RSS export of vacancies - Only featured vacancies : No / Profile : OPERATIONS-->CONSULTING, SUPPORT-->FINANCE

2026-35260 - Calibration Engineer - Automotive

Thu, 25 Jun 2026 22:04:21 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
🎯 Assignments We are looking for an Calibration Engineer to join one of our clients in the automotive sector, specialising in electric and hybrid powertrain development. Your main responsibilities include: Executing calibration work packages using dedicated equipment and established processes Fine-tuning parameters, validating control strategies, and optimising the performance, efficiency, and reliability e-Drive systems Defining and conducting test plans to calibrate and validate e-Drive systems across various operating conditions and test setups (e-Drive test bench, transmission test bench, chassis dynamometer, vehicle) Performing drivability assessments, both objective and subjective, supported by data acquisition systems Managing calibration datasets for assigned software modules Collaborating across disciplines to remove roadblocks and keep projects on track Exchanging expertise with customers, service providers, and teammates across multiple locations

👤 The profile Background You hold a Master's degree in Electrical, Electro-Mechanical, or Electronics Engineering, or equivalent, with a strong interest in the automotive industry. A valid EU driver's licence (category B) is required. Must Have 2 to 5 years of experience as a powertrain calibration and/or controls engineer, with a focus on e-Drive systems (EV or hybrid vehicles) Solid knowledge of e-Drive systems: electric motor fundamentals, power electronics, sensor integration and calibration, motor control algorithms, and thermal management Awareness of safety requirements related to high-voltage systems in electric and hybrid vehicles Strong automotive background with good understanding of powertrain dynamics Proficiency with block diagrams and Matlab/Simulink Experience with calibration tools and data acquisition systems (e.g. Vector CANape, ETAS INCA) Nice to Have Customer-focused, collaborative, and solution-oriented mindset Comfort working in multi-site, multicultural environments Experience with structured problem-solving methodologies 🌍 Working environment at Akkodis Direct link with a Business Manager for personalised support Technical training to develop your skills Career prospects in a stimulating environment A corporate culture focused on safety, quality, and innovation 🔎 Our recruitment process Stage 1: Initial telephone interview (15 min) with @Kenny, Talent Acquisition. Step 2: Interview (60 min) with a Business Manager. Step 3: Interview (60 min) with the client.
Location : /

2025-34649 - Qualification & Validation Engineer - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:20 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role This role involves the development, implementation, and execution of validation activities for small-scale equipment and related software. The successful candidate will conduct validation studies for cGMP-critical process systems, ensuring compliance with cGMP, user, and regulatory requirements. This position requires hands-on involvement in qualification of systems, interpreting industry standards, and maintaining compliance with cGMP, cGLP, and specific procedures. You will also provide technical assistance on current US FDA and EU validation requirements, ensuring projects align with all necessary regulatory standards Key responsibilities Develop, implement, and execute URS, SIA, DQ, IQ, OQ, PQ, RV, and TM activities for equipment Conduct validation studies to demonstrate compliance with cGMP and regulatory requirements Perform qualification of systems, interpreting standards to specific cases Ensure systems maintain qualified status in compliance with cGMP at all times Provide technical assistance on US FDA and EU validation requirements

About you Strong knowledge of cGMP requirements in a regulated environment Understanding of relevant quality and compliance regulations Ability to troubleshoot validation issues effectively Proficiency in quality management systems Experience in qualification of small-scale equipment and related software
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34404 - Project Engineer Lab operations (tech transfer) - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role: De afdeling Lab Operations is verantwoordelijk voor release testing van de primaire verpakkingsmaterialen, grondstoffen en actieve ingrediënten, het testen van process intermediaren en na afvulling kwaliteitscontrole van afgewerkte producten en stabiliteitsstudies. De kandidaat is verantwoordelijk voor transfer/validatie en implementatie van analytische testmethodes. De kandidaat is sterk in project planning, is een expert in chemisch analytische en bio-analytische technieken, het risico in projecten in te schatten, en een meester in troubleshooting (DMAIC). Key responsibilites: Compliance assessment van methodevalidatie dossiers Compendial compliance assessment Zorgvuldige implementatie van nieuwe testmethodes en procedures in de bestaande Quality Control Operaties Coordinatie & planning van eigen projectactiviteiten Schrijven/review van protocols, test scripts en methodevalidatie/transfer-rapporten + deviaties Review validatie-transfer testen/testresultaten Validatie van rekenfiles (excel, SoftMaxPro,..), nodig voor uitvoering van de analytische methode Verificatie van compendial methodes Eindverantwoordelijk voor een zorgvuldige implementatie van nieuwe testmethodes en procedures in de bestaande QC Operaties Training/Support van QC analisten tijdens uitvoering van de analyses Troubleshooting van issues, special + common cause root cause analysis mbv DMAIC Co-Authoring van registraties van nieuwe medicijnen (BLA, CTD, ..)

