QA Inspector 2

Dexcom, Inc.; Athenry; On-site; EUR 32,000 - 42,000; Full time

Benefits offered by this job

Comprehensive benefits program

Growth opportunities

Career development programs

Global exposure to CGM tech

Job summary

Dexcom is seeking a QA professional for a fixed day shift pattern (12 hours, 7am–7pm, Mon-Wed and alternate Thu) in a cleanroom environment. You will review documents for GDP, inspect products, manage Lot Release, and collaborate with Quality, Manufacturing and Process Engineering to resolve issues while ensuring GMP compliance.

You will monitor equipment, maintain accurate labeling, and participate in setting up the Lot Release Lab.

Qualifications

• Minimum Level 6 in Quality, Engineering or related discipline.
• 2-4 years of experience in the medical device industry.
• Strong interpersonal and teamwork skills, plus written and verbal communication.
• Flexibility to work in different shifts to meet demand.
• Proficiency with statistical analysis (e.g. Minitab) and Microsoft Office.

Responsibilities

• Perform in-process and final product review of documents for GDP compliance.
• Conduct in-process product inspection and testing per specifications.
• Handle Lot Release transactions in defined systems.
• Collaborate with Quality Engineers, Manufacturing and Process Engineers on Lot Release issues.
• Maintain compliance with SOPs and complete required training.
• Monitor equipment and ensure clean, safe operation and labeling accuracy.
• Assist in setting up Lot Release Dept. and Lab, and in TMVs/testing methods.
• Support NCMR processes during manufacturing and ensure GMP adherence.

Skills

Quality assurance

GMP knowledge

Interpersonal skills

Communication skills

Analytical thinking

Shift flexibility

Minitab

Microsoft Office

Education

Level 6 in Quality, Engineering or related discipline

Tools

Minitab

Excel

Word

Outlook

Job description

The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.

We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.

Job Description

This role is on a fixed (non rotational) day shift pattern which will be a 12-hour shift (7am – 7pm) every Monday to Wednesday and alternate Thursdays, following a repeating 4-on/3-off – 3-on/4-off schedule.

This position is primarily cleanroom‑based and involves working in a controlled environment in line with established cleanroom procedures and quality standards.

Where you come in:

• Performs in-process and final product review of documents for accurate format, signatures, dating and Good Documentation Practices (GDP) for commercial product in a timely matter.
• Perform in-process product inspection and testing for commercial products as conforming to specified requirements in accordance with product specification and quality assurance standards. Prepares, records, and updates inspection report form.
• You will perform transactions related to Lot Release in a defined system.
• You will work closely with Quality Engineers, Manufacturing, Process Engineers and other functions on any issues that arise in relation to the Lot Release process.
• Maintain compliance with operating procedures and ensure training is completed prior to the operation of a task.
• You will monitor equipment and instrumentation to ensure there are no issues and equipment is clean, and safe to use.
• Ensure all documentation and labelling is legible, complete, and correct per current Good Manufacturing Practices.
• Assist in setting up the Lot Release Dept. and associated Lot Release Lab.
• You will assist in carrying out TMVs and troubleshooting test methods.
• Initiate and assist with the NCMR process during manufacturing of commercial products.
• Adheres to all GMP, safety guidelines and company standards at all times.
• You will assume and perform other duties as assigned.

What makes you successful:

• You will have a minimum Level 6 in Quality, Engineering or a related discipline.
• You will have 2-4 years’ experience within the medical device industry.
• You can demonstrate strong interpersonal and teamwork skills and written and verbal communication skills.
• You must be able to flex to work in different shifts to meet demand.
• Proficiency with statistical analysis (e.g. Minitab) and Microsoft Office Products (Word, Excel, Outlook) is desirable.

What you’ll get:

• A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
• A full and comprehensive benefits program.
• Growth opportunities on a global scale.
• Access to career development through in-house learning programs and/or qualified tuition reimbursement.
• An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.

Travel Required:

• 0-5%

AI in Hiring Notice

We may use AI supported tools to help make our hiring process more efficient, consistent, and accessible for candidates around the world. All hiring decisions are made by people.

At Dexcom, we are committed to providing a fair and inclusive recruitment process, and welcome candidates of all genders and gender identities to apply. If any wording in this description appears unintentionally gendered or exclusionary, please be assured this is not intentional.

Should a reasonable accommodation be necessary to aid a disability, requests should be sent to Dexcom Talent Acquisition at [e-mail].

The annualised base salary for this position is from €32,130.00 to €41,580.00 gross. Final offer will depend on your qualifications, competencies, and professional experience.