Cache of job #13779158

Job Title

QA Engineer - Shift

Employer

Brightwater

Location

Waterford

Description

This is an exciting opportunity to join one of the most desirable employers in Waterford in a permanent role. Excellent salary and benefits package on offer for the right candidate. The Quality Engineer is instrumental in providing support to the Manufacturing Quality Manager to ensure that the manufacturing operation produces product that meets specifications within a manufacturing environment that complies with all relevant standards. This role is a shift position. You: 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 prioritize. Responsiblities: 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 PFMEAs , 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. Additional requirements of the job will be specified by the Manufacturing Quality Manager. For more on the role call Nigel on 021 4221000 or send your CV for consideration. This job originally appeared on RecruitIreland.com.

Date Added

2471 days ago

Apply