Process Engineer (Pharma Manufacturing)

Dallas, TX, US • Posted 1 day ago • Updated 1 day ago
Contract Independent
Contract Corp To Corp
Contract W2
No Travel Required
On-site
Depends on Experience
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Fitment

Dice Job Match Score™

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Job Details

Skills

  • Equipment
  • pharmaceutical manufacturing
  • filling & packaging operations (bottle/tube)
  • root cause analysis
  • Chemical Engineering
  • Design of Experiments (DOE)

Summary

Job Title: Process Engineer (Pharma Manufacturing)

Location: Dallas, TX (Onsite – 75%+ required)

Role Overview

We are seeking a Lead Process Engineer with strong pharmaceutical manufacturing and quality experience, particularly in semi-solid and liquid/gel batch processes. This role requires a hands-on, equipment-focused professional who has worked directly in manufacturing environments—not just validation (C&Q).

The ideal candidate will have a Chemical Engineering background, strong process improvement expertise, and preferably a Six Sigma certification.

Key Responsibilities

  • Lead and execute Design of Experiments (DOE) to optimize manufacturing and packaging processes
  • Drive process improvement initiatives focusing on efficiency, quality, and reliability
  • Support and optimize semi-solid, liquid, and gel batch manufacturing processes
  • Work on filling and packaging operations (bottle/tube lines) within pharma environments
  • Perform root cause analysis for process deviations and implement corrective actions
  • Collaborate with Quality, Manufacturing, and Engineering teams
  • Act as a client-facing technical expert supporting on-site operations
  • Document process improvements, DOE results, and technical findings per industry standards

Required Qualifications

  • Bachelor’s or Master’s in Chemical Engineering
  • 5–10+ years of experience in pharmaceutical manufacturing/process engineering
  • Minimum 5 years of hands-on DOE experience
  • Strong experience in semi-solid, liquid, or gel manufacturing
  • Experience with filling & packaging operations (bottle/tube)
  • Strong expertise in root cause analysis & process optimization

Preferred Qualifications

  • Six Sigma (Green Belt/Black Belt) certification
  • Strong quality-focused background (Pharma preferred over cosmetics)
  • Experience working in regulated pharma environments (GMP)
  • Hands-on manufacturing experience (not just equipment validation/C&Q)
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: 91170485
  • Position Id: 115-44406-
  • Posted 1 day ago

Company Info

About Spadtek Solutions LLC

At Spadtek, we believe sustainable growth happens when talent works in harmony with technology. Success isn’t driven by tools alone—it’s built through collaboration and intelligent execution. We partner with organizations to design, build, and scale modern digital solutions. From strategy and consulting to engineering and transformation, our approach is hands-on and adaptive. We turn complexity into opportunity, helping businesses stay resilient in a fast-evolving digital world.

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