You will be working for a leading global manufacturing group that have operations across both pharmaceuticals and chemical manufacturing. They have sites globally with a number of those sitting within the US. The US arm of the business is going through an exciting growth period.
They are looking at revolutionizing the Quality division which is currently very manual and paper based. Your role would be to make a decision on a digital Quality Management System and implement this, supporting the wider team with this transition.
Responsibilities
- Select the most suited Quality Management System for the business, working with the wider leadership team
- Design and implement the agreed Quality Management System
- Developing the Quality systems for the business including CAPA audits & supplier quality
- Perform internal and external quality audits and compile detailed reports of findings
- Support the wider Quality team with coaching and leading through this transition
Qualifications
- 5+ years' relevant work experience
- Implementation of a Quality Management System previously
- Team management experience
