Export RSS des offres - Seulement les offres à la une : Non / Métier : OPERATIONS / Niveau d'expérience : 1 to 3 years

2026-35075 - System Test Engineer

Fri, 24 Apr 2026 22:02:37 Z

2026-35066 - Junior QC Analyst - Pharma

Fri, 24 Apr 2026 22:02:37 Z

2025-34520 - Reliability Engineer - Industry - M/F/X

Fri, 24 Apr 2026 22:02:35 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
🎯 Assignments : As an Asset & Reliability Engineer, you will support the development and implementation of asset management and reliability best practices across production sites. Your responsibilities will include: Feeding the long-term asset plan with key data to evaluate technical health. Developing and implementing technical health evaluation techniques through preventive maintenance inspections. Modeling asset remaining lifetime and estimating criticality. Performing criticality and Pareto analyses to identify top performance issues. Facilitating root cause analysis (RCA) for major technical failures. Defining and implementing reliability improvement actions in collaboration with technical services. Optimizing preventive maintenance plans by comparing inspections with asset failure data. Translating improvement actions into job instructions, task lists, and SAP updates.

👤 The profile You hold a BSc or MSc in Engineering, with education in reliability engineering or maintenance management, and at least 2 years of experience in reliability engineering. You are fluent in French and English (Dutch is a plus) and have experience with CMMS, preferably SAP. Autonomous, proactive, and a strong team player, you thrive in multi-team environments and communicate effectively across disciplines. Experience in the chemical process industry is an advantage.
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-33946 - EI&C Engineer - Energy Sector - M/F/X

Fri, 24 Apr 2026 22:02:34 Z

Métier : OPERATIONS/ENGINEERING/PRODUCTION
Contrat : CDI
Description du poste :
We are looking for an I&C Engineer to design and develop Distributed Control System (DCS) architectures and control-command systems for nuclear power plants. Your responsibilities will include: Designing DCS architectures and control-command systems tailored for nuclear power plants. Conducting studies for the selection, supply, and installation of instruments. Drafting technical specifications for DCS, control-command systems, and associated instruments. Performing functional analyses, creating flowcharts, and conducting studies on interlocks and regulation loops. Designing and implementing hardware/software interfaces between control-command systems and field equipment. Preparing tender documentation and assessing technical and commercial proposals. Managing contracts and overseeing the construction, installation, and testing processes at both factory and site levels. Participating in and leading commissioning activities.

Educational Background: Master’s degree in Electromechanical Engineering with a specialization in automation, or an equivalent qualification. Industry Knowledge: Solid understanding of power plant processes, with additional knowledge of nuclear power plants considered a valuable asset. Systems Engineering Expertise: Familiarity with Systems Engineering principles related to Instrumentation and Control (I&C) equipment and the lifecycle of control systems. Technical Proficiency: Strong knowledge of control-command systems and their various applications. Language Skills: Bilingual in French and English, facilitating effective communication in diverse environments. Willingness to Travel: Open to international assignments and geographically flexible, allowing for adaptation to various project locations and requirements. Candidate Profile: A combination of technical expertise and interpersonal skills that positions you as a strong candidate for roles in the energy sector.
Lieu : Brussels and Liège

