Freelancer profile translated to English.

Description

I help small business leaders transition from manual, scattered, and time-consuming management to an automated system that works for them and frees up their time.

After 9 years in large international groups — Continuous Improvement, R&D, Quality, Packaging — I understood one thing: their real strength is not their talent. It's their systems:

- Centralized data for better decision-making.

- Decades-refined processes.

- Automations that trigger the right actions at the right time.

The whole thing runs on its own — for consistent results, regardless of the people in place.

Conversely, many small businesses juggle spreadsheets and tools that don't talk to each other — and copy the same information in 5 different places, leading to errors and wasted time.

This is the imbalance I've chosen to address. Thanks to No-code tools, I now help human and creative professions build their own systems: simple, automated, and truly useful on a daily basis.

Industry field of expertise

Languages

Chinese
Native or bilingual
French
Fluent
English
Fluent

Workplace preferences

Can work on-site

Lyon (up to 50km)

Capgemini Engineering
Consultant Engineer
PHARMACEUTICALS INDUSTRY
June 2021 - October 2025 (4 years and 4 months)
Assignment at Sanofi, Marcy-l'Étoile
- Support for two Sanofi Marcy L'Etoile departments in data migration related to the Learning Management System (LMS) change.
- Preparation of the necessary structure for data migration.
- Testing and verification of the accuracy of data samples in accordance with GxP requirements.

Assignment at Rockwell, Jonage
- Management of the change control process and coordination between the client and automation testers for the implementation of modifications.
- Training of automation testers in quality processes: FAT/SAT execution, change control procedures, etc., in accordance with GxP and Data Integrity requirements.
- Review of quality documents for PREFAT, FAT, and SAT phases in the pharmaceutical industry, as well as writing associated reports.

Assignment at Sanofi, Marcy-l'Étoile
- Management of changes to vaccine packaging data (labels, inserts, boxes, needles, etc.) in the SAP system in accordance with local Regulatory Affairs requirements, ensuring compliance with supply chain deadlines and production line specifications.
- Analysis of requests and entry of reliable data into SAP for Computer-Assisted Publishing (CAP) and production of packaging components.
Quality Assurance Data Migration Data Analysis
Groupe SEB
Innovation Research Project Manager
September 2018 - April 2021 (2 years and 7 months)
Graduate Program in R&D – SEB Group

• 1st assignment
-> Creation of new concepts for garment steamers (Research Center at headquarters, Écully)
Innovation project management: generation of innovative concepts; exploration of technical solutions; collaboration with design, marketing, and quality teams, subcontractors; prototype testing and improvement

• 2nd assignment
-> Sensor testing for air purifiers (Supor, China)
Design and execution of performance tests to evaluate the feasibility of digitizing formaldehyde detection in an air purifier, according to Chinese standards.
Testing and evaluation of particle sensors to reduce costs.

• 3rd assignment
-> Coatings for cookware (Tefal, Rumilly)
Study and optimization of non-stick coatings: laboratory formulation, material characterization, trial monitoring, performance improvement, and collaboration with production teams.
Project Management Teamwork Product Development
ResMed SAS
Continuous Improvement Engineer
MEDICAL
July 2016 - June 2018 (1 year and 11 months)
Saint-Priest, France
Management of continuous improvement projects with R&D, Quality, Production, and After-Sales Service teams, in compliance with ISO 13485 standard.

Reduction of product return rates through optimization of manufacturing processes (CAD-CAM in 3D printing by laser sintering, vibratory finishing, manual finishing, etc.).

Root cause analysis of non-conformities and implementation of the CAPA process for correction and prevention.

Implementation of quantitative measurement protocols for product quality control.

Execution of IQ/OQ/PQ validations and industrial maintenance of production equipment (3D printer, 2D optical measurement system, etc.).
Continuous Improvement Process Improvement