Description
A Biotechnology company near Copenhagen in Denmark is looking for a Cleaning Validation Engineer to aid the current team with the huge workload. This individual ideally would start ASAP. There are multiple projects to get involved with after the intial contract, as such this is a very exciting project to be involved in. The site has £120 million new project, and many refurbishment projects (approx. £20 million each).Responsibilities:
• Preparing and executing cleaning validation protocols on production equipment
• 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
• 5-10 years’ in validation including experience planning and executing cleaning validation activities
• Bio/Pharmaceutical manufacturing environment
• Knowledge of automated CIP systems
• Able to independently carry out validation activities with minimal support or guidance
• Ideally Autoclave experience (KAYE validator)