Office including Excel, Word, Outlook, PowerPoint, Docusign, Adobe and Adobe Editor an advantage. Knowledge and experience of regulatory systems and approvals including MDR and ISO13485 an advantage. Salary & Benefits £25,000 per annum You'll receive a fantastic benefits package including pension scheme, Private Medical, healthcare cover more »
co-ordination of projects with other departments. This job will aid in the maintenance of compliance to relevant cGMP, FDA QSR 21 CFR 820, ISO13485 & European Medical Devices Directive MDD94/42/EEC. Key Responsibilities Deputy to the QM Maintain and improve quality compliance. Identify, manage, and implement continuous … interactions internally and externally. Ability to provide solutions to difficult technical issues associated with specific projects. Experience in medical device industry/Knowledge of ISO13485 & FDA QSR requirements. Knowledge of world class quality techniques and implementation. Good working knowledge of validation, data integrity, statistics, technical drawing and tolerancing. Knowledge of more »
similar. Experience in process and product validation (sterile packaging according to ISO 11607 would be advantageous). Understanding of a quality management system (ISO13485/FDA) and medical device manufacturing advantageous. Very good MS-Office skills, especially Excel. Strong organizational skills with the ability to communicate at all levels more »