2024-32166 - FPGA Engineer

Fri, 24 Apr 2026 22:02:28 Z

Métier : OPERATIONS/ENGINEERING/PRODUCTION
Contrat : CDI
Description du poste :
Akkodis è un leader globale nel mercato dell'ingegneria e della ricerca e sviluppo, che mira ad accelerare l'innovazione e la trasformazione digitale utilizzando la forza dei connected data. Con la passione per la tecnologia e il talento, il gruppo, composto da più di 50.000 ingegneri ed esperti digitali e con un fatturato di €4bn, offre una profonda esperienza intersettoriale in 28 paesi tra Nord America, EMEA e APAC. Akkodis vanta un’esperienza quarantennale e un forte know-how in settori tecnologici chiave come la mobilità, i servizi software e tecnologici, la robotica, i test, le simulazioni, la sicurezza dei dati, l'intelligenza artificiale e l'analisi dei dati. In Akkodis crediamo nel valore della diversità, dell’equità e dell’inclusione. Ci impegniamo ogni giorno a costruire un ambiente di lavoro in cui ogni persona possa sentirsi accolta, rispettata e valorizzata, indipendentemente da età, genere, abilità, esperienza, cultura, orientamento sessuale, religione, disabilità o background socioeconomico. Tutte le nostre offerte di lavoro sono aperte anche a persone con disabilità, in conformità con la Legge 68/99, e il nostro obiettivo è garantire un processo di selezione equo, accessibile e rispettoso delle esigenze individuali. Per offrirti la migliore esperienza possibile durante il percorso di candidatura, ti invitiamo a segnalarci eventuali necessità specifiche legate alla tua disabilità, così da poter predisporre i giusti supporti e garantire un’interazione serena e inclusiva. La combinazione di competenze informatiche e ingegneristiche porta a un'offerta unica di soluzioni end-to-end, con quattro linee di servizio - Consulting, Solutions, Talents e Academy - per supportare i clienti nel ripensare ai loro processi di sviluppo prodotto e di business, migliorare la produttività, ridurre al minimo il time-to-market e dare forma a un domani più smart e sostenibile. La divisione Aerospace and Defence di Akkodis è leader nei servizi ingegneristici per le industrie aerospaziale, difesa, navale e ferroviaria. Composta da un team di ingegneri e consulenti altamente qualificati, con una solida esperienza in progetti complessi, la divisione garantisce soluzioni innovative negli ambiti di progettazione e sviluppo di sistemi, integrazione e collaudo, gestione della supply chain, supporto alla certificazione in conformità alle normative militari e civili. Grazie a collaborazioni con importanti attori del settore ed a un costante aggiornamento sulle tecnologie emergenti, Akkodis è in grado di fornire un supporto completo e personalizzato per affrontare le sfide del mercato globale. Nell’ottica di un potenziamento della divisione per progetti ad alto contenuto tecnologico, ricerchiamo una figura di: FPGA Engineer La nostra forza è da sempre l’integrazione delle nostre competenze, che ci permettono di avere una visione a 360° del mondo ingegneristico, presente in Italia e nelle altre Region Mondiali, con collaborazioni tra team.

Quale sarà il tuo contributo in Akkodis? Inserito all'interno di un team multidisciplinare, ti occuperai dello sviluppo di una nuova architettura e versione di FPGA destinata ad applicazioni mission-critical in ambito Aeronautico e Difesa. In particolare, le tue attività comprenderanno: Gestione dell'intero ciclo di sviluppo firmware (FW) per dispositivi FPGA, dalla raccolta dei requisiti all'implementazione. Progettazione, sviluppo e validazione di circuiti logici complessi ad alta affidabilità. Scrittura e ottimizzazione di codice RTL utilizzando il linguaggio VHDL. Esecuzione di simulazioni e test di verifica per garantire la conformità agli stringenti standard dei settori Aerospace & Defence. Integrazione e collaudo a livello di sistema, collaborando a stretto contatto con i team hardware e software. Hai una Laure Specialistica/Magistrale in Ingegneria Elettronica, Ingegneria delle Telecomunicazioni o cultura tecnica equivalente. About you Requisiti per iniziare il tuo percorso di crescita: Esperienza pregressa di almeno 1 anno in attività di progettazione e sviluppo FPGA/Firmware. Ottima padronanza del linguaggio di programmazione VHDL. Solida conoscenza dell'intero ciclo di sviluppo FW per FPGA e dei relativi tool di sintesi e simulazione. Comprovata capacità di progettare architetture e circuiti logici complessi. Ottima conoscenza della lingua inglese (scritta e parlata), essenziale per l'interazione in contesti internazionali e la stesura di documentazione tecnica. Disponibilità alla mobilità geografica per brevi trasferte in ambito nazionale e internazionale. Completano il profilo spiccate doti di problem solving, attitudine al team working, proattività, orientamento al risultato e forte autonomia nell'organizzazione dei task assegnati. Offerta Contratto a tempo indeterminato Cosa troverai in Akkodis? Un percorso di carriera strutturato e personalizzato, con possibilità di crescita verticale e trasversale Ti supporteremo grazie ai nostri piani di formazione, ad una performance review annuale, ad un affiancamento nelle fasi iniziali di ingresso, unitamente a follow-up con figure Manageriali e HR Business Partner. Avrai a disposizione una Piattaforma di Corporate Benefits. Location Torino / Milano / Pisa / Roma
Lieu : Torino / Milano / Pisa / Roma
Niveau d'études minimum requis : 6. Bac +5 / Master

