Freelancer profile translated to English.
Back to original languageAbout Hamid
Looking for a QA tester?
Do you want to ensure the quality of your software products?
You are in the right place.
I am a QA / tester with over 13 years of experience.
I have worked in various sectors such as medical devices and pharma...
I have collaborated with companies such as Intrasense and ClinSearch...
I can assist you with:
- Setting up the testing strategy
- Writing detailed test plans
- Managing defects and enhancements using tools like JIRA, TestRail, and Squash
- Designing and developing automation scripts
- Configuring and integrating automation tools
- Planning production releases.
I also have knowledge of: Ranorex, Playwright, GitLab, Squash, HP ALM, XRay, TestRail, Postman, Jmeter, SAFe...
I also place great importance on transparency with my clients.
I send a daily report to my clients at the end of the day on all the tasks I have performed.
Do you have a project?
Contact me, I will reply within an hour!
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QA QA test QA engineer QA engineer QA analyst QA mobile QA e-commerce QA testing QA automation lead functional tester tester (QA) Test QA tester Test Test software tester Test lead Tests Tester functional QA tester Software test QA test Automation test consultant QA consultant test
French
Native or bilingual
English
Fluent
Can work on-site
Paris (up to 50km), Lille (up to 50km), Lyon (up to 50km), Toulouse (up to 50km), Marseille (up to 50km)
Experience
- ClinSearchTest Lead EngineerPHARMACEUTICALS INDUSTRYAugust 2021 - Today (4 years and 10 months)Paris, FranceClinsearch is a French CRO specializing in conducting clinical trials for drugs, medical devices, and cosmetic products. With over 25 years of experience, more than 800 projects completed, and studies involving up to 200,000 participants, the company combines clinical expertise with internal digital solutions (EDC, ePRO) to ensure secure data collection compliant with regulatory requirements (GxP, GAMP5).Mission Context:Upon my arrival, no structured software quality process was in place. The initial mission, planned for 6 months, consisted of defining and integrating a testing process compliant with regulatory requirements. Thanks to the value brought, the mission was extended over 4 years with a strong involvement in the continuous improvement of product quality.Key Achievements:• Implementation of the software quality process according to GAMP5 and GxP standards• Development of a risk-based testing strategy to prioritize critical scenarios for the safety and compliance of clinical data.• Selection and deployment of adapted tools:o ALM for requirements and test campaign managemento Ranorex for GUI test automation• Integration of the QA process into the agile development cycle in collaboration with development teams, DevOps, and project managers• Automation of regression tests• Active participation in quality audits (internal and client)Results Obtained:• Significant improvement in deliverable quality: reduction in the number of bugs in production.• Better traceability of requirements, test cases, and results, compliance with standards• Sustainability of the quality processEnvironment: Java - Angular - TypeScript - Java Script - PWA - Oracle DB - JIRA - GitLab - Postman - Ranorex - JMeter - GAMP5
- IntrasenseQA TesterMEDICALSeptember 2012 - December 2020 (8 years and 3 months)Montpellier, FranceIntrasense is a French medtech company specializing in medical imaging software with AI. Founded in 2004 in Montpellier, it has 70 employees and supports over 1,200 facilities in 40 countries with its flagship solutions like Myrian®.Mission Context:With a background in biomedical engineering specializing in medical imaging, I joined Intrasense as a QA to take charge of validating critical functionalities related to automatic organ detection algorithms, measurement tools (metrology), and image display quality.Key Achievements:• Definition and implementation of a testing strategy adapted to the specifics of the medical field and regulatory constraints (CE, FDA).• Development of functional and technical test plans, including the validation of image processing algorithms and measurement tools integrated into the application.• Use of digital phantoms (synthetic medical images) to verify the accuracy of measurements and the behavior of algorithms in extreme or rare cases.• Automation of critical scenarios via Ranorex, integrated into CI/CD• Management of test campaigns in collaboration with development, clinical validation, and regulatory teams.• Active participation in the preparation of regulatory submission dossiers, particularly for CE/FDA/SFDA certification.Results Obtained:• Improved robustness and compliance of critical modules.• Clear, traceable validation documentation compliant with regulatory authorities' expectations during audits and submissions.• Sustainability of a quality methodological framework within R&D teams.Environment: C# - VB - Git - Matlab - Jenkins - Ranorex - HP Quality Center - Azure Devops - DICOM
- LISTR&D EngineerMEDICALJanuary 2012 - July 2012 (6 months)LuxembourgEnvironment: Clinical research, telemedicine, post-stroke monitoring, scientific writing, functional specificationsThe CAPSYS project, led by LIST in Luxembourg, aimed to develop an innovative telemedicine device for the home monitoring of stroke patients. This intelligent system, combining connected objects and data analysis, was designed to detect early signs of relapse and proactively alert healthcare professionals.Mission Context:As part of the project launch, I joined the multidisciplinary R&D team to provide scientific, functional, and quality expertise during the initial design phases of the device.Key Achievements:• Writing a scientific state-of-the-art review: in-depth analysis of medical and technological literature on post-stroke monitoring, existing telemedicine solutions, and physiological sensors used at home.• Drafting functional specifications for the device, aligned with identified clinical needs and project technical constraints.• Contribution to the development of Proofs of Concept (PoC): evaluation of sensors, usage scenarios, and the system's functional architecture.• Participation in workshops with clinical stakeholders (doctors, researchers, engineers) to ensure alignment between medical requirements and proposed technological solutions.Results Obtained:• Structuring of the project on solid scientific foundations.• Delivery of clear functional deliverables, facilitating the transition to the development phase.• Strengthening of collaboration between technical and clinical actors around a common goal of secondary stroke prevention.
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Education
- Master of Biomedical EngineeringFaculty of Medicine - Nancy2012- Acquérir des compétences et des connaissances solides en sciences fondamentales, biophysique, électrophysiologie, électronique, informatique, instrumentation et traitements des signaux physiologiques et des images médicales. - Connaître l’environnement professionnel, les méthodes et les technologies du domaine médical, la réglementation, l’imagerie, l’informatique de santé, la maintenance, la démarche qualité. - Gérer et mener à bien des projets multidisciplinaires associant par exemple l’instrumentation, le traitement de signal, l’informatique, la mécanique, la médecine, la biologie, la réglementation, la qualité etc. - Assurer différentes fonctions d’Ingénierie Biomédicale de la conception et développement, au marketing et vente, à l’application, l’installation et la maintenance.
- HND - Physical Technology for Industry and LaboratoryLycée Arthur Varoqaux2009
Certifications
- ISTQB - Foundation levelGASQ2016
- Master of Biomedical EngineeringFaculty of Medicine - Nancy2012