Shift Quality Engineer
Shift Quality Engineer - County Waterford. Principal Responsibilities of this position: • Liaise with shift management to manage the Manufacturing operation to provide the required volume output per shift which complies with all quality and regulatory requirements. • Determine appropriate lot disposition decisions on a shift by shift basis. • Manage, review & approve any non-conformances that may occur. • Provide quality oversight for manufacturing, including approval of validation documentation, updating PFMEA's, manage CAPA activity & continuous improvement. • Act as the MQM interface with Operations and engineering functions. • Disposition product as appropriate & manage any non-conformance activity. • Highlight relevant issues and participate / lead resolution. • Understand and review Validation documentation, Change Requests, Design and Process FMEA’s. • Participate in Quality System Continuous Improvement activities. • Ensure regulatory compliance to GMP’s of applicable medical device regulatory agencies (eg, FDA, ISO and MDD) and internal documentation. • Provide direction to ensure product quality is maintained at all stages of the manufacturing operation. Interested applicants should have: • Minimum 3 years’ experience in a regulated pharmaceutical/medical device environment. • Manufacturing quality experience desirable. • Full understanding of the requirements of the Regulatory Standards. • Experience in Quality auditing an advantage. • Experience in using Microsoft Office products. • Experience of working in a team environment. • Third level Qualification in Science or Engineering. • Statistics/Six Sigma qualification an advantage. • Good communication skills. • The ability to motivate and influence people. • Self-starter, highly motivated with the ability to prioritise. • High attention to detail. This job originally appeared on RecruitIreland.com.
9 days ago