Compliance Specialist

Compliance Auditor

12-month contract

Onsite in Temecula, CA

Responsibilities:

• Perform quality system and manufacturing process audits
• Prepare audit report that establishes the outcome of the audit and the detail of non-conformances identified during the audits
• Track audit results including corrective actions, and follow up to these actions as required
• Support Third party and regulatory agency inspection as required
• Provide support to SQA team as needed

Qualifications:

• Bachelors Degree in related field i.e.. science or engineering
• previous audit experience within the medical device industry relating to ISO 13485 and FDA regulations for medical devices
• 3-5 years of experience within the medical device industry
• CQA preferred