About you: Wetenschappelijke opleiding ((industrie) apotheker, bio-ingenieur chemie/cel- en genbiotechnologie, industrieel ingenieur chemie/biochemie, analytische chemie, biochemie) Eerste ervaring binnen pharma, quality control, GMP Je beheerst vlot het Nederlands en Engels Job specific skills: Kennis van methodetransfer en methodevalidatie Wetenschappelijk schrijven Root cause onderzoek (DMAIC) Analytisch chemische technieken: TUR, UPLC/HPLC, KF, IR, CE, IEC, SEC, UV, pH, OSM, TOC, ICP-OES, ... Biochemische technieken: slot blot, SDS PAGE, AEX, ELISA, western blot, … Functionele technieken; dimensionele testen, BLEF, tip cap removal force, container closure integrity, .. Moleculaire technieken; qPCR, ddPCR Cell based testing; celcultuur, flow cytometrie(FACS)
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34403 - Project Engineer Temperature and Relative Humidity mapping - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role: For a leading pharma company, we are seeking a Project Engineer specializing in Temperature and Relative Humidity mapping. This role involves a blend of practical and theoretical work, requiring daily interaction with various departments on-site. Key responsibilities: Independently plan, monitor, and execute validation studies for temperature and humidity Provide support to analysts for routine requalification programs and validation of equipment Initiate changes, analyze results, and prepare validation documents such as protocols and reports Lead improvement projects within processes and standard operating procedures Manage TRH projects, including applying change procedures and overseeing deviations

About you: Master's degree in a scientific field such as bioengineering, industrial engineering, pharmacy, biochemistry, or biotechnology, or equivalent experience Proficiency in English, both written and spoken, is required. Dutch is a plus Knowledge of cGMP and RFT Strong interpersonal skills and ability to work effectively in a team Excellent organizational, independent working, and quality-conscious skills Nice to have: First experience and/or knowledge regarding temperature mapping and/or validation Experience within a similar function, quality- or production environment GMP experience
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34351 - Project Engineer HVAC - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role We are seeking a Project Engineer HVAC to join our client's engineering department. This role involves managing the HVAC components of various projects, including cleanroom construction within the pharmaceutical sector. The Project Engineer HVAC will oversee the entire project lifecycle, from feasibility studies to commissioning, ensuring compliance with industry standards. Collaboration with departments such as Production, Maintenance, and Quality Assurance is crucial for successful project execution. The ideal candidate will possess technical expertise in HVAC systems and demonstrate strong communication skills to facilitate cross-departmental cooperation Key responsibilities Manage the HVAC components of projects from feasibility studies to commissioning Collaborate with Production, Maintenance, and QA departments to ensure project success Conduct detailed engineering and validation of HVAC systems for cleanrooms Develop and maintain project documentation, including P&IDs and validation documents Implement GMP, Six Sigma methodology, and risk management tools like FMEA

About you Completion of higher technical education in Industrial or Civil Engineering or equivalent experience Several years of relevant experience with HVAC systems in a similar role Strong communication skills and assertiveness for effective collaboration Ability to multitask and prioritize tasks efficiently within a team environment Knowledge of GMP, Six Sigma methodology, and risk management tools such as FMEA
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34350 - Production Engineer - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role We are seeking a Production Engineer to join the formulation department within a vaccines plant. This role is pivotal in ensuring the technical operations of the department, contributing to the production of vaccines such as Prevenar, Covid, FSME, Neisvac, and RSV. These vaccines play a crucial role in enhancing healthcare and life expectancy globally. As a Production Engineer, you will be the primary technical contact, responsible for addressing and resolving technical challenges, driving process improvements, and managing projects within the department. Key responsibilities Provide operational support by resolving process or equipment issues promptly Drive process improvements to increase capacity and reduce malfunctions Develop and maintain technical and pharmaceutical procedures and work instructions Implement modifications to existing equipment within established deadlines Manage projects including communication, engineering, execution, and evaluation

