Tech, Operations

Newyorkbioconnect

Salamanca, Spain
Gmp compliance
Quality standards
Sap transactions
The IPT Producción de Estériles is responsible for the manufacturing and packaging of sterile pharmaceutical products following 'Safe by Choice – Quality Always' principles

Job Summary

  • The IPT Producción de Estériles is responsible for the manufacturing and packaging of sterile pharmaceutical products following 'Safe by Choice – Quality Always' principles.
  • The role involves performing FPU packaging tasks, including quality checks, material reception, workspace preparation, and environmental monitoring.
  • This position requires adherence to GMP regulations, local procedures, and participation in process improvement and deviation investigations.

Matching Summary

The IPT Producción de Estériles is responsible for the manufacturing and packaging of sterile pharmaceutical products following 'Safe by Choice – Quality Always' principles.

Skills & Requirements

Must-have

  • GMP compliance
  • Quality standards
  • SAP transactions
  • Cleanroom procedures
  • Material handling

Nice-to-have

  • Organized and team-oriented
  • Continuous improvement participation
  • Risk identification and communication

Key Requirements

  • Professional training
  • 1 year of experience in pharmaceutical production/laboratory
  • Knowledge of GMP and quality systems
  • Basic English proficiency
  • Shift work availability

Work Rights

Not specified

Tailored Resume

Cover Letter