QC Inspector II - Evening Shift, Receiving & Lab Setup

Dexcom; Ireland; On-site; EUR 32,000 - 42,000; Full time

Benefits offered by this job

Benefits program

Growth opportunities

Tuition reimbursement

Career development

Job summary

Dexcom Ireland is hiring for a Receiving Inspection QC Inspector 2 position to support the startup of our first European manufacturing site in Athenry. You will inspect incoming components, prepare RI reports, and work with Quality Engineers to resolve issues.

The role is onsite with GMP and safety compliance expected. The successful candidate has 2–4 years in medical devices, strong teamwork, and proficiency with inspection tools like Smartscope and Keyence, with a shift pattern to cover

Qualifications

• Minimum Level 6 in Quality, Engineering or related discipline.
• 2–4 years’ experience in the medical device industry.
• Experience with inspection equipment (Smartscope, Keyence) preferred.

Responsibilities

• Perform inspections, check testing and sampling for incoming components and products to ensure conformance to requirements.
• Prepare and update receiving inspection report forms and ensure paperwork is accurate.
• Record RI transactions in the defined system.
• Collaborate with Quality Engineers and other functions on issues related to materials or tests.
• Monitor equipment and instrumentation to ensure safe operation.
• Adhere to GMP, safety guidelines and company standards at all times.
• Assist in setup of the Receiving Inspection Dept. and RI Lab.
• Perform other duties as assigned.

Skills

Interpersonal skills

Teamwork

Written & verbal communication

Education

Level 6 in quality/engineering

Quality/Engineering diploma

Tools

Smartscope

Keyence

Minitab

Job description

Dexcom Ireland is hiring for a Receiving Inspection QC Inspector 2 position to support the startup of our first European manufacturing site in Athenry. You will inspect incoming components, prepare RI reports, and work with Quality Engineers to resolve issues.

The role is onsite with GMP and safety compliance expected. The successful candidate has 2–4 years in medical devices, strong teamwork, and proficiency with inspection tools like Smartscope and Keyence, with a shift pattern to cover