Working within our multidisciplinary teams on major product development projects, you will be responsible for supporting compliance at CDP within the ISO 13485, ISO 9001 and ISO 27001 Management System. The role also includes supporting a selection of clients on a range of products and processes in primarily the medical sector.
You will come from a Design and Development background and have a good understanding of New Product Development/Transfer to Manufacture. A fantastic time to join the team, you will have numerous projects to get stuck into and immediately add value. This role will suit an ambitious individual who is looking for career advancement and training and development opportunities. Positive, professional and confident you will have the ability to attend client meetings and lead projects in the future.
Your duties will include:
- Perform Internal Audits
- Hosting and SME at External Audits
- RCA facilitator for NC
- Owner NC/CAPA
- Monthly Metric Reporting
- Supplier Approval
- Support eQMS training for new starters
- Process owner within the Management System
Labs
- Support Production Manager to ensure compliance in the US labs
- Monthly Audits of the US labs
- Management of US assets in the eQMS
Training
- Presenting US QMS Induction
- Ensure US training events are recorded and stored appropriately
- Define project specific training plans
Project
- Quality Specialist for Client Projects including New Product Development, Transfer to Manufacture and Quality Projects e.g. DHF Remediation