Clinical Compliance Operations Specialist

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1 hour ago
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Full time
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documentation gcp iso 9001 gxp csv
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📋 Description

  • Facilitate GCP audits and project implementations
  • Review GxP and QA records and remediation efforts
  • Document audit findings and drive CAPA actions
  • Author GxP docs and records to promote compliance
  • Lead process improvements and incident management
  • Provide quality oversight on regulated activities and product releases

🎯 Requirements

  • Bachelor’s degree or equivalent
  • 3+ years in Clinical QA in Life Sciences
  • Experience with Quality Management Systems (documentation, CSV, investigations, CAPA)
  • Knowledge of ISO 9001 or GCP/QSRs
  • Strong technical writing and communication skills

🎁 Benefits

  • Note: Compensation ranges provided in local currency
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