2024-31708 - Supply Chain Planner - Life Sciences - M/F/X

Fri, 24 Apr 2026 22:02:27 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About Akkodis : Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. Akkodis is part of the Adecco Group. Our Webstite : www.akkodis.com Contexte : Akkodis recherche un Suply chain planner pour l'un de ses clients pharmaceutiques. L'approvisionnement des produits repose sur un réseau de plus de 50 CDMO (Contract Development and Manufacturing Organizations) et 4 sites de production internes. Le Supply Network Planner gère les opérations de la chaîne d'approvisionnement pour certains de ces sites, en optimisant la planification (MPS), la gestion des performances, des capacités et des inventaires. Il travaille en étroite collaboration avec les équipes de fournisseurs et différentes fonctions internes de la chaîne d'approvisionnement. Ce rôle, nécessitant parfois des déplacements internationaux, rapporte directement au responsable du réseau d'approvisionnement pour le portefeuille DP & Devices de Global Supply Chain. Vos principales missions : - Planification de la production (MPS) : Élaborer et mettre en œuvre des plans de production viables sur un horizon de 18 mois ou plus, en utilisant les outils OMP+ et SAP, et coordonner avec les partenaires de production. - Gestion de la distribution et de la logistique : Assurer que les plans de production respectent les exigences des clients et les politiques de stock, et collaborer avec la Global distribution pour gérer les opérations quotidiennes. - Analyse et gestion des performances : Surveiller et analyser les performances d'approvisionnement à travers des KPI définis, mener des analyses de causes profondes et faciliter les discussions sur les performances avec les partenaires. - Planification des capacités : Développer des vues de capacité pour les sites de production, participer aux cycles SIOP et aux projets d'extension de capacité. - Résolution des problèmes d'escalade : Gérer les problèmes d'approvisionnement escaladés et informer les parties prenantes des impacts et des solutions proposées. - Intégration de la planification : Intégrer les entrées aux plans d'approvisionnement, soutenir la planification de scénarios et résoudre les problèmes d'approvisionnement. - Amélioration des processus et des systèmes : Contribuer à l'amélioration des processus et systèmes de la chaîne d'approvisionnement, proposer des initiatives d'amélioration continue. - Partenariat et collaboration : Établir des relations de confiance avec les représentants de la chaîne d'approvisionnement des sites de production et participer activement aux réunions des équipes fournisseurs. - Innovation et digitalisation : Soutenir les initiatives d'innovation et de digitalisation en collaboration avec les équipes Global Supply Chain. - Gestion des risques : Assurer la gouvernance de la gestion des risques pour le réseau CDMO et proposer des mesures de mitigation.

Vous êtes : - Titulaire d'un bachelier or d'un master - Avec un background en opérations pharmaceutiques et/ou une expérience en planification, avec des compétences techniques dans les processus de fabrication associés étant un plus. - Des compétences en systèmes SAP/OMP - Un esprit analytique, axé sur les KPI et les résultats. - L'anglais oral et écrit est primordial pour ce poste. - Capacités démontrées en planification et en gestion des contraintes. - Capacité d'apprendre rapidement dans un environnement complexe. - Personne rigoureuse, capable d'avoir une vue d'ensemble et une vue très détaillée. - Une certification APICS fundamentals est un plus Pourquoi vous ne pouvez pas refuser cette offre ? En tant que membre de l'équipe AKKODIS, vous serez : - Embarqué dans votre fonction via un processus de buddy process - Accompagné dans votre carrière par votre Business Manager - Acteur de votre plan de formation et de votre développement personnel et professionnel - Bénéficiant d'un contrat à durée indéterminée - Bénéficiant d'un package salarial compétitif incluant plusieurs avantages extra-légaux.
Lieu : Brabant-Wallon
Niveau d'études minimum requis : 5. Bac +3 / Bac +4
Langue / Niveau :
Anglais : 3 : Courant - Confirmé

