Supervisor QC Inspection
at Dexcom
Athenry, County Galway, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jan, 2025 | Not Specified | 19 Oct, 2024 | 5 year(s) or above | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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.
Our Quality Assurance team are looking for a dynamic and skilled Incoming Inspection Supervisor to support the start-up of our first European manufacturing site in Athenry. In this role, you will plan and direct the activities related to the inspection function in a manner which meets company standards and methods as determined by Quality Assurance or other engineering departments. You will outline and implement training procedures of employees for the inspection operation including drawings, prints, schematics and quality assurance standards. You will take an active role in making recommendations for capital expenditures and manpower in the inspection area as well as selecting and developing personnel to ensure the efficient operation of the function.
Where you come in :
- You will p erform supervisory and administrative duties associated with inspection resource management.
- You will c oordinate the tasks and work plans of the receiving inspection area.
- You will o bserve and verif y the accuracy and adequacy of the inspection activities and records.
- You will be r esponsible for material flow, storage of parts, and accurate inventory transactions within the MRP system.
- You will m aintain quality metrics and reports, as required , and implement appropriate prevent at ive/corrective action to improve quality.
- You will identify potential issues and propose resolutions that are timely , cost-effective, and meet quality requirements.
- You will identify and implement continuous improvement projects.
- You will a ssist in the development of inspection procedures.
- You will be r esponsible for supporting inspection of engineering builds.
- You will w ork across sites to ensure alignment of Product Release Activities
- You will c onduct training for receiving inspection team.
- You will w ork with QA, Manufacturing, Engineering, and other department personnel, as necessary, to support quality and business objectives .
- You will as sume and perform other duties as assigned.
What makes you successful :
- Typically requires a Bachelor’s degree with 5-8 years of industry experience. Informal management/ team lead experience.
- You have e xperience in medical device or equivalent regulated industry
- You have a m inimum of 3 years applying quality management systems
- You understand acceptance sampling plans, ANSI/ASQ Z1.4, Z1.9 and C=0.
- You can read and understand specifications and inspection criteria and to apply criteria using appropriate and properly configured inspection tools.
- You are a self-motivated individual, able to work in a team with minimal supervision.
- You have s trong computer skills desired; proficient in use of Microsoft Office and database applications. Oracle and SolidWorks experience preferred.
- You have strong written and verbal communication skills.
What you’ll get :
- A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community .
- A full and c omprehensive benefit s progra m .
- Growth opportunities on a global scale.
- Access to career development through in-house learning programs and/or qualified tuition reimbursemen t.
- A n exciting and innovative , industry - leading organization committed to our employees , customers , and the communities we serve .
TRAVEL REQUIRED:
- 5 -10 %
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
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:5.0Max:8.0 year(s)
Information Technology/IT
Production / Maintenance / Quality
Software Engineering
Graduate
Proficient
1
Athenry, County Galway, Ireland