Process Engineer
Job in
Paris, Bourbon County, Kentucky, 40361, USA
Listed on 2026-07-08
Listing for:
Astrix
Full Time
position Listed on 2026-07-08
Job specializations:
-
Manufacturing / Production
Quality Engineering, Lean Manufacturing / Six Sigma, Validation Engineer -
Engineering
Process Engineer, Quality Engineering, Lean Manufacturing / Six Sigma, Validation Engineer
Job Description & How to Apply Below
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.
- 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.
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