2026-35143 - System Software Engineer - Automotive

Fri, 24 Apr 2026 09:49:22 Z

Métier : OPERATIONS/ENGINEERING/PRODUCTION
Contrat : CDI
Description du poste :
Akkodis è un leader globale nel mercato dell'ingegneria e della ricerca e sviluppo, che mira ad accelerare l'innovazione e la trasformazione digitale utilizzando la forza dei connected data. Con la passione per la tecnologia e il talento, il gruppo, composto da più di 50.000 ingegneri ed esperti digitali e con un fatturato di €4bn, offre una profonda esperienza intersettoriale in 28 paesi tra Nord America, EMEA e APAC. Akkodis vanta un’esperienza quarantennale e un forte know-how in settori tecnologici chiave come la mobilità, i servizi software e tecnologici, la robotica, i test, le simulazioni, la sicurezza dei dati, l'intelligenza artificiale e l'analisi dei dati. La combinazione di competenze informatiche e ingegneristiche porta a un'offerta unica di soluzioni end-to-end, con quattro linee di servizio - Consulting, Solutions, Talents e Academy - per supportare i clienti nel ripensare ai loro processi di sviluppo prodotto e di business, migliorare la produttività, ridurre al minimo il time-to-market e dare forma a un domani più smart e sostenibile. La divisione Automotive e Transportation è in prima linea nello sviluppo dei veicoli software-defined vehicles, guidando l’innovazione verso requisiti, operazioni e funzionalità completamente gestite da software. Forniamo soluzioni avanzate per la connettività dei veicoli, attraverso lo sviluppo di infrastrutture, il monitoraggio intelligente, l’IoT e l’architettura cloud, senza dimenticare l’ attenzione alla sicurezza informatica nello sviluppo di applicazioni end-to-end. Nell’ottica di un potenziamento del team, ricerchiamo un: System Software Engineer - Automotive Entra a far parte della nostra divisione Automotive e Transportation, un gruppo di oltre 300 consulenti che operano in Italia e circa 8.000 a livello globale. La nostra forza è da sempre l’integrazione delle nostre competenze, che ci permettono di avere una visione a 360° del mondo Auto. Quale sarà il tuo contributo in Akkodis? Lavorerai su centraline di controllo veicolo in pre-produzione, occupandoti di programmazione, debug e integrazione tra software, elettronica e sistema fisico. Svolgerai l'attività su veicolo reale e analisi guasti su ECU, segnali e cablaggi. Attività: Sviluppo e modifica software per ECU veicolo e HMI in C, Python, e Codesys Debug su veicolo integrato, analisi difetti e ricerca causa radice Troubleshooting su logiche di controllo, segnali I/O e cablaggi Test e verifica centraline anche su banco prova Integrazione tra ECU, attuatori e interfacce utente Analisi reti veicolo tramite CAN / CANalyzer Collaborazione con team System, Test, Software e fornitori.

