(CONFIDENTIELLE)

About the Company

Confidentielles est le média féminin leader sur les réseaux sociaux : 1,9 M de fans très engagés, 89% d'audience féminine, 5,9 M de visites par mois, 300k followers sur Instagram. Confidentielles a pour ambition de proposer un contenu qualitatif, divertissant et inspirant. La beauté, le style et l’art de vivre y accompagnent les caractères bien trempés de nos millions de lectrices. L’ambiance ? Un média feel good rempli d’inspiration et de conseils pour les femmes aux vies multiples et débordantes d’activités. Confidentielles accompagne également des marques féminines dans leur stratégie de Brand Content en leur proposant ponctuellement ou à l'année des contenus inspirants, à fort engagement social.

Listed Jobs

Company Name

(CONFIDENTIELLE)

Job Title

Ingenieur verification RTL senior F/H

Job Description

**Job Title**: Senior RTL Verification Engineer **Role Summary**: Develop and verify communication systems between user interfaces and electronic components, including SoC/FPGA devices. Focus on firmware, embedded software, and RTL design to ensure seamless integration and functionality across hardware-software interfaces. **Expectations**: - Proficiency in Python, C/C++ embedded, or VHDL. - Strong collaboration within cross-functional teams. - Adaptability to evolving project requirements. **Key Responsibilities**: - Design and develop firmware for PC (Python) and microcontroller (C) communication programs. - Implement RTL design (VHDL) for FPGA companion chip functionality. - Contribute to hardware design specifications for future NanoXplore boards. - Deliver tools and documentation to clients. - Provide technical support to internal teams and end-users. **Required Skills**: - Advanced knowledge of **Python** or **C/C++ embedded development**. - Experience with **VHDL** for digital design. - Proficiency in **GNU/Linux command-line tools** (Makefile, shell scripting). - Familiarity with **JTAG debugging** and **OpenOCD** for hardware testing. - Strong understanding of **I2C, USB, PLL, and voltage/current monitoring** protocols. - **Git** version control expertise. - Prior open-source project experience preferred. **Required Education & Certifications**: - Bachelor's or Master's degree in **Electrical/Electronic Engineering**, **Computer Science**, or **Applied Physics**. - No certifications required.

Hauts-de-seine, France

On site

Senior

10-10-2025

Company Name

(CONFIDENTIELLE)

Job Title

Ingenieur automaticien/Ingenieure automaticienne Lyon F/H

Job Description

Job Title: Automation Engineer Role Summary: Execute and manage automation projects for pharmaceutical clients, from design to commissioning, ensuring compliance with industry regulations. Expectations: Deliver technically sound automation solutions, maintain supplier relationships, and provide clear documentation in English. Work independently while coordinating multidisciplinary teams. Key Responsibilities: - Coordinate automation projects and manage procurement, contracts, and vendor interactions - Design, develop, test, and maintain automated systems and equipment - Program PLCs (Siemens Step 7 and TIA Portal) and supervise systems (TIA Portal, SCADA, GAMP‑compatible) - Oversee the installation and commissioning of new plant installations - Create and review technical documentation, including specifications, test plans, and validation reports Required Skills: - Proficiency with Siemens PLCs (Step 7, TIA Portal) and supervisory software (TIA Portal, SCADA) - Strong knowledge of GMP, BPF, GAMP, and 21 CFR Part 11 regulatory frameworks - Ability to read, write, and translate technical documentation in English - Excellent communication, organization, and stakeholder‑management skills Required Education & Certifications: - Bachelor’s or Master’s degree (BAC+5) in Automation Engineering or related field - Minimum 3 years of industry experience in pharmaceutical automation

Rhône, France

On site

16-10-2025

Company Name

(CONFIDENTIELLE)

Job Title

Ingenieur V&V (Validation & Verification) Lyon F/H

Job Description

**Job title**: Validation & Verification Engineer (Consultant) **Role Summary** Provide expert validation and verification support for medical device projects. Draft functional specifications for automation systems, design test strategies, create and execute test protocols, and manage non‑conformities to ensure regulatory compliance and product quality. **Expectations** - Minimum 2 years of V&V experience in the medical device industry. - Strong understanding of Human‑Machine Interfaces (HMI). - Prior software engineering experience. - Proficient in English, both written and spoken. **Key Responsibilities** - Write functional specifications for automation hardware and software. - Develop comprehensive test strategies aligned with regulatory standards. - Author detailed test protocols and test plans. - Execute functional, integration, and system tests. - Log, analyze, and track non‑conformities; coordinate corrective actions. - Collaborate with design, development, and quality assurance teams. **Required Skills** - Functional specification drafting - Test strategy and protocol development - Test execution and defect management - HMI design and validation - Software testing fundamentals - Regulatory knowledge (ISO 13485, IEC 62304, FDA 21 CFR Part 820) - Excellent written and verbal communication in English **Required Education & Certifications** - Bachelor’s or Master’s degree from an accredited engineering program. - Certifications in software testing or medical device validation (e.g., ISTQB, CQP, or equivalent) preferred.

Rhône, France

On site

16-10-2025

Company Name

(CONFIDENTIELLE)

Job Title

Ingenieur V&V (Validation & Verification) Paris F/H

Job Description

**Job Title:** Validation & Verification Engineer **Role Summary:** Consultant responsible for performing validation and verification activities on medical device software. Duties include drafting functional specifications, defining test strategies, creating and executing test protocols, and handling non‑conformities while ensuring compliance with industry standards. **Expectations:** - Minimum 2 years of V&V experience in the medical‑device sector. - Engineering degree from an accredited institution. - Strong background in software development. - Proficiency with Human‑Machine Interfaces (HMI). - Fluent oral and written English. **Key Responsibilities:** - Write functional specifications for automation systems. - Develop comprehensive test strategies and detailed test protocols. - Execute functional, integration, and system tests. - Identify, document, and manage non‑conformities. - Collaborate with client teams to ensure compliance and quality. **Required Skills:** - V&V methodologies and best practices. - Knowledge of medical device regulations (e.g., ISO 13485, IEC 62304). - Software development and testing expertise. - Experience with HMI design and validation. - Defect tracking and root‑cause analysis. - Strong written and verbal communication in English. **Required Education & Certifications:** - Bachelor’s or Master’s degree in Engineering (e.g., Electrical, Mechanical, Software, or Biomedical). - Relevant certifications in medical‑device quality or V&V (optional but advantageous).

Paris, France

On site

16-10-2025