• 3+ years of Quality Assurance or Quality Auditing experience within the medical device, pharmaceutical, or healthcare industry
• Hands-on experience conducting quality audits of regulated documentation (product complaints, adverse events, CAPAs, or similar)
• Exceptional attention to detail with the ability to identify documentation errors, inconsistencies, and compliance gaps
• Strong understanding of FDA Quality System Regulations (21 CFR Part 820) and/or ISO 13485
• Excellent written and verbal communication skills with experience presenting audit findings and collaborating across teams
• Proficiency with Ms Office/Excel and quality management/document control systems

Range: $30-33/hr

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.