Caduceum

www.caduceum.fr

2 Jobs

324 Employees

About the Company

Caduceum : L’expert 100% santé pour accélérer vos projets industriels Depuis 2013, Caduceum s’impose comme LE partenaire de référence pour les acteurs des industries de la santé. Filiale spécialisée Life Sciences du groupe ALTEN, nous accompagnons les industriels pharmaceutiques, biotechnologiques, du MedTech, vétérinaires, cosmétiques et nutrisanté. Notre mission ? Concevoir, industrialiser et optimiser vos produits, de l’idée à la mise sur le marché. Notre force ? Une expertise pointue et une approche sur-mesure, portée par plus de 400 collaborateurs passionnés qui interviennent sur toute la chaîne de valeur : Compliance & Qualité : Conformité et excellence opérationnelle Engineering & Manufacturing : Solutions innovantes et industrialization de vos produits IT & Digital : Transformation numérique et optimisation des processus. Affaires Réglementaires & R&D : Accompagnement stratégique et innovation. Notre petit truc en + qui fait toute la différence ? Une Direction Technique européenne, composée de plus de 200 ingénieurs, et 3 pôles d’excellence pour répondre aux enjeux les plus complexes, nous permettant de combiner agilité, innovation et expertise sectorielle pour offrir des solutions efficaces et scalables. Notre objectif ? Co-construire ensemble des solutions durables et innovantes, adaptées à vos défis industriels et réglementaires. Envie d’en savoir plus ? Découvrez comment nous pouvons accélérer vos projets : www.caduceum.fr #LifeSciences #Caduceum #ALTEN #Innovation #ExpertiseSanté #Ingénierie #Qualité #IndustriePharma #Manufacturing

Listed Jobs

Company Name: Caduceum
Job Title: Ingénieur V&V (Vérification et Validation) – Dispositifs Médicaux F/H
Job Description: **Job Title:** Verification & Validation Engineer – Medical Devices (F/M) **Role Summary:** Provide consultant‑level verification and validation services for medical device projects, including drafting functional specifications, developing test strategies, authoring test protocols, executing tests, and managing non‑conformities. **Expectations:** - Produce accurate functional specifications for automation systems. - Design and implement comprehensive test strategies and plans. - Execute functional, integration, and regression tests. - Track, document, and resolve non‑conformance items. - Maintain rigorous V&V documentation and audit trails. - Communicate effectively in English with engineering, QA, and regulatory teams. **Key Responsibilities:** - Draft functional specifications for automation/control systems. - Define test strategy and create test plans in compliance with medical device standards. - Write detailed test protocols and test cases. - Execute functional, integration, and regression tests. - Track, report, and manage non‑conformance issues and corrective actions. - Maintain V&V documentation and audit trails for regulatory review. - Collaborate with cross‑functional teams (engineering, QA, regulatory). **Required Skills:** - Minimum 2 years’ experience in V&V for medical devices. - Proficiency with Human‑Machine Interface (HMI) design and validation. - Strong software engineering and testing background. - Excellent written and spoken English. - Documentation, test planning, and defect tracking expertise. - Detail‑oriented, analytical, and independent work capability. **Required Education & Certifications:** - Bachelor’s or Master’s degree in Engineering or a related field.

Company Name: Caduceum
Job Title: Ingénieur Automaticien F/H
Job Description: Job Title: Automation Engineer (Ingenieur Automaticien) – Male/Female Role Summary Design, implement, and maintain industrial automation solutions for pharmaceutical manufacturing. Coordinate automation projects, manage supplier relationships, program Siemens PLCs, and ensure compliance with health‑sector regulations. Expactations - Minimum 3 years of industrial automation experience in a pharmaceutical setting. - Strong command of Siemens Step 7 and TIA Portal PLC programming. - Proficiency with SCADA or TIA Portal supervisory systems. - Comprehensive understanding of GMP, BPF, GAMP, and 21 CFR part 11 requirements. - Ability to read, create, and translate technical documentation in English. - Excellent communication, rigor, and organizational skills. Key Responsibilities - Lead automation projects from scope to completion, coordinating cross‑functional teams and suppliers. - Design, develop, and troubleshoot PLC‑based processes and integration with MES/SCADA systems. - Conduct commissioning and validation of new installations, ensuring adherence to regulatory standards. - Maintain and upgrade legacy automation equipment and software. - Draft technical specifications, functional documentation, and validation reports. - Provide training and support to plant operators and maintenance staff. Required Skills - Siemens PLC programming (Step 7, TIA Portal) - SCADA/TIA Portal system integration - Pharmaceutical process knowledge (filtration, fill‑pack, sterile operations) - Regulatory compliance (GMP, BPF, GAMP, 21 CFR part 11) - English technical writing and documentation - Project management and supplier coordination - Analytical, problem‑solving, and detail‑oriented mindset Required Education & Certifications - Bachelor’s or Master’s degree (Bac+5) in Automation Engineering, Electrical Engineering, or related field. - Professional certification in Siemens PLC programming preferred. - Knowledge of GMP/GAMP training or certification advantageous.