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%