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 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
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%
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Should a reasonable accommodation be necessary to aid a disability, requests should be sent to Dexcom Talent Acquisition at talentacquisition@dexcom.com.
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.
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