Profilo Hai una Laurea Magistrale in Ingegneria Elettronica, dell'Automazione, Meccatronica o Informatica ed hai maturato almeno 1 anno di esperienza in gestione software per sistemi di controllo o automazione? Potrai entrare nel team Automotive e Transportation, seguire progetti diversi e completare la tua formazione universitaria. About you Requisiti per iniziare il tuo percorso di crescita: buona conoscenza di Vector Canalyzer gradita conoscenza di C, Python e Codesys esperienza con sistemi HW/SW integrati e gestione segnali l'esperienza in Automotive e l'utilizzo di Canalyzer saranno un plus ottime capacità comunicative, collaborative e relazionali Conoscenza fluente della lingua inglese e italiana. Offerta Tempo indeterminato 💼 Cosa troverai in Akkodis? Un percorso di carriera strutturato e personalizzato, con possibilità di crescita verticale e trasversale Ti supporteremo grazie ai nostri piani di formazione, ad una performance review annuale, ad un affiancamento nelle fasi iniziali di ingresso, unitamente a follow-up con figure Manageriali e HR Business Partner Avrai a disposizione una Piattaforma di Corporate Benefits Sede di lavoro Provincia di Parma In Akkodis crediamo nel valore della diversità, dell’equità e dell’inclusione. Ci impegniamo ogni giorno a costruire un ambiente di lavoro in cui ogni persona possa sentirsi accolta, rispettata e valorizzata, indipendentemente da età, genere, abilità, esperienza, cultura, orientamento sessuale, religione, disabilità o background socioeconomico. Tutte le nostre offerte di lavoro sono aperte anche a persone con disabilità, in conformità con la Legge 68/99, e il nostro obiettivo è garantire un processo di selezione equo, accessibile e rispettoso delle esigenze individuali. Per offrirti la migliore esperienza possibile durante il percorso di candidatura, ti invitiamo a segnalarci eventuali necessità specifiche legate alla tua disabilità, così da poter predisporre i giusti supporti e garantire un’interazione serena e inclusiva.
Lieu : Provincia di Parma
Niveau d'études minimum requis : 6. Bac +5 / Master

2026-34958 - System Requirements Engineer

Thu, 23 Apr 2026 22:01:59 Z

2026-34938 - Project Engineer Water - Energy - M/F/X

Thu, 23 Apr 2026 22:01:59 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role As Project Engineer Water, your role is pivotal in designing major marine infrastructure projects, ensuring high-quality and standards-compliant solutions for complex water-related structures. The position involves technical design responsibilities, multidisciplinary coordination, client interaction, and project follow-up from concept to completion. You will lead the design of assigned components within large marine infrastructure projects and act as a technical point of contact for various stakeholders, including clients, joint venture partners, engineering consultancies, subcontractors, and contractors. Key responsibilities Lead the design of components within large marine infrastructure projects, ensuring compliance with standards Act as a technical point of contact for clients and partners, facilitating effective communication Produce designs for port master planning, locks, quay walls, jetties, and other structures Analyze and optimize installation methods, exploring innovative solutions Coordinate and coach engineers and CAD designers, verifying drafting work

About you Master of Science in Structural Engineering with a focus on marine engineering Proficient in Dutch, with good knowledge of English or French At least 2 years of relevant design experience in marine infrastructure Strong knowledge of Belgian and European standards and public sector contract management Experience with SCIA Engineer, Plaxis, GeoStudio, or DSheet Piling is a plus
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-34687 - Project Engineer Experimental Pilot plant (EPP) - Life Sciences - M/F/X

Thu, 23 Apr 2026 22:01:58 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role This service will be employed in EPP (experimental pilot plant), a non-GMP lab. This service will work hands-on in the lab and will be responsible for the experimental set-up and simulation of various production steps in the drug product manufacturing process. This serves to design a robust commercial production process to ensure timely supply of the sterile injectable medicines to patients. You will work in a group with about 25 colleagues focused on all kinds of process design activities in a high-tech environment. In addition, as a team member you are also responsible for the proper functioning of the lab, including safety and 5S.

About you Masters degree, preferably with a first proven laboratory experience Able to thrive within a fast changing environment Good communication skills (written and oral) Excellent knowledge of English and basic understanding of Dutch Knowledge of statistics and a pharmaceutical background is a plus
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-34686 - Project Engineer Utilities Validation - Life Science - M/F/X

