Quality Compliance Specialist
Ledgent Tech
Job Description
- No C2C or 3rd Party Candidates will be considered
- Must be local to Southern California as this sits 100% onsite in Tustin, CA
- Pay is $38-41 per hour W2
- 9-12 month contract with possible extension
- Associate degree with 5+ years of medical device industry experience, or a Bachelor's degree in a scientific, engineering, or medical discipline, or ISO Lead Auditor certification.
- Minimum 2-4 years of direct experience in Medical Device Quality Assurance and/or Regulatory Compliance.
- Direct experience handling Class II/Type II medical devices preferred.
- Regulatory Expertise: Deep understanding of FDA 21 CFR Part 820, ISO 13485, and EU MDR.
- Audit Familiarity: Prior experience participating in internal or external regulatory audits.
- Problem-Solving Skills: Strong root-cause analysis capability utilizing tools like 5 Whys or Fishbone diagrams.
- Software Competence: Experience utilizing specialized Electronic Quality Management Systems (eQMS) and electronic databases.
- Computer Skills & Organization: Strong computer skills and excellent organizational abilities required. Proficiency in Microsoft Word, Excel, and PowerPoint is essential, along with the ability to manage multiple tasks, maintain accurate records, and work efficiently in a fast-paced environment.
Job Reference: JN -102026-433095
Vacancy posted 16 hours ago
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