Associate Quality Engineer

Job title:

Associate Quality Engineer

Company

Stryker

Job description

Work Flexibility: Onsite24/5 shift pattern23 month contractWhat you will do:Day to Day Activities:

  • ·Taking direction from Quality Engineer’s/Quality Team Leader as to how best to deploy resources and effort on the operations floor.
  • ·Provision of out-of-hours support to the business as required by management or as mandated by shutdowns and/or equipment failures.
  • ·Daily production line monitoring and the identification and quantification of process problems, along with subsequently implementing the necessary improvements and/or controls
  • ·Regular communication with the Manufacturing Team Members regarding issues, concerns and watch-outs on the lines.
  • Actively interfacing with cross-functional team members and suppliers, and always practicing good team work in support of the day to day operating requirements, and in pursuit of achieving the business targets

Inspection:

  • Assist in the develop and maintenance of sampling and inspection procedures
  • Sample, inspect and record inspection results when required
  • Control movement of components / products following inspection
  • Conduct MRB forums

Quality Improvements:

  • Provide effective and responsive QA support to Operations to resolve in-house, customer and supplier issues.
  • Support implementation of plant wide quality system improvements.
  • Work cross functionally with such groups as Regulatory, Product Development and Operations to ensure all issues are successfully resolved.
  • Support/ act as local subject expert for review, creation and training of divisional/corporate procedures.

Manufacturing Support:

  • Support Manufacturing Cell in addressing Quality Metrics, e.g. e.g. CAPA, Validations, NCR, Quality Awareness Tests, Training, ECR’s and Internal Audit Findings.
  • Responsible for input to Quality Metrics
  • Participate in the development and Continuous Improvement of the manufacturing processes for existing and new products. Coordination of PPAP activities.
  • Provide functional expertise to other support function on quality related issues.
  • Lead training activities on Quality related Procedures, e.g. Compliance, GMP, Audit Prep and GDP.
  • Coordination of MRB activities to the business unit to ensure the timely assessment of potential non-conforming products.
  • In conjunction with Team Lead approval, has the authority to order the cessation of production and product shipments in the event of a non-conformance arising. In conjunction with Team Lead approval, also has the authority to order the recommencement of production provided he/she is satisfied that all issues pertaining to the non-conformance have been addressed.
  • Support the creation & presentation the Monthly Business Unit review Slides and Represent Quality at this forum.
  • Represent Quality at the Weekly FPY (First Pass Yield) forum; Review the FPY Slides for trends and update as required from a Quality perspective

Customer Complaints:

  • Give input into the evaluation of Customer Complaints (PER Investigation) as required.
  • Problem solving / Trouble shooting of customer complaint investigations, coordination of root cause and risk assessments associated NC’s and Risk Assessments where required.

NCR/CAPA:

  • Support the NCR/CAPA Process.
  • Participate in risk assessment activities and ensure that all failure modes in process have been identified and addressed.
  • Participate in Problem Solving meetings using the following: 4D, Six Sigma, etc.
  • Ensure that Containment of product is properly addressed and Documented
  • Ensure that Corrective Actions clearly actioned and documented.

Validation:

  • Assist in completion of equipment validation ((VP, IQ, OQ, PQ, MSA, IPF’s, PSP’s, FR’s etc.).
  • QA review and approval of unplanned Pemac routines.

Auditing:

  • Participate in Internal Audits as required and Supplier Audits. if required.
  • Support site during External Audits. (i.e. FDA, IMB and BSI).

Risk:

  • Understand and ensure compliance to ISO 14971 ‘Risk management’.
  • Ensure that the Top Down Risk Documents, Bottom Up Risk Documents and Attribute Charts are current and live.

What you will need:Must have completed Degree or be working towards completion of Degree in Engineering, Science or equivalent (NFQ level 7)· Minimum 1-2 years experience in a regulated industry· Preferably 1-2 years experience in a QA roleTravel Percentage: 0%

Expected salary

Location

Cork

Job date

Sat, 22 Jun 2024 01:51:04 GMT

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