QA Inspector 3 (Front End 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

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.

Meet the team:

Product Testing and Lot Release Department within our Quality Assurance team are looking for a dynamic and skilled Lot Release QA Inspector 3 (Onsite role) to support the start-up of our first European manufacturing site in Athenry. As a member of the Lot Release team, the inspector plays a critical role in ensuring that the products meet all regulatory, quality, and safety standards before being released for commercial use. The inspector is responsible for ensuring the activities related to product Lot Release are performed in a manner which meets company standards and methods as determined by the Quality Assurance or other Engineering departments.

Where you come in:

• You will perform 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.
• You will 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.
• You will 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.
• You will ensure all documentation and labelling is legible, complete, and correct per current Good Manufacturing Practices
• You will assist in setting up the Lot Release Dept. and associated Lot Release Lab.
• You will assist in carrying out TMVs and troubleshooting test methods
• You will initiate and assist with the NCMR process during manufacturing of commercial products.
• You will adhere 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 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

Education and Experience Requirements:

• You have a minimum Level 6 in Quality, Engineering or a related discipline.
• You have 4 -6 years’ experience within the medical device industry.

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%

Dexcom Warriors | Meet Dexcom heroes and read their stories | Dexcom Reviews | Dexcom

Read success stories from people who rely on Dexcom CGM devices every day. At Dexcom, our customers are our heroes - read our Warrior stories to learn more.

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 €35,445.00 to €45,870.00 gross. Final offer will depend on your qualifications, competencies, and professional experience.