QC Inspector II — Evening Shift, Medical Devices

36 Dexcom International Limited; Athenry; On-site; EUR 32,000 - 42,000; Full time

Benefits offered by this job

Full benefits

Global growth opportunities

Career development programs

Tuition reimbursement

Job summary

Dexcom Ireland is seeking a QC Inspector 2 for our first European manufacturing site in Athenry. The role focuses on inspecting components, materials, sub-assemblies and products to ensure conformity with specifications and QA standards. You will prepare inspection reports and work with QA engineers to resolve issues.

Role requires 2–4 years in medical devices, Level 6 in Quality/Engineering, and ability to cover shifts. Onsite role with a strong benefits package and career growth opportunities.

Qualifications

• Minimum Level 6 in Quality, Engineering or a related discipline.
• 2–4 years' experience within the medical device industry.
• Strong interpersonal and teamwork skills.

Responsibilities

• Perform inspections, check testing and sampling procedures for incoming components, materials, sub-assemblies and products to ensure conformance to requirements.
• Prepare, record, and update receiving inspection report forms with accurate information.
• Perform transactions related to RI Materials in a defined system.
• Work closely with Quality Engineers, Supplier Quality Engineers and other functions on material, equipment or test issues.
• Monitor equipment and instrumentation to ensure safe operation.
• Adhere to GMP, safety guidelines and company standards.
• Participate in setup of the Receiving Inspection Dept. and RI Lab.
• Perform other duties as assigned.

Skills

Interpersonal skills

Teamwork

Written & verbal communication

Flexibility

Education

Level 6 in Quality or Engineering

Tools

Smartscope

Keyence

Job description

Dexcom Ireland is seeking a QC Inspector 2 for our first European manufacturing site in Athenry. The role focuses on inspecting components, materials, sub-assemblies and products to ensure conformity with specifications and QA standards. You will prepare inspection reports and work with QA engineers to resolve issues.

Role requires 2–4 years in medical devices, Level 6 in Quality/Engineering, and ability to cover shifts. Onsite role with a strong benefits package and career growth opportunities.