Description
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.