Packaging Process Engineer

Katalyst HealthCares and Life Sciences

$90K — $120K *
US-AnywhereRemote in Durham, NC
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in related engineering discipline (Mechanical, Manufacturing, Chemical, etc.)
  • 5+ years of experience in pharmaceutical manufacturing, focusing on packaging
  • Experience with automated packaging equipment in a GMP environment
  • Strong understanding of packaging equipment validation and qualification processes
  • Knowledge of FDA and EU GMP regulations and best practices
  • Proven experience in process improvements and manufacturing optimization
  • Excellent communication and cross-functional collaboration skills

Responsibilities

  • Provide technical leadership for packaging operations in pharmaceutical manufacturing expansion
  • Support equipment implementation, commissioning, qualification, and optimization
  • Collaborate with Manufacturing, Quality Assurance, Validation, Automation, Maintenance, and Project Engineering
  • Ensure equipment reliability and regulatory compliance in packaging operations
  • Drive efficient production performance through continuous improvement initiatives

Benefits

  • Project-specific consulting role with significant industry impact
  • Opportunity to work on large-scale pharmaceutical manufacturing expansion
  • Collaboration with diverse teams in an innovative environment
  • Exposure to advanced pharmaceutical packaging technologies
  • Opportunity for professional development and skill enhancement in a leading industry sector
Full Job Description
Responsibilities:

  • Seeking an experienced Packaging Process Engineer to support a large-scale pharmaceutical manufacturing expansion. This consultant will provide technical leadership for pharmaceutical packaging operations, supporting equipment implementation, commissioning, qualification, process optimization, and commercial manufacturing readiness.
  • Working closely with Manufacturing, Quality Assurance, Validation, Automation, Maintenance, and Project Engineering, this individual will optimize packaging operations while ensuring equipment reliability, regulatory compliance, and efficient production performance. The successful candidate will have experience supporting automated pharmaceutical packaging lines from startup through commercial operations.

Requirements:
  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Chemical Engineering, Industrial Engineering, Packaging Engineering, or a related engineering discipline.
  • 5+ years of pharmaceutical manufacturing experience, with direct experience supporting packaging operations.
  • Experience supporting automated packaging equipment within a GMP-regulated environment.
  • Strong understanding of packaging equipment validation, manufacturing startup, and process qualification.
  • Knowledge of FDA cGMP regulations, EU GMP requirements, and pharmaceutical packaging best practices.
  • Experience supporting process improvements, equipment reliability initiatives, and manufacturing optimization.
  • Excellent troubleshooting, technical writing, communication, and cross-functional collaboration skills.

Preferred Qualifications:
  • Experience with serialization, aggregation, and track-and-trace systems.
  • Experience supporting packaging of sterile injectable products, cartridges, syringes, or combination products.
  • Familiarity with MES, SAP, TrackWise, or other manufacturing execution and quality systems.
  • Lean Manufacturing and Six Sigma experience is preferred.

Most Important Skills Needed:
  • Pharmaceutical packaging process engineering experience
  • utomated packaging line experience
  • Cartoners, labelers, case packers, palletizers, and packaging equipment
  • Equipment startup, commissioning, and qualification (FAT, SAT, IQ, OQ, PQ)
  • Packaging process optimization and continuous improvement
  • Manufacturing troubleshooting and root cause investigations
  • GMP-regulated pharmaceutical manufacturing
  • Cross-functional collaboration with Manufacturing, Validation, Automation, and Quality
  • Technical documentation, engineering studies, and protocol development
  • Experience supporting commercial manufacturing operations.

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