Process Engineer

Katalyst Healthcares & Life Sciences

Durham, NC

JOB DETAILS
SKILLS
Asepsis, Automation, Biomedical Engineering, Chemical Engineering, Commissioning, Communication Skills, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Current Good Manufacturing Practice (cGMP), Drug Manufacturing, Equipment Validation, FDA Requirements, GMP (Good Manufacturing Practices), Identify Issues, Industrial Engineering, Manufacturing, Manufacturing Engineering, Manufacturing Operations, Mechanical Engineering, Operational Support, Process Engineering, Process Improvement, Process Manufacturing, Process Validation, Project Engineering, Quality Assurance, Regulations, Root Cause Analysis, Startup, System Start-Up, Technical Consulting, Technical Writing, Writing Skills
LOCATION
Durham, NC
POSTED
1 day ago
Responsibilities:
  • Seeking an experienced Process Engineer – Cartridge Filling to support a large-scale sterile pharmaceutical manufacturing expansion. This consultant will provide technical expertise for cartridge filling operations, supporting equipment implementation, startup, commissioning, qualification, process optimization, and commercial manufacturing.
  • Working closely with Manufacturing, Quality Assurance, Validation, Automation, Maintenance, and Project Engineering, this individual will ensure cartridge filling processes consistently meet production, quality, and regulatory objectives while supporting the successful startup of new manufacturing operations.
  • Direct experience supporting cartridge filling lines is required. Candidates with experience limited to syringe filling will not be considered.

Requirements:

  • Bachelor's degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Manufacturing Engineering, Industrial Engineering, or a related engineering discipline.
  • 5+ years of pharmaceutical manufacturing experience, preferably supporting sterile injectable operations.
  • Hands-on cartridge filling experience is required.
  • Strong understanding of FDA cGMP regulations, EU GMP, Annex 1, and aseptic manufacturing principles.
  • Experience supporting equipment validation, process qualification, and manufacturing startup activities.
  • Excellent troubleshooting, communication, and technical writing skills.

Most Important Skills Needed:

  • Direct cartridge filling line experience (Required)
  • Process Engineering within sterile pharmaceutical manufacturing
  • Aseptic filling operations
  • Equipment startup, commissioning, and qualification (FAT, SAT, IQ, OQ, PQ)
  • Process optimization and manufacturing troubleshooting
  • GMP manufacturing experience
  • Root cause investigations, CAPA, and deviation support
  • Cross-functional collaboration with Manufacturing, Validation, Automation, and Quality
  • Technical documentation, engineering studies, and protocol development

About the Company

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Katalyst Healthcares & Life Sciences