Thu, 23 Apr 2026 22:01:58 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role The Utilities team is responsible for executing projects from design to final delivery (basic and detailed design, procurement, construction, start-up, and validation). The utilities supplied to the production process mainly consist of clean utilities (direct impact compressed air, clean steam, water for injection, nitrogen) and black utilities (steam, city water, cooling water, nitrogen, vacuum, etc.). As a Project Engineer Utilities Validation, you acts as a point of contact for validation within the Utilities team. You will prepare and review all validation documents and provide support to several Project Engineers across multiple projects. In addition, you actively works on validation optimization and ensures that evolving regulations are implemented. Systems such as MIR, CAPA, and CRF are familiar to you, as you will regularly work with them and ensure that no overdue actions remain assigned to the Utilities team. Key responsibilities Act as the main point of contact for validation within the Utilities team. Support project engineers with all validation-related documentation. Define a clear validation strategy from the start of each project. Prepare a detailed validation planning aligned with the overall project or operational planning. Contribute to quality improvement initiatives. Build expertise to act as a Subject Matter Expert (SME). Ensure accurate and compliant documentation. Take ownership of small-scale projects and follow them up independently.

About you Excellent command of Dutch and English. Strong communication and administrative skills. Well-organized and accurate working style. Knowledge of GMP principles. Technical knowledge of utilities systems is a plus.
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-34684 - Project Engineer Utilities - Life Sciences - M/F/X

Thu, 23 Apr 2026 22:01:58 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role The engineering department is responsible for executing diverse projects, with the Project Engineer Utilities serving as the point of contact for utilities technology within these projects. The role encompasses managing projects from design to final delivery, focusing on clean utilities such as compressed air, clean steam, water for injection, and nitrogen, as well as black utilities like steam, city water, cooling water, nitrogen, and vacuum. The utilities may involve generation, storage, and distribution. Key responsibilities Serve as the primary contact for the utilities scope of the project Develop functionality and P&ID specifications to meet client expectations Conduct risk analyses and ensure accurate documentation Coordinate and oversee installation, verification, and validation testing (FAT/SAT) Lead project planning aligned with general or operational timelines for timely delivery

About you Higher technical education (industrial, civil or bioengineer) Proficiency in Dutch and English for effective communication Strong analytical and problem-solving skills in process engineering Ability to lead and motivate a project team independently Detail-oriented with excellent organizational and administrative skills Experience in piping process engineering, with a minimum of 1 to 5 years
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-34580 - CSV Engineer - Life Sciences - M/F/X

Thu, 23 Apr 2026 22:01:58 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role This role involves ensuring compliance with cGMP standards through the validation of computerized systems. You will be responsible for developing and executing validation studies, generating documentation, and maintaining the validated status of systems. This position requires hands-on involvement and technical expertise in validation processes. Ideally, you have experience in the pharmaceutical sector and a strong understanding of quality and compliance regulations Key responsibilities Develop, implement, and execute validation studies for cGMP-critical computerized systems, regarding URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities Generate validation documentation and assist with protocol execution for computerized systems Ensure validated status of systems complies with cGMP standards at all times Manage projects in accordance with Sanofi and cGMP regulatory standards Provide technical assistance on US FDA and EU validation requirements

About you Strong communication skills for effective collaboration and reporting Ability to work independently and adapt quickly to new challenges Competent knowledge of Computer Systems Validation processes Full understanding of relevant quality and compliance regulations Minimum of 3 years of experience in the pharmaceutical sector and GMP environment
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-34499 - Operations Advanced Supervisor - Life Sciences - M/F/X

Thu, 23 Apr 2026 22:01:57 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role As supervisor, you will manage a team of approximately 30 members, including process operators, cleanroom leads, badge record reviewers and experts. Responsibilities include overseeing daily operations, conducting one-on-one and evaluation meetings, participating in recruitment interviews, and collaborating with schedulers for planning. The position operates on a 4/4 shift system with 10-hour shifts. Key responsibilities Manage operational teams and supervise various units within the CAR-T production process Ensure strict compliance with cGMP standards and manage quality aspects Collaborate with other departments to resolve production issues effectively Oversee and review critical documentation such as procedures and work instructions Supervise the release and review of batch records for quality control

About you Preferably a PhD or Masters degree in science, bio-engineering, pharmacy or other related fields Min 3 years of experience in a GMP or ATMP environment (preferably within the pharmaceutical or biotech industry) Knowledge regarding cGMP regulations and clean room operations is an advantage Familiarity with MES (Manufacturing Execution Systems) & ERB (Electronic Batch Record) is a plus You are fluent in English (spoken & written)
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-34486 - Quality project associate - Life Sciences - M/F/X

