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Expériences
- ETHYPHARMPHARMACEUTICAL CONSULTANTjanvier 2024 - janvier 2025 (1 an)• · Qualification and validation of analytical laboratory equipment, including IQ/OQ/PQ of HPLC systems and UV-Vis spectrophotometers.• · Led the migration and validation of Empower software to version 3.8, ensuring data integrity and regulatory compliance.• · Performed calibration testing, data analysis and deviation investigation.• · Managed equipment troubleshooting.
- GENEXPATHQUALITY ASSURANCE AND REGULATORY AFFAIRS SPECIALISTjanvier 2023 - janvier 2024 (1 an)• · Supported the maintenance and continuous improvement of QMS in compliance with ISO 13485 and MDR 2017/745 requirements.• · Reviewed, updated, and maintained QMS procedures, work instructions, and records, ensuring alignment with regulatory and internal standards.• · Actively participated in internal audits and supplier audits, including preparation, execution support, follow-up, and CAPA implementation.• · Managed CAPA processes, including root cause analysis, effectiveness checks, and follow-up actions to ensure continuous quality improvement.• · Handled non-conformities and change control activities, ensuring proper impact assessment and documentation within the QMS.• · Prepared quality performance reports and indicators, providing transparency on quality metrics and supporting management review activities.• · Collaborated closely with Production and R&D teams to ensure quality standards were consistently applied across the organization.
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Formations
- MSC INMSC IN
- BACHELOR OF SCIENCEBACHELOR OF SCIENCE