Gmppros

Gmppros

Industrial Engineer - 1099

Waco, Texas · Full-time

Sponsorship not specifiedDetected 21 days ago
C++Data VisualizationSAPProcess ImprovementGMPMedical Devices

About the role

  • Conduct equipment and process readiness assessments: inventory line count, machine count, mechanical and electronic adjustment points, changeover formats, and available performance data (OEE, downtime, changeover time).
  • Conduct operator and maintenance interviews and on-floor observations to capture machine quirks, setup practices, undocumented knowledge, and current-state culture.
  • Establish and facilitate centerline review cadences (weekly/bi-weekly) with client operations, maintenance, and engineering teams, covering OEE, changeover data, downtime trends, and centerline change review.

Responsibilities

  • analyze current changeover procedures, identify waste and variability, and implement standard changeover SOPs with measurable improvement.
  • Support identification and development of client-side centerline champions to sustain the program after GMP Pros' engagement concludes.
  • Partner with QA, Maintenance, Operations, and Engineering to keep packaging lines controlled, compliant, and execution-ready in accordance with client GMP requirements.
  • GMP Pros is seeking a Packaging Engineer with direct centerlining expertise to support client packaging operations through our phased centerlining engagement model.
  • They should bring Lean or Six Sigma credentials and the ability to engage operators, maintenance, and supervisors at the floor level to deliver durable results for our clients.
  • 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.

Requirements

  • 5-10+ years of hands-on packaging engineering experience in a regulated or GMP-controlled manufacturing environment.
  • Experience designing and executing DOEs in a production packaging environment, including defining success criteria, managing data collection, and translating results into documented centerline settings.
  • Bachelor's degree in Engineering (Mechanical, Industrial, Chemical, Packaging, or related discipline).
  • Experience supporting or leading centerlining for multiple equipment types across a full packaging line - e.g., fillers, cappers, labelers, cartoners, blister lines, case packers, or serialization equipment.
  • Familiarity with OEE analysis and the ability to tie centerline and changeover data to line-level OEE trends.
  • Experience with packaging line TPM programs, PM review and alignment to OEM recommendations, or reliability improvement work tied to packaging equipment.
  • This person must have direct, hands-on experience building centerlines, running DOEs, reducing changeover, and driving the cultural and operational disciplines that make centerlining stick.
  • Experience with statistical tools such as Minitab or JMP for capability studies, control charting, and DOE analysis.

Nice to have

  • Familiarity with GMP expectations for documentation, change control, and deviation management in a packaging context.

Compensation

  • Successfully complete and maintain any required safety certification and testing on an annual basis.

Benefits

  • Be part of an exciting start-up that supports the world's leading pharmaceutical, biotech, food, and animal health companies.
  • Experience in a life sciences packaging environment - pharmaceutical, consumer health, OTC, or medical device packaging strongly preferred.

This listing is sourced directly from Gmppros's careers page and normalized into a canonical job model.