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Cleaning Validation Engineer

Eingestellt von Quanta Consultancy Services

Gesuchte Skills: Support, Engineering, Engineer

Projektbeschreibung

A global biopharmaceutical company is looking for a Cleaning Validation Engineer to support its manufacturing operations in Denmark.

Location: Copenhagen area, Denmark

Duration: 3-6 months

Role and Responsibilities:
Preparing and executing cleaning validation protocols
Carrying out cleaning validation tests on production equipment and CIP systems
Reviewing cleaning validation test results and writing summary reports
Supporting autoclave validation activities and thermal mapping using KAYE validator
Ensuring that all validation activities are carried out in compliance with corporate and GMP standards

Requirements:
Degree educated in Engineering or Scientific discipline or equivalent experience
Experience planning and executing cleaning validation activities within a (bio) pharmaceutical manufacturing environment
Knowledge of automated CIP systems
Able to independently carry out validation activities with minimal support or guidance

Apply now for the opportunity to work in Europe's busiest biopharmaceutical cluster.

Projektdetails

  • Einsatzort:

    København, Dänemark

  • Projektbeginn:

    asap

  • Projektdauer:

    3 - 6 months

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Quanta Consultancy Services