Onsite QA Inspector - Lot Release (12h Day Shift)

Dexcom Inc.; Athenry; On-site; EUR 35,000 - 46,000; Full time

Benefits offered by this job

Comprehensive benefits program

Career development

Tuition reimbursement

Global growth opportunities

Job summary

Dexcom Inc. is seeking a Lot Release QA Inspector 3 for our new European manufacturing site in Athenry, Ireland. This onsite role involves performing in-process and final product reviews and ensuring GDP compliance for release of commercial products.

You will collaborate with Quality Engineers, Manufacturing, and Process Engineers to resolve issues, maintain GMP documentation, and support setup of the Lot Release Lab. Requires Level 6 in Quality/Engineering and 4–6 years in medical devices.

Qualifications

• Minimum Level 6 in Quality, Engineering or related discipline.
• 4–6 years of experience in the medical device industry.

Responsibilities

• Review in-process and final release documents for GDP standards.
• Inspect and test in-process and final products per specifications.
• Enter and manage Lot Release transactions in the system.
• Collaborate with Quality, Manufacturing and Process Engineers on issues.
• Maintain SOP compliance and ensure staff training.
• Monitor equipment, ensure cleanliness and safe operation.
• Prepare documentation and labeling accuracy per GMP.
• Assist setup of Lot Release Lab and TMVs.
• Lead or assist NCMR activities during manufacturing.
• Adhere to GMP and safety guidelines.

Skills

Interpersonal skills

Written and verbal communication

Teamwork

Flexibility

Statistical analysis (Minitab)

Education

Level 6 in Quality/Engineering

Tools

Minitab

Microsoft Office

Job description

Dexcom Inc. is seeking a Lot Release QA Inspector 3 for our new European manufacturing site in Athenry, Ireland. This onsite role involves performing in-process and final product reviews and ensuring GDP compliance for release of commercial products.

You will collaborate with Quality Engineers, Manufacturing, and Process Engineers to resolve issues, maintain GMP documentation, and support setup of the Lot Release Lab. Requires Level 6 in Quality/Engineering and 4–6 years in medical devices.