Job description
To ensure compliance with cGMP, ISO13485 and regulatory requirements, through quality management (QMS) in the QA department: Assisting to clear a backlog of SAP tasks related to incidents, changes, customer complaints and document reviews. Ensure that risk assessments are completed, filed and reported on when required. Complete all the open notifications and document reviews as assigned within the agreed timelines. 2 years' experience in a Pharmaceutical Manufacturing or Quality Assurance divis…