QA Inspector 2
Core
Perform in-process and final product inspection, testing, and documentation review for commercial continuous glucose monitoring (CGM) devices to ensure compliance with quality standards and Good Manufacturing Practices (GMP).
Role type
QA Inspector (Medical Device Manufacturing)
Builds
Commercial CGM products for diabetes management
Domain
Medical device manufacturing / Biosensing technology
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
In-process and final product inspection, GMP compliance, documentation review and formatting, lot history record verification, equipment monitoring, Microsoft Office Suite (Word, Excel, Outlook), shipping documentation review
Preferred skills
Cloud PLM, Oracle, Camstar software experience, Quality Assurance/QC background
Responsibilities
Perform in-process and final product review of documents for format, signatures, and GMP compliance; Perform in-process product inspection and testing to ensure conformity to specifications; Prepare, record, and update inspection report forms; Apply approval or rejection labels to lots/products after inspection data review; Initiate and assist with the NCMR process during manufacturing; Monitor equipment and instruments to ensure cleanliness and safety; Review shipping documentation for accuracy.
Seniority
Entry-level to Mid-level, hands-on IC