Abdelkader HALLAL

Ingénieur Validation Logiciels Médicaux Senior

Salaire / Taux journalier

Paris, France

Freelance

Peut venir sur site

Expertises

Test & QA

Langues

Anglais

À propos

Introduction

Medical software validation engineer with 10+ years of expertise in healthcare applications and web app qualification. Proven track record in V&V for pharmaceutical dosage guides, dental imaging software, and medical devices compliance. Specialized in quality assurance, test automation, and regulatory documentation for CE registration and ISO compliance.

Liens

Expérience de travail

Web App Qualification Engineer

Ipsen

sept. 2020 - Présent

6 ans 2 mois

Paris, France

Goals: Dosing Guide Dysport: Validation of a Web application for a dosage guide, intended for the treatment of Spasticity and Spasmodic Torticollis: Achievements:  Write the validation plan, risk analysis, test scripts, validation reports for CE registration.  Review of functional and technical specifications and of the Post-Market surveillance plan.  Management of non-conformities with the team.  Participate in project points and ensure project compliance.  Participate in the execution of tests.  Support on changes to the Lumen App (iOS & Android): Updating the Lumen application following anomalies detected among users:  Help on the documentation of changes on the Lumen application (Non DM)  QMS Digital Medical Devices  Analysis of the gap between the existing IT QMS and the need for ISO compliance for Medical Devices  Proposal for an action plan Technical environment (s):  System: iOS, Android, Windows and Linux  Technical Environment: Jira, Easidoc, Box, ServiceNow  Software version management tool: Jenkins Git  Methodology: Agile (Scrum)

Software Quality Assurance Engineer

Carestream Dental

mars 2016 - oct. 2020

4 ans 8 mois

Région de Paris, France

Goal :  Validation and Verification of Intra & Extra_Oral dental imaging software (Panoramic, Cephalometric, RVG, CR, Camera 2D & 3D). Achievement (s):  Analysis of specifications.  Specification of test procedures  Definition of the test coverage matrix  Carry out the test campaigns.  Reporting and monitoring anomalies detected during the tests  Management of anomalies by business expertise  Writing test reports Technical environment (s):  System: Windows and Linux  Language: UFT QTB, Cucumber.  Quality Center (ALM11), TestTrack, Caliber, TargetProcess  Software version management tool: Jenkins Git  Methodology: Agile (Scrum)

COMMAND CONTROL ENGINEER- V&V CONTROL-COMMAND TEAM-

AREVA NP

mars 2014 - mars 2016

2 ans 1 mois

Région de Paris, France

The mission consists of verifying and validating the code of safety controllers for EPR type nuclear power plants (Flamanville, Olkiluoto and Taishan) Tasks:  Specify the test procedures to validate the PLC code  Carry out the test campaigns under simulator  Support the teams carrying out the platform test campaigns  Expertise the anomalies detected during the tests  Respond to customer requirements and requests for changes  Costing of activities according to the client's model  Analysis of project specifications, concepts and constraints  Definition of the test coverage matrix  Specification of test procedures  Realization of test robots in Python  Execution of test procedures under simulator  Support for the execution of platform tests  Management of anomalies by business expertise  Writing test reports  Meeting with the client for presentation of the works, convergence and delivery  Respect of budgets (time / costs) Technical environments:  System: Windows and Linux  Language: Python, VBA-Excel  Tools: Cassis, Notepad ++, SynaptiCAD / Timing Diagram Pro  Software version management tool: Mercurial / TortoiseHg

SOFTWARE VALIDATION ENGINEER

EOS imaging

janv. 2014 - mars 2014

3 mois

Région de Paris, France

The mission is to test and validate a medical imaging interface, which can diagnose osteoarticular diseases (hip, knee, back) and orthopedic surgeries. Tasks:  Write the verification / validation procedures for an Orthopedic application.  Execution of verification campaigns and validation of the SterEOS software.  Verification of compliance of computer equipment (HW Verification + Report)  Writing test procedure from specifications  Review of functional specifications  Software defect follow-up and verification of corrections made  Write the verification / validation procedures for an Orthopedic application, CPACS synchronization.  Participate in the verification and validation campaigns of the SterEOS 1.6 & 1.7 software Technical environments:  Windows (XP, 7).  Excel, Word.  Mantis, Ennov

SOFTWARE VALIDATION ENGINEER

GE Healthcare

juil. 2012 - déc. 2013

1 an 6 mois

Région de Paris, France

The mission consists of testing and validating a software for processing medical images and assisting in the diagnosis of all modalities (CT, MR, PET, XA, etc.) This software is used in pre and postoperative analysis but also in the hospital room. operation for some of these vascular protocols, like the one I was responsible for. (Synchro3D / Innova) Tasks:  Write the verification / validation procedures for a Cardiovascular application, CPACS synchronization.  Participate in the verification and validation campaigns of the Volume viewer software.  Work within the project team  Workload management and distribution on the team  Verification of compliance of computer equipment (HW Verification + Report)  Writing test procedure from specifications  Tests on vascular, cardiac, pulmonary applications (including writing test reports)  Review of functional specifications  Improvement of an Excel invoicing / reporting tool  Software defect follow-up and verification of corrections made  GE quality and technical training (followed by e-learning)  Communications written entirely in English. Technical environments:  Linux / Windows  AW / Volume Viewer  DOORS

MEDICAL SOFTWARE INTEGRATION TEST ENGINEER

Carmat

juin 2011 - juil. 2012

1 an 2 mois

Région de Paris, France

The mission consists in verifying the integration of the various modules constituting the medical software system, ensuring the management of the communication of a console with an implantable artificial heart, as well as the supply of the prosthesis, the monitoring of the physiological data of the patient, in a hospital environment. Management of all project operations. Tasks:  Development and design of test tools.  Writing of test procedures to verify the compliance, vis-à-vis the requirements defined upstream, of the components: Test, User, Patient, Parameters, Alarms and Constraints.  Review and verification of procedures carried out for other modules.  Execution of test campaigns.  Software defect follow-up and verification of corrections made Technical environments:  LabVIEW, DOORS (Requirements and traceability management software), SVN  Microsoft Office (Excel, Word).  Database data management, Postgres SQL tools.  Anomaly tracking systems: Mantis Bug Tracker  Windows (XP, 7)


Formation

Pierre and Marie Curie University

Master's degree

2008 - 2010

2 ans 1 mois

Ecole Nationale Polytechnique

ELECTRONIC ENGINEER

2005 - 2008

3 ans 1 mois

NATIONAL PREPARATORY SCHOOL FOR ENGINEERING STUDIES

UNDERGRADUATE SCIENTIFIC DIPLOMA

2002 - 2005

3 ans 1 mois

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