QA Inspector 3 - Evening Shift
Athenry, County Galway, Ireland · Full Time
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- Experience
- 4–6 yrs
- Salary
- EUR 35,445 – EUR 45,870 / year
- Openings
- 1
- Posted
- 5 hours ago
- Work mode
- In office
- Education
- Level 6 qualification in Quality, Engineering or related discipline
- Resume
- Required to apply
Where you'll work
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Job description
About the Company
Dexcom Corporation, a NASDAQ-listed leader in continuous glucose monitoring technology, has transformed diabetes management over the past 25 years and continues to innovate health solutions globally. The company is expanding beyond diabetes, aiming to develop personalized and actionable health insights for broader wellness challenges while maintaining high standards of biosensing technology.
Role Overview
This role involves a fixed evening shift schedule: Monday to Thursday from 3:30 PM to midnight (8-hour shifts), and Friday from 3:30 PM to 11:00 PM (7-hour shift) with a 20% shift premium. The position is primarily based in the laboratory, requiring adherence to controlled processes and quality benchmarks.
Responsibilities
- Review in-process and final product documentation for correct format, signatures, dating, and compliance with Good Documentation Practices (GDP) in a timely manner.
- Conduct inspections and testing on in-process and final commercial products to ensure adherence to specifications and quality standards. Prepare and update inspection reports accordingly.
- Manage transactions related to Lot Release within designated systems.
- Collaborate closely with Quality Engineers, Manufacturing, and Process Engineering teams to address Lot Release issues.
- Ensure compliance with operating procedures and complete all required training before performing assigned tasks.
- Monitor equipment condition to verify cleanliness and safe operation.
- Verify that documentation and labeling are clear, accurate, and compliant with Good Manufacturing Practices (GMP).
- Assist in establishing the Lot Release Department and its associated laboratory.
- Support test method validations (TMVs) and troubleshoot testing procedures.
- Initiate and contribute to the Nonconforming Material Report (NCMR) process during commercial product manufacturing.
- Uphold GMP, safety policies, and company standards at all times.
- Perform additional duties as assigned.
Qualifications and Skills
- Level 6 qualification in Quality, Engineering, or related discipline.
- Between 4 to 6 years of experience in the medical device industry.
- Strong interpersonal and team collaboration abilities with proficient verbal and written communication skills.
- Flexibility to work varying shifts to meet operational demands.
- Desirable skills include proficiency with statistical software (e.g., Minitab) and Microsoft Office applications (Word, Excel, Outlook).
Benefits and Opportunities
- Exposure to pioneering continuous glucose monitoring (CGM) technology impacting lives worldwide.
- Comprehensive employee benefits plan.
- Worldwide career progression prospects.
- Access to professional development programs and tuition reimbursement.
- A dynamic, innovative company devoted to employees, customers, and community engagement.
Additional Information
Travel requirements are minimal (0-5%). The annual base salary ranges from €35,445 to €45,870 gross, depending on qualifications and experience. Dexcom is committed to diversity and inclusivity throughout its hiring processes and accommodates applicants needing support related to disabilities. Only applications from individuals are accepted; unsolicited resumes from agencies will not be considered.