Quality Inspector - Evening Shift

Role overview

Join a quality-focused manufacturing environment where your attention to detail helps support devices that can improve patient outcomes worldwide. In this role, you will inspect in-process and completed products, check supporting records, and carry out audits to confirm that all items meet company procedures, regulatory requirements, and defined operating standards.

Working schedule

This position follows a four-day week: Monday to Wednesday from 4:30 PM to 3:00 AM, and Thursday from 4:30 PM to 2:00 AM.

Key responsibilities

• Carry out visual, dimensional, and functional inspections on a broad range of components and finished medical device products using tools such as magnifying lamps, microscopes, vision inspection systems, and related equipment.
• Use a microscope for inspection activities in line with the applicable standard operating procedures, and operate automated inspection equipment where required to confirm dimensional specifications.
• Test more complex finished medical devices using both automated and manual valve testing equipment to confirm design compliance.
• Perform operational audits and review documentation to verify adherence to procedures and documentation standards.
• Follow established work instructions and SOPs, including accurate recording of traceability data in device history records and use of computer systems to complete and document tasks.
• Escalate issues, defects, and changes in final devices or raw materials to appropriate support teams such as Engineering for review and correction.
• Complete line clearance activities and verify inspection status.
• Check manufacturing documentation against component and device drawings.
• Help train other inspectors by demonstrating tasks and providing feedback.
• Contribute to smooth shift handovers by briefing the next shift on work status when needed.
• Take part in special assignments such as test method validations, protocol work, first article inspection, and similar activities.
• Arrive on time, maintain regular attendance, and be available for full work periods of eight hours or more.
• Handle general housekeeping duties in the work area.

Experience and education

The role requires 2 years of relevant prior experience, with GMP and GDP experience required. A Leaving Certificate or an equivalent qualification is preferred.

Additional skills and working requirements

You should be able to communicate clearly, read and write English confidently, and work with basic computer systems, including manufacturing software. Strong accuracy, steady hand-eye coordination, and high manual dexterity are important, along with a solid understanding of inspection procedures and the ability to improve your inspection skills over time. You will also need to clearly explain nonconformance issues and enter them into the quality management system. The role calls for teamwork, limited supervision, the ability to follow detailed instructions, and the willingness to give and receive feedback. You must also comply with environmental, health, safety, cleanroom, pandemic, and other company rules, while taking the required steps to protect people and the environment from harm and pollution.

About the quality team

The quality function plays a critical role in supporting the development of advanced technologies by ensuring every stage of the process meets high standards for integrity and safety. The team works closely with different functions to support decisions across the full product lifecycle.