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QA Inspector 2

Dexcom

QA Inspector 2

Dexcom

Penang, Malaysia

·

On-site

·

Full-time

·

1mo ago

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.

Meet the team:

As a member of the QA Lot Release team, the inspector is responsible for ensuring the activities related to

the inspection functions in a manner which meets company standards and methods as determined by

quality assurance or other engineering departments.

Where you come in:

  • You perform in-process and final product review of documents for accurate format, signatures, dating, and Good Documentation Practices (GMP) for commercial products in a timely manner.

  • You perform in-process product inspection and testing to ensure commercial products conform to specified requirements in accordance with product specifications and quality assurance standards.

  • You prepare, record, and update inspection report forms.

  • You maintain compliance with operating procedures and ensure training is completed prior to performing any task.

  • You ensure all documentation is legible, complete, and correct per current Good Manufacturing Practices and inspect labeling for finished products.

  • You apply approval or rejection labels to lots/products after completing inspection data review and lot history record (LHR) verification.

  • You initiate and assist with the NCMR process during manufacturing of commercial products.

  • You demonstrate good computer skills and perform operations to generate reports and graphs using Microsoft Word and Excel.

  • You review shipping documentation to ensure accurate order shipment.

  • You compile and update regular inspection reports.

  • You monitor equipment and instruments to ensure they are clean and safe to use.

  • You use Microsoft Suite products: Word, Excel, and Outlook.

  • You adhere to all GMP, safety guidelines, and company standards at all times.

  • You assume and perform other duties as assigned.

What makes you successful:

  • You have a high school certificate (SPM) or equivalent, with a minimum of 2 years of relevant industry experience and/or training.

  • You demonstrate good interpersonal and teamwork skills.

  • You must be able to flex your schedule to work different shifts to meet demand.

  • You have experience in Quality Assurance and/or QA/QC.

  • You have at least 2 years of experience in the medical device or manufacturing industry.

  • You ideally have experience working with Cloud PLM, Oracle, and/or Camstar software programs.

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: (Highlight the appropriate range)

  • 0-25%

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.

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About Dexcom

Dexcom

Dexcom develops, manufactures, and distributes continuous glucose monitoring systems for diabetes management.

10,001+

Employees

San Diego

Headquarters

$13.2B

Valuation

Reviews

4.1

10 reviews

Work Life Balance

3.8

Compensation

4.2

Culture

4.0

Career

4.1

Management

3.7

78%

Recommend to a Friend

Pros

Great team and people to work with

Good compensation and benefits

Positive work environment and culture

Cons

Growing pains and organizational changes

Large company processes and structure

Leadership and management challenges

Salary Ranges

292 data points

Senior/L5

Senior/L5 · Data Analyst

0 reports

$159,250

total / year

Base

-

Stock

-

Bonus

-

$135,362

$183,138

Interview Experience

5 interviews

Difficulty

2.6

/ 5

Duration

14-28 weeks

Offer Rate

20%

Experience

Positive 40%

Neutral 20%

Negative 40%

Interview Process

1

Application Review

2

Recruiter/HR Screen

3

Phone/Technical Screen

4

Hiring Manager Interview

5

Panel/Leadership Interview

6

Offer

Common Questions

Behavioral/STAR

Technical Knowledge

Past Experience

Culture Fit

Role-Specific Skills