About you Master’s degree in a scientific field or equivalent experience is required Excellent command of Dutch and English languages is essential Relevant experience in a production or support environment is advantageous Strong analytical skills with a focus on finding solutions and achieving results Ability to maintain oversight across multiple projects and prioritize effectively
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34349 - Project Engineer Transportation and Handling - Life Sciences - F/M/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role We are seeking a Project Engineer to join the Engineering department. This role is integral to delivering investment projects on schedule and within budget, ensuring the robustness and performance of installations for high-quality injectable medicines. The position involves validation testing and comprehensive documentation to demonstrate system suitability. Projects range from initial definition and scoping to production start-up, after which systems are handed over to production. The focus is on process automation and improving logistics processes, including robotization, bottleneck studies, and transport optimization. The Project Engineer will act as the link between suppliers and various departments, ensuring smooth collaboration and efficient goal achievement Key responsibilities Develop and manage project plans for multiple workstreams, ensuring timely completion Identify and mitigate potential risks related to safety, operability, and maintainability Serve as the primary contact for suppliers, aligning project requirements with production departments Draft equipment specifications and concepts for supplier development and oversee installation Ensure timely preparation and delivery of all necessary project documentation

About you Master’s degree in Industrial Engineering, Mechanical Engineering, Civil Engineering, or Bio-Engineering, or equivalent experience Fluent in Dutch and English, with strong communication skills Proven organizational and documentation skills, with a collaborative team player mindset Background in electromechanical engineering is preferred Experience in project management, including stakeholder engagement and equipment validation
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34348 - Project Engineer Filling - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role For a leading pharma company, we are seeking a Project Engineer with specialized expertise in pharmaceutical filling processes. This role involves managing engineering activities related to the installation and operation of filling equipment, including filling lines, isolators, e-beams, washers, tunnels, and cappers. The successful candidate will provide technical input to project teams, ensuring compliance with operational and technical standards. This position requires a deep understanding of engineering design specifications, P&IDs, and electrical diagrams, as well as the ability to oversee construction and implementation processes Key responsibilities Manage project engineering activities related to specific technology and equipment installation Provide technical input and expertise to project teams for your discipline Define and document technical specifications, including engineering design specifications and diagrams Oversee construction, implementation, and functioning of equipment to ensure compliance with specifications Ensure effective project management practices, including schedule and budget control

About you Expertise in pharmaceutical filling processes and sterile environments Proficiency in defining and documenting technical specifications and engineering design Strong project management skills, including stakeholder management and reporting Ability to oversee contractor activities and ensure successful equipment installation Experience in executing engineering tests, verification, and validation processes
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34316 - CSV & DI Squad Lead - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the Role We are currently seeking a CSV & Data Integrity (DI) Squad Lead. In this role, you will co-lead, together with Local Process Owners, the effort to align all CSV and DI initiatives at the site with current industry best practices. This includes the dimension of risk management. Key Responsibilities Provide expert guidance on CSV and DI best practices, ensuring alignment with modern risk-based approaches Oversee multiple projects, including managing external resources (contractors), ensuring timely and effective delivery Ensure quality and regulatory in collaboration with the corresponding QA lead to assure full alignment Lead change management efforts to embed best practices across the organization Coach and mentor Local Process Owners to elevate their knowledge and implementation of industry best practices

About you Strong expertise in CSV and DI within a pharmaceutical manufacturing context Experience with API environments preferred Familiarity with systems such as DeltaV, PI, PCS7 along with practices as effective alarm management In-depth knowledge of FDA and EMA requirements related to CSV and DI Practical experience with risk-based validation and the preparation of validation documentation Proven project management abilities: planning, coordination, and delivery Strong interpersonal and communication skills Experience in leading teams in complex and dynamic environments Skills in coaching, training, and human change management Ability to navigate organizational dynamics and influence without formal authority Fluent in English, both written and spoken, Dutch is a plus
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34315 - Drug Product Development and CMC Leader - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the Role As Drug Product Development (DP) Leader within the CMC team, you will provide drug product development expertise for the further development of the project. You will manage the clinical bulk supply for a late-stage small molecule program (currently Phase 2 – capsule; Phase 3 tablet development in progress). The development and manufacturing activities are outsourced to external service providers (ESPs). In this key role, you will contribute your deep pharmaceutical expertise—especially in solid dosage form development—to drive the success of the project. Key Responsibilities Lead the development and supply of drug product materials in line with the overall CMC and clinical strategy Develop CMC strategy Represent CMC within the project team Align on strategy, planning, activities and ensure effective coordination of CMC team Manage the CMC budget and report updates to the project team Oversee the (bulk) manufacturing of development batches and GMP batches for clinical purposes Analyze formulation and process data, and adapt as needed Monitor capsule and tablet stability studies, refining plans based on findings Prepare, review, and approve CMC documentation for regulatory submissions Manage and liaise with ESPs performing development and manufacturing tasks Review and archive key documentation from ESPs (e.g., protocols, batch records, reports) Collaborate with Quality & Compliance teams to ensure ESPs adhere to cGMP standards Keep the Product Specification File up to date Ensure compliance with internal procedures and procedures and complete mandatory trainings Provide input for due diligence processes when requested

About you Master or PhD in pharmaceutical sciences, chemistry, bio-engineering, or equivalent through experience Minimum of 10 years of relevant experience in a drug product development role Expertise in solid formulation development and experience working with CROs Proven track record in cross-functional collaboration and technical leadership Fluent in English, both written and spoken Strong organizational, interpersonal, and communication skills Pragmatic, hands-on, and solution-oriented
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34299 - Project Engineer Aseptic Ointments - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
We are seeking a motivated and skilled Project Engineer with experience in pharmaceutical manufacturing to support daily operations within a dynamic and regulated production environment (aseptic ointments). This role combines technical leadership with hands-on involvement in project execution – from design through hand-over within cost, time-schedule and functionality. You bring engineering expertise, GMP understanding, and a proactive mindset to support continuous improvement, reliability, and compliance. Key Responsibilities: Operations related: Ensure compliance with GMP guidelines and industrial standards Implement preventive maintenance plans during shutdowns according to the schedule and manage planned corrective repairs Contribute in maintenance/reliability reviews of new projects Execute and follow up on civil/infrastructure work tasks in the production plant Supervise changeover operations for production equipment to ensure an improvement of productivity Coach and motivate onboarding colleagues Support building organizational culture, aligned with the companies Values & Behaviors Other: Execute projects in line with all stakeholders Make sure projects are executed according to life cycle cost and project schedules Apply technical solutions ensuring compliance with HSE regulations Develop and implement projects on-site according to defined standards Share and implement best practices and expertise across the engineering community of our client Key Performance Indicators: GMP and HSE compliance Fulfillment of project targets Meeting site KPI's

Experience: Proven background in Operations Management and Execution Broad functional knowledge Working across departments Skills & knowledge: Understanding of manufacturing process execution Qualification Knowledge of Total Productive Maintenance (TPM) principles and practices General HSE knowledge Familiar and knowledge of relevant tools and systems Able to manage business continuity Fluent in English and Dutch
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34298 - Automation Engineer - Life Sciences - M/F/X

Thu, 25 Jun 2026 22:04:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
We are looking for a Automation Engineer to support utility automation projects, covering process control systems, instrumentation, PLCs, and SCADA. Ideally you will manage projects from specification to commissioning, ensuring integration, automation and support for production utilities. Key Responsibilities: Project Execution & Management: Define requirements, design, and implement new automation systems (PLC, HMI, instrumentation, electrical). Select suppliers, oversee procurement, testing and commissioning of automation projects. Collaborate with internal stakeholders and vendors to deliver automation solutions aligned with compliance and operational standards. Automation & System Integration: Develop HMI (SCADA) solutions in collaboration with partners and internal teams. Conduct engineering reviews (P&IDs, functional specifications). Review and test PLC code (including fail-safe logic and troubleshooting). Ensure seamless integration with the existing industrial automation infrastructure. Support & Maintenance: Provide technