Key Responsibilities

Provide engineering support for manufacturing operations, equipment reliability, and process performance.
Investigate production issues, perform root cause analysis, and implement corrective and preventive actions (CAPA).
Lead continuous improvement initiatives focused on process optimization, yield improvement, waste reduction, and operational efficiency.
Support capital projects involving manufacturing equipment, facility upgrades, automation, and control systems.
Partner with Production, Quality, Safety, Maintenance, and Engineering teams to resolve operational challenges.
Develop and implement process performance metrics and monitoring tools.
Support validation, change control (MOC), and process qualification activities.
Work with vendors, contractors, and cross-functional stakeholders to implement process improvements.
Analyze manufacturing data and recommend solutions to improve equipment uptime and product quality.
Assist with new product introductions, technology transfers, and manufacturing scale-up activities.
Ensure compliance with cGMP, FDA, safety, environmental, and quality requirements.

Qualifications

Bachelor's Degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or a related Engineering discipline.
5+ years of Process Engineering experience within a pharmaceutical, chemical, biotechnology, or other regulated manufacturing environment.
Experience supporting manufacturing operations, process improvements, and troubleshooting production issues.
Knowledge of cGMP regulations and regulated manufacturing practices.
Experience performing root cause investigations and implementing corrective actions.
Strong analytical, problem-solving, and communication skills.
Proficiency with Microsoft Excel, Word, and PowerPoint.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

#LI-CS1
INDBH

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 10522794
Position Id: d6b9b2fdac1e3b6a374580ede04b63cc
Posted 1 day ago

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Job Details

Skills

GMP
FOCUS
Engineering Support
Root Cause Analysis
Corrective And Preventive Action
Continuous Improvement
Process Optimization
Operational Efficiency
Performance Metrics
Change Control
Regulatory Compliance
Functional Requirements
Chemical Engineering
Mechanical Engineering
Industrial Engineering
Process Engineering
Pharmaceutics
Biotechnology
Manufacturing Operations
Process Improvement
Good Manufacturing Practice
Manufacturing
ROOT
Analytical Skill
Conflict Resolution
Problem Solving
Communication
Microsoft Excel
Microsoft PowerPoint

GMP
FOCUS
Engineering Support
Root Cause Analysis
Corrective And Preventive Action
Continuous Improvement
Process Optimization
Operational Efficiency
Performance Metrics
Change Control
Regulatory Compliance
Functional Requirements
Chemical Engineering
Mechanical Engineering
Industrial Engineering
Process Engineering
Pharmaceutics
Biotechnology
Manufacturing Operations
Process Improvement
Good Manufacturing Practice
Manufacturing
ROOT
Analytical Skill
Conflict Resolution
Problem Solving
Communication
Microsoft Excel
Microsoft PowerPoint

Summary

Provide engineering support for manufacturing operations, equipment reliability, and process performance.
Investigate production issues, perform root cause analysis, and implement corrective and preventive actions (CAPA).
Lead continuous improvement initiatives focused on process optimization, yield improvement, waste reduction, and operational efficiency.
Support capital projects involving manufacturing equipment, facility upgrades, automation, and control systems.
Partner with Production, Quality, Safety, Maintenance, and Engineering teams to resolve operational challenges.
Develop and implement process performance metrics and monitoring tools.
Support validation, change control (MOC), and process qualification activities.
Work with vendors, contractors, and cross-functional stakeholders to implement process improvements.
Analyze manufacturing data and recommend solutions to improve equipment uptime and product quality.
Assist with new product introductions, technology transfers, and manufacturing scale-up activities.
Ensure compliance with cGMP, FDA, safety, environmental, and quality requirements.

Qualifications

Bachelor's Degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or a related Engineering discipline.
5+ years of Process Engineering experience within a pharmaceutical, chemical, biotechnology, or other regulated manufacturing environment.
Experience supporting manufacturing operations, process improvements, and troubleshooting production issues.
Knowledge of cGMP regulations and regulated manufacturing practices.
Experience performing root cause investigations and implementing corrective actions.
Strong analytical, problem-solving, and communication skills.
Proficiency with Microsoft Excel, Word, and PowerPoint.

Dice Id: 10522794
Position Id: d6b9b2fdac1e3b6a374580ede04b63cc
Posted 1 day ago

Fitment

Dice Job Match Score™

📊 Calculating match score...

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

Process Engineer

Paris, Kentucky

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Full-time

USD 53.00 per hour

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Yesterday

Easy Apply

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Process Engineer

Massachusetts

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USD 94,200.00 per year

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California

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