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Process Engineering Supervisor Jobs in Nebraska (NOW HIRING)

Provide process engineering support acrossproduction processes. * Troubleshoot process and equipment issues directly with operators, mechanics, supervisors, and technical teams. * Lead or support ...

Provide process engineering support across production processes. * Troubleshoot process and equipment issues directly with operators, mechanics, supervisors, and technical teams. * Lead or support ...

Provide process engineering support across production processes. * Troubleshoot process and equipment issues directly with operators, mechanics, supervisors, and technical teams. * Lead or support ...

Work closely with shift supervisors in communicating process changes from shift to shift. * Ensure ... Mechanical or Chemical Engineering preferred. * 3-5 years of industrial process experience ...

New

Work closely with shift supervisors in communicating process changes from shift to shift. * Ensure ... Mechanical or Chemical Engineering preferred. * 3-5 years of industrial process experience ...

New

Process Engineer

South Sioux City, NE · On-site

$84K - $112K/yr

Responsible for day-to-day production, maintenance, and engineering support and troubleshooting to ... Ability to train and coach others to improve performance, including supporting supervisor training ...

Indirectly supervises all resources assigned to project teams. Ensure compliance with BD quality ... A Bachelors Degree in an engineering discipline or equivalent experience. Minimum Experience:

Indirectly supervises all resources assigned to project teams. Ensure compliance with BD quality ... A Bachelors Degree in an engineering discipline or equivalent experience. Minimum Experience:

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Process Engineering Supervisor information

What cities in Nebraska are hiring for Process Engineering Supervisor jobs?

Cities in Nebraska with the most Process Engineering Supervisor job openings:

Infographic showing various Process Engineering Supervisor job openings in Nebraska as of June 2026, with employment types broken down into 79% Full Time, 18% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Process Engineer - 1099 or W-2

Omaha, NE • On-site

GMP Pros
Pharmaceutical and Medicine Manufacturing • 11 - 50 employees

$85/hr

Contractor

Re-posted 14 days ago


Job description

  • 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?


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 BioTech 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


Essential Duties:

  • Provide process engineering support acrossproduction 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, andexecution-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.
  • Own Project Engineering scope across the full project lifecycle - maturing URS/specification quality in partnership with the site team, vendor identification and assessment, and equipment installation activities (FAT/SAT, IOQ/PQ) - bridging process and project engineering rather than working in a silo.
  • Build the business case for process and capital improvements with quantifiable results (cost savings, capacity gains, risk reduction) to support site funding decisions.


Requirements:

  • 10-15 years of process engineering experience in an FDA-regulated or similarly controlled manufacturing environment.
  • Demonstrated change leadership - proven ability to earn trust on the floor, guide operators and technical teams through process and organizational change, and sustain momentum without forcing it.
  • DemonstratedSME-level knowledge andexperience supportingBiologicalprocesses, 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 thevalidationlifecycle.
  • Working knowledge of project engineering principals and proven experienceowning capital/small-cap project scope end-to-end - budget, schedule, design, and construction oversight - while staying grounded in the process itself.
  • 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.
  • Experience developing the capability of others - mentoring engineers, co-ops, or technicians and elevating team performance over time.


Pre-EmploymentRequirements:

  • Pass and maintain pre-employment/contract background check and safety certification, including but not limited to outstanding professional references.
  • Subjecttomotorvehiclereportreview.
  • Maintainvaliddriver'slicenseandendorsementsasrequiredperposition.
  • 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-sitefull-timeat theClientfacility.
  • 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.

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About GMP Pros

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

Omaha, NE, US

Year founded

2013