Process Engineer

Karwell Technologies
  • Frederick, MD
  • Quick Apply
15 days ago

Job Description

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

Numbers & Facts

LocationFrederick, MD

Skills

  • Asepsisunmatched
  • Automationunmatched
  • Biomedical Engineeringunmatched
  • Chemical Engineeringunmatched
  • Commissioningunmatched
  • Communication Skillsunmatched
  • Corrective and Preventative Action (CAPA) Systemsunmatched
  • Cross-Functionalunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Drug Manufacturingunmatched
  • Equipment Validationunmatched
  • FDA Requirementsunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Identify Issuesunmatched
  • Industrial Engineeringunmatched
  • Manufacturingunmatched
  • Manufacturing Engineeringunmatched
  • Manufacturing Operationsunmatched
  • Mechanical Engineeringunmatched
  • Operational Supportunmatched
  • Process Engineeringunmatched
  • Process Improvementunmatched
  • Process Manufacturingunmatched
  • Process Validationunmatched
  • Project Engineeringunmatched
  • Quality Assuranceunmatched
  • Regulationsunmatched
  • Root Cause Analysisunmatched
  • Startupunmatched
  • System Start-Upunmatched
  • Technical Consultingunmatched
  • Technical Writingunmatched
  • Writing Skillsunmatched

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