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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
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