Front End QA Inspector 3: Cleanroom Lot Release

Dexcom Inc.

Athenry

Vor Ort

EUR 35.000 - 46.000

Vollzeit

Vor 8 Tagen
Bewerbungsgenerator

Eine vollständige Bewerbung in einer Minute — maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Comprehensive benefits
Global growth opportunities
Career development

Zusammenfassung

Dexcom Inc. in Athenry, Ireland is seeking a QA Inspector 3 for our first European manufacturing site.

This on-site role operates on a fixed day shift (7am–7pm) Mon-Wed with alternate Thursdays, part of a 4-on/3-off and 3-on/4-off cycle, in a cleanroom environment focused on Lot Release responsibilities. You will review in-process and final documents, perform inspections, maintain GDP-compliant records, and collaborate with Quality Engineers and Manufacturing to ensure products meet GMP

Qualifikationen

  • Minimum Level 6 in Quality, Engineering or a related discipline.
  • 4–6 years’ experience within the medical device industry.
  • Strong interpersonal and teamwork skills with written and verbal communication.
  • Ability to flex to work in different shifts to meet demand.

Aufgaben

  • Performs in-process and final product review of documents for GDP and proper dating and sign-offs.
  • Performs in-process product inspection and testing per product specs and QA standards.
  • Manage Lot Release transactions in the defined system and maintain inspection reports.

Kenntnisse

Interpersonal skills
Teamwork
Communication (written and verbal)
Flexibility with shifts

Ausbildung

Level 6 in Quality/Engineering or related discipline

Tools

Minitab
Microsoft Office Suite

Jobbeschreibung

Dexcom Inc. in Athenry, Ireland is seeking a QA Inspector 3 for our first European manufacturing site.

This on-site role operates on a fixed day shift (7am–7pm) Mon-Wed with alternate Thursdays, part of a 4-on/3-off and 3-on/4-off cycle, in a cleanroom environment focused on Lot Release responsibilities. You will review in-process and final documents, perform inspections, maintain GDP-compliant records, and collaborate with Quality Engineers and Manufacturing to ensure products meet GMP

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