Validation & Engineering Officer

Experience supporting qualification and validation activities for facilities, utilities, equipment, processes or computerised systems. Experience authoring and executing validation and qualification documentation. Knowledge of EU GMP requirements and qualification lifecycle activities including DQ, FAT, SAT, IQ, OQ and PQ.

Strong analytical, problem-solving and investigation skills The ability to manage multiple priorities while maintaining a high level of attention to detail. Excellent communication skills and a collaborative approach to working with stakeholders across the business. It would be great if you also have Experience within aseptic manufacturing or pharmaceutical compounding environments.

Knowledge of cleanroom qualification, HVAC systems, critical utilities or environmental monitoring systems. Exposure to isolator technology, VHP decontamination systems or Computerised Systems Validation (CSV). An HNC, HND, degree or equivalent qualification in Engineering, Pharmaceutical Sciences, Biotechnology, Life Sciences or a related discipline