Thu, 23 Apr 2026 22:01:57 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role As a Quality project associate, you will ensure product quality and compliance within Quality Operations. The position involves overseeing product-related qualifications and validations, ensuring regulatory Chemistry, Manufacturing & Controls (CMC) compliance, and facilitating successful product launches. The specialist will act as an independent quality authority, focusing on validation, registration, and implementation processes. This is an opportunity to contribute to the excellence of product launches and regulatory compliance in a dynamic environment Key responsibilities Act as the quality authority for product-related qualifications and validations, ensuring compliance with cGMPs Oversee process qualification, method validation, and component qualification for assigned products Ensure regulatory CMC compliance by reviewing registration dossiers and site practices Conduct data verification and QA review for marketing authorization filings and variations Implement approved regulatory changes timely and accurately across different markets

Your Skills Possess a Master's degree in a scientific discipline such as Pharmacy or Biomedical Sciences Min 2 years of experience in the pharmaceutical or medical device industry Excellent analytical and problem-solving skills in a quality assurance context Exhibit strong oral and written communication skills in both Dutch and English Maintain a thorough understanding of cGMP, regulatory guidances, and medical device regulations
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-34485 - Business Analyst - Life Sciences - M/F/X

Thu, 23 Apr 2026 22:01:57 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role We are seeking a Business analyst with expertise in industrial automation and software development. This role involves managing multiple projects within a Scrum framework, providing UX/UI guidance, and performing Computer Systems Validation (CSV) and Computer Systems Assurance (CSA) activities. The candidate will have a strong analytical mindset and the ability to work independently while collaborating with external parties on process automation projects. This position requires excellent communication skills in Dutch and English and offers the opportunity to work in a dynamic environment focused on innovation and efficiency. Key responsibilities Monitor project scope, objectives, and planning within a Scrum framework Provide UX/UI expertise and guidance on ongoing projects Perform Computer Systems Validation (CSV) and Computer Systems Assurance (CSA) activities Define test scenarios and express them using Gherkin syntax Draft qualification protocols and participate in software testing, including headless applications Conduct risk assessments Provide second-line support during daily operations

About you Master’s or Bachelor’s degree in Computer Sciences or Automation, or equivalent experience Minimum of 3 years of experience in an industrial automation environment Minimum of 3 years of experience in software development Strong analytical skills, structured mindset, and innovative thinking Experience in writing functional specifications and executing automation projects Fluent in Dutch and English (verbal & written)
Lieu : Noordkustlaan 16B 1702 Dilbeek

2025-34482 - Project Engineer Building Electricity & Safety - Life Sciences - M/F/X

Thu, 23 Apr 2026 22:01:57 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the rol This role involves working on projects that focus on the development and maintenance of electricity systems, including low and high voltage, network infrastructure, gas monitoring systems, and lighting. Additionally, the position encompasses security systems such as CCTV, access control, and fire detection. The Project Engineer collaborates with the Technical Owner to find optimal solutions that balance quality and budget, with a strong emphasis on safety. Key responsibilities Collaborate with multidisciplinary team to align project scope, planning and budget Guide third-party contractors in the execution of project tasks and responsibilities Prepare detailed technical specifications and scope of work documents Manage the sourcing and appointment of contractors, coordinating with procurement as needed Oversee contractor activities and ensure compliance with project requirements

About you Master's degree in electrical or electromechanical engineering VCA certification for supervisors, knowledge of Caneco software and experience with drawing tools (Eplan or AutoCAD) A first experience in the pharmaceutical industry and/or demonstrable experience working with electricity/security at an industrial level is a plus Fluency of Dutch and English
Lieu : Noordkustlaan 16B 1702 Dilbeek

