Description
A global biopharmaceutical organisation is urgently looking for a Senior Cleaning Validation Engineer to support an ongoing compliance program.This is an exciting opportunity to work in dynamic, fast paced atmosphere, with lots of long term project opportunities coming up.
Location: Copenhagen area, Denmark
Duration: 6 months +
Start: ASAP
Role and Responsibilities:
• Co-ordinating cleaning validation activities on automated CIP systems within the downstream production area
• Preparing and executing cleaning validation protocols
• Writing validation summary reports
• Supporting the requalification of existing equipment (IQ/OQ)
• Implementing solutions to validation related deviations
Requirements:
• Degree educated in Scientific or Engineering discipline or equivalent experience
• Experience in co-ordinating, planning and executing cleaning validation protocols
• Knowledge of biopharmaceutical purification equipment (filtration, chromatography, tanks…)
• Able to independently coordinate and complete validation activities to a high standard
Apply now for further information.