Manufacturing Technician

  • by
Location
Candidate No.
1963368

About this Candidate

DAVRON CV: Candidate 1963368

MANUFACTURING TECHNICIAN | ASEPTIC & MEDICAL DEVICE PRODUCTION | MECHANICAL ASSEMBLY & GMP COMPLIANCE

Core Expertise

  • Aseptic manufacturing and cleanroom operations for cell therapy and sterile medical products.
  • Mechanical and electrical assembly of complex subassemblies using engineering drawings and precision hand tools.
  • cGMP and ISO-compliant documentation management including batch records, SOP adherence, deviations, and CAPA.
  • Troubleshooting and production support to reduce downtime and sustain manufacturing throughput.
  • Prototype assembly and engineering support for thermal and gas-purification systems.

Project Background

  • Assembled gas purification and preheater systems using piping, valves, sensors, and electrical wiring.
  • Produced autologous cell therapy products through sterile processing, harvesting, freezing, and controlled-rate freezing.
  • Manufactured single-use polymer medical bags and performed polymer sealing and label/batch record control.
  • Supported thermal engineering prototypes and test setups for aerospace and health-sector projects.
  • Implemented systematic line-clearance and decontamination verification to reduce contamination risks during changeovers.

Key Skills

  • AutoCAD | SolidWorks
  • Aseptic manufacturing | Cleanroom operations
  • cGMP | ISO | SOP compliance | CAPA
  • Mechanical assembly | Electrical assembly | Prototype assembly
  • Batch records | Quality documentation
  • Troubleshooting | Production support | Equipment maintenance
  • Made2Manage | Microsoft Office

Education

  • B.S., Mechanical Engineering — California State University, Long Beach

Why Interview this Candidate?

They bring 9+ years in regulated pharmaceutical, medical device, and biopharma manufacturing with hands-on assembly, aseptic processing, and quality documentation experience. Proven to improve contamination control through a redesigned line-clearance verification procedure while supporting CAPA and deviation investigations. Ready to step into a lead manufacturing role to mentor operators and drive consistent, compliant production.

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