Why join Stryker?
Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development.
We are proud to be named one the Named a Best Workplace in Europe by Great Place to Work for the fifth consecutive year! AND Best Workplace for Diversity by Fortune Magazine! Learn more about our award-winning organization by visiting stryker.com
Inspector, Quality - 12 Month Contract (Strong possibility of permanent role on completion of the contract)
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Shift: Night Shift - Monday - Thursday 8.00 pm - 6.30 am.
Location: Belfast
Hourly Rate: £11.62 + 33% Shift Premium (£15.49 Hourly Rate)
Performs inspection of manufacturing goods & documentation during the manufacturing process. Conduct visual, dimensional and electrical inspection of sub-assemblies or final systems assemblies. Interprets prints, manufacturing drawings, diagrams, wire cards and lists in approving or rejecting in-process or final assemblies.
Under general supervision, the Quality Inspector will perform inspection and testing activities of product in the incoming receipt, manufacture, packaging and /or release of Medical Devices at Stryker, ensuring product quality and throughput goals are met. Ensure compliance to procedures and practices at all times.
What you will do:
Working within the Inspection Team, is responsible for inspection related activities, specific to the sites' requirements, may include but not limited to the following:
- Perform dimensional and/or visual inspection to blueprint using gauges and other reliant inspection equipment.
- Perform material and component inspections.
- Perform First Article Inspection (FAI) and verify FAI data (incl. statistical analysis) is acceptable.
- Read and inspect to blueprints and/or inspection guide sheets / instructions.
- Perform Document Review, analyse, inspect and archive DHRs (paper-based and/or electronically) in compliance to GMP/GDP requirements prior to release to finished goods.
- Perform computer system transactions related to router inspections, etc.
- Segregate, quarantine and complete documentation for non-conforming materials when necessary.
- Initiation of quarantine tickets (non-conformance reports)
- Perform product release disposition tasks in the ERP system
- Support the achievement of Inspection Teams' KPI's.
- Work to forecasts and plans based on Business requirements.
What you will need:
- 1+ year's relevant experience in GMP manufacturing environment
- Strong verbal, written and interpersonal skills.
- Proven self-motivated and able to prioritize and resolve competing priorities.
- Previous experience working in an electronics environment beneficial