Process Engineer

Paris, KY, US • Posted 1 day ago • Updated 3 minutes ago
Contract W2
Contract Independent
12 Months
No Travel Required
On-site
$50 - $58/hr
Fitment

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Job Details

Skills

  • Process Engineering
  • Chemical Manufacturing
  • cGMP-Regulated Manufacturing
  • Pharmaceutical Manufacturing
  • 5+ Years Process Engineering Experience
  • 2+ Years Chemical Manufacturing Experience
  • Bachelor’s Degree in Chemical Engineering or Related Engineering Field
  • Root Cause Analysis
  • CAPA
  • MOC
  • Process Improvement
  • DMAIC
  • Lean Manufacturing
  • SPC
  • Equipment Troubleshooting
  • Process Control
  • Production Support
  • Capital Projects
  • FDA/cGMP Compliance
  • Strong Communication & Presentation Skills

Summary

Tranzeal is an industry leading global Business Transformation Service Provider offering specific consulting services as well as prepackaged, industry specific solutions and services to companies around the world. Our Consulting Services are dedicated to helping our clients maximize their investments in IT and the overall effectiveness and efficiency of the business. Tranzeal s deep industry experience makes us the partner of choice for a growing number of Fortune 1000 companies, midsize enterprises and small businesses worldwide.

We are currently looking for ''HR Shared Service Specialist'' to support one of our clients with the following skills:

Requirement:

Now Hiring: Process Engineer
Location: Paris, KY 40361
Pay Rate: $50–$58/hr on W2 (Depends on experience)
Schedule: Monday–Friday, 8:00 AM–5:00 PM
Occasional 6:00 AM starts and overtime as needed
Duration: 12 months (Temp-to-Possible-Hire)

We are looking for an experienced Process Engineer to support manufacturing operations within a pharmaceutical, chemical, or highly regulated cGMP manufacturing environment.

Key Requirements:


Bachelor’s Degree in Chemical Engineering or related Engineering field
5–8 years of Process Engineering experience
Minimum 2 years of chemical manufacturing experience
Strong experience in cGMP-regulated manufacturing
Pharmaceutical solutions, solvents, or similar manufacturing experience strongly preferred
Experience supporting capital projects, manufacturing equipment, and control systems/software
Strong knowledge of Lean Manufacturing, DMAIC, SPC, Kaizen, 5S and continuous improvement
Experience with root cause analysis, CAPA, MOC and validation
Knowledge of FDA, cGMP, ISO, OSHA and applicable regulatory requirements
Strong troubleshooting skills related to equipment downtime, process reliability and production efficiency
Excellent communication, presentation and cross-functional collaboration skills
Strong Microsoft Office skills, especially Excel, Word and PowerPoint

What You’ll Do:


The Process Engineer will provide hands-on engineering leadership and technical support to manufacturing operations, drive process improvements, improve equipment uptime and throughput, reduce process variability and waste, support capital projects, and partner with Quality, Safety, Production, Engineering, Maintenance, R&T and external vendors.
Candidates should be comfortable working directly in a manufacturing environment and leading both day-to-day operational support and larger process improvement initiatives.

 



Interested candidates: Please send your updated resumes to

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: 10439527
  • Position Id: 9054223
  • Posted 1 day ago
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