Strong technical background in a complex manufacturing environment
Ability to understand and interpret Statistical Process Control and Capability
Understanding of LEAN principles & practitioner of Problem-Solving skills
Analytical skills to develop solutions/make judgements within general operating guidelines
Project Management skills, innovative in challenging ways of working and proposing alternative methods of working
High levels of concern for standards, attention to detail with a self-motivating and proactive approach, including understanding and application of cGMP
Requirements
Experience of preparing and managing qualification, experimental and validation protocols of work
Sound working knowledge and understanding of pharmaceutical manufacturing processes
Six Sigma Green belt qualification
Degree in Science or Engineering
Validation process ownership and delivery
Experience of working within an aseptic environment and managing the challenges this brings