2024-33155 - Automation Engineer - Life Sciences - M/F/X

Thu, 23 Apr 2026 22:01:53 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About Akkodis Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis offers broad industry experience, and strong know-how in key technology sectors such as mobility, software & technology services, robotics, testing, simulations, data security, AI & data analytics. The combined IT and engineering expertise brings a unique end-to-end solution offering, with four service lines – Consulting, Solutions, Talents and Academy – to support clients in rethinking their product development and business processes, improve productivity, minimize time to market and shape a smarter and more sustainable tomorrow. Akkodis is part of the Adecco Group. Our Webstite : www.akkodis.com Description du poste / Rôle -Vous coordonnez et contrôlez des projets d’automation -Vous assurez la mise en service de nouvelles installations -Vous participez aux projets de conception, de développement et de maintenance de commandes automatisées -Vous assurez la programmation d’automates industriels du type Siemens, ABB, Schneider, Delta V, OsiPi OU Rockwell -Vous gérez et coordonnez les équipes / sous-traitants sur le terrain -Vous assistez à la SAT / commissioning / validation. -Vous signalez et gérez les risques de façon proactive. -Vous passez en revue les protocoles de vérification. -Vous organisez les formations des opérateurs. -Vous soutenez les activités de mise en service

Vos compétences : -Vous disposez d'un master avec une orientation technique (ingénieur en électronique, informatique, automatisation) -Vous disposez d'au moins 5 ans d’expérience en automatisation ( Expérience avec Siemens indispensable, Delta V est un plus) -Vous avez déjà été impliqué dans d’importants projets d’ingénierie, y compris la gestion des risques/ obsolescence programmée Bon avez un bon niveau de français et d’anglais -Vous avez des connaissances en environement en GMP/ cGMP Capacité à travailler dans un environnement très dynamique et à gérer des situations difficiles -Excellentes compétences de communication (leadership, négociation, gestion du changement) -Capacité à prendre des décisions d’équipe et sens aigue des responsabilités
Lieu : Brabant-Wallon
Langue / Niveau :
Français : 4 : Expert - Bilingue
Langue / Niveau :
Anglais : 2 : Intermédiaire

2024-32975 - Software Analyst Engineer

Thu, 23 Apr 2026 22:01:52 Z

2026-35097 - Compliance Engineer - Life Sciences - M/F/X

Wed, 22 Apr 2026 22:01:54 Z

Métier : OPERATIONS/CONSULTING
Contrat : CDI
Description du poste :
About the role As Compliance Engineer, you will strengthen the Reliability and Support team within the Engineering & Maintenance department. You will focus on ensuring that engineering and maintenance activities are aligned with internal procedures and external requirements that apply to the pharmaceutical industry. You will work with the QMS system (VeeVa), analyze deviations across a wide range of technical systems, and support the implementation of corrective and preventive actions. The role requires frequent interaction with production, QA, and system owners, as well as a strong focus on quality upskilling and monitoring quality-related KPI within the E&M department. Key responsibilities Take responsibility for drawing up actions in the QMS system (VeeVa) within the Engineering & Maintenance department and ensure timely follow-up of all related activities. Act as the central contact person in the Engineering & Maintenance department for performing analyses into the technical root cause of deviations across various technical systems. Perform structured investigations into deviations related to diverse systems, including process systems, HVAC, clean utilities such as WFI, ROW, and process gassenn, ensuring accurate documentation of findings. Support the drafting of any CAPAs, ensuring that corrective and preventive measures are clearly defined, technically sound, and aligned with quality and compliance requirements. Contribute actively to quality upskilling within the E&M department by sharing insights from deviation analyses and supporting continuous improvement of quality awareness.

About you Excellent communication skills Good knowledge of legislation within the pharmaceutical industry, allowing correct interpretation and application of regulatory and compliance requirements in daily work. Experience with Quality Management Systems, ideally including practical use of systems such as the QMS system (VeeVa) in a technical or engineering environment. Background in a compliance-oriented role, providing familiarity with deviation handling, CAPAs, documentation standards, and quality audits in the pharmaceutical context. Ability to work effectively within the Reliability and Support team and the broader E&M department, collaborating on technical root cause analyses and quality upskilling initiatives.
Lieu : Noordkustlaan 16B 1702 Dilbeek