QA Inspector 2

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:

• 0-25%