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Compliance Specialist

2 months ago


Temecula, United States GForce Life Sciences Full time

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