Clinical Compliance Operations Specialist

📋 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