Role: Medical Device Quality Inspector
Location: San Diego, CA
Duration: 12 months
Key Responsibilities:
Review service records in digital systems (Salesforce, SAP, Excel, etc.) to ensure accuracy and compliance.
Collaborate with internal teams (Service Quality, Field Engineers, Implementation Analysts) to meet project timelines and improve processes.
Identify risks and work with the team to mitigate them.
Monitor compliance with FDA, ISO, and other regulatory standards (CFR 820, BSI, CSA).
Skills & Qualifications:
Technical: Proficiency in Salesforce, SAP, Microsoft Office (Excel, Word, PowerPoint), and document management systems.
Regulatory Knowledge: Familiarity with FDA, ISO 13485, and industry compliance standards (CFR 820, BSI, CSA).
Soft Skills: Strong attention to detail, time management, problem-solving, and communication skills.
Experience: Experience with quality management systems, record review, or audits in a regulated environment.
Education: High School/GED required; some college preferred.
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