×
Register Here to Apply for Jobs or Post Jobs. X

Process Engineer - or W

Job in Omaha, Douglas County, Nebraska, 68197, USA
Listing for: GMP Pros®
Full Time position
Listed on 2026-05-18
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Process Engineer - 1099 or W-2

Job Overview

We are looking for a seasoned, floor-oriented Process Engineer who can support both manufacturing and packaging. This person must be able to troubleshoot in real time with operators, stabilize processes, support validation/change-related activities, understand and support project engineering initiatives (project lifecycle) and bring strong experience in Bio Tech environments.

Be part of an exciting start-up that supports the world’s leading pharmaceutical, biotech, food, and animal health companies. Get the best of both worlds. Gain experience at a company that leads projects for global pharmaceutical companies while enjoying the flexibility, energy, and personal attention that can only be found working in a small, close-knit company.

APPLICANTS MUST HAVE PRIOR EXPERIENCE IN BIOTECH, PHARMACEUTICAL, OR ANIMAL HEALTH INDUSTRIES TO BE CONSIDERED.

Qualities
  • Do you find satisfaction in building trust before driving change?
  • Do you enjoy helping teams evolve at a pace they can sustain, not just accelerate?
  • Can you guide others through change without forcing it?
  • Are you comfortable working in environments where relationships matter as much as results?
  • Do you take pride in mentoring others and raising the capability of a team over time?
Essential Duties
  • Provide process engineering support across production processes.
  • Troubleshoot process and equipment issues directly with operators, mechanics, supervisors, and technical teams.
  • Lead or support investigations, root cause analysis, and corrective actions tied to deviations, recurring losses, or process failures.
  • Support validation-related activities, continued process verification, process monitoring, and change implementation as needed.
  • Partner with QA, QC, Maintenance, Engineering, and Operations to keep processes controlled, reliable, and execution-ready.
  • Support line trials, startup/ramp-up activities, and technical improvements tied to throughput, quality, reliability, and waste reduction.
  • Help connect upstream manufacturing conditions with downstream packaging performance so issues are solved at the actual source.
  • Support Project Engineering across the project lifecycle from URS/specification development to vendor identification and assessment, to equipment installation activities (FAT/SAT, IOPQ).
Requirements
  • 7–10+ years of process engineering experience in an FDA-regulated or similarly controlled manufacturing environment.
  • Demonstrated SME-level knowledge and experience supporting Biological processes, including aseptic filling.
  • Strong troubleshooting capability in live production environments.
  • Experience with deviations, investigations, root cause analysis, change control, and technical process improvement.
  • Demonstrated experience with the validation lifecycle.
  • Working knowledge of project engineering principals and proven experience across the project lifecycle.
  • Comfort working on-site full time and moving between multiple production areas throughout the day.
  • Ability to work directly with operators and site teams in a practical, hands‑on support role.
  • Bachelor’s degree in Chemical, Mechanical, Industrial, or related Engineering discipline.
Strongly Preferred
  • Experience with line trials, technology transfer, startup support, or new product introduction.
  • Exposure to continued process verification, FMEA, Lean, TPM, centerlining, or reliability improvement methods.
  • Experience using plant systems or reporting tools such as SAP, MES, or Power BI.
Pre-Employment Requirements
  • Pass and maintain pre-employment/contract background check and safety certification, including but not limited to outstanding professional references.
  • Subject to motor vehicle report review.
  • Maintain valid driver’s license and endorsements as required per position.
  • Pass pre-employment/contract physical, medical evaluation, and drug screen due to the safety-sensitive nature of this position.
  • Successfully complete and maintain any required safety certification and testing on an annual basis.
Work Environment Expectations
  • This role is expected to be on-site full-time at the Client facility.
  • The individual must be comfortable entering various manufacturing and packaging areas as needed to support operators and troubleshoot issues.
  • This is a hands‑on site support role, not a primarily remote or conference-room-based engineering assignment.
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary