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Shift Quality Lead

Location: Dublin South, Dublin
Salary: Negotiable
Posted: about 2 months ago
Role type: Permanent
Industry: Science, Technology and Operations Practice (STO)
Contact name: Maeve Fahey
Contact email: maeve.fahey@hrmrecruit.com

Job description

Our client, a global medical device and diagnostic organisation, are seeking an experienced Shift Quality Lead to join the team at their state-of-the-art manufacturing facility in South Dublin.

The Shift Quality Lead will be responsible for active participation in non-conformance investigations and lot disposition decisions, raising of Quality notifications in response to quality non-conformances and ensuring corrections are completed and confirmed on assembly processes.

The Role

Duties and responsibilities of the Shift Quality Lead will include:

  • Monitoring the activities of the Quality Control Lab to ensure optimal efficiency and compliance with all regulatory requirements in the QC lab environment.
  • Preparation of relevant work sheets and execution of In Process inspection tests.
  • Ensure required quality testing is carried out; carry out inspections to meet the standard set by the organization Participate in the Change Control Process.
  • Review In process controls, SOP's, Test Methods, and specifications to ensure Lab inspections are being carried out as per design intent.
  • Analysis of data, quality metrics and trends of in-process inspection data.
  • Liaise with relevant personnel regarding flow of product through QC department and other issues that arise.
  • Preparation, review and approval of technical documentation and perform training as required in the area.
  • The Shift Quality Lead will provide QA support to the shift manager when required.

The Person

You will have skills and experience in the following:

  • Bachelors degree in Science or similar
  • Degree incorporating some elements of Quality Assurance preferred
  • 3+ years of experience in a similar position in a fast-paced, high volume manufacturing facility
  • Good knowledge of ISO standards and FDA
  • Experience using SAP and Trackwise

To discover more about this opportunity, apply now or contact Maeve Fahey at HRM on +353 1 632 1885 for a confidential discussion.

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Maeve Fahey

Science Recruitment Consultant

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