Transforming Lives through Quality and Innovation
As a Quality Inspector at Edwards Lifesciences, you will play a vital role in creating medical devices that make a meaningful difference to patients worldwide.
Our Manufacturing teams design and develop innovative technologies, tools, and devices that transform patients' lives. Your attention to detail and commitment to continuous improvement will help us turn these ideas into reality, leaving a lasting and positive impact on patient lives.
Key Responsibilities:
1. Assessment and Inspection:
o Perform visual, dimensional, and functional inspection of various components and finished medical device products using specialized tools and equipment, including magnifying lamps, microscopes, and vision inspection systems.
o Ensure conformance with design specifications while working independently with a high level of productivity.
1. Audit and Compliance:
o Conduct operational audits and documentation reviews to ensure compliance with applicable procedures and documentation standards.
o Review, follow, and perform job functions in compliance with established work instructions and adherence to SOPs.
1. Documentation and Communication:
o Record traceable information on device history records and utilize computer programs to perform and/or document specific job tasks.
o Provide core team feedback, including escalating work issues and changes in the final devices and raw materials to higher levels (e.g., Engineering Support) for assessment and correction.
Requirements:
* Minimum 2 years of previous related experience, including GMP and GDP.
* Leaving Certificate or equivalent.
* Good communication skills.
* Basic computer skills, required, including working knowledge of manufacturing software.
* Full understanding of applicable inspection procedures.