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.

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

Shift Premium: 15% premium only for Sat/Sun, no shift premium for Thurs/Fri

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 2 (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

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

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.
You have proficiency with statistical analysis (e.g. Minitab) and Microsoft Office Products (Word, Excel, Outlook ) is desirable

Experience and Education Required:

You have a minimum Level 6 in Quality, Engineering or a related discipline.
You have 2-4 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.

To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.

#DexcomIreland

QA Inspector 2 (Back End Day Shift)

Benefits

Job Description