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)
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Management and Manufacturing
Industries
Pharmaceutical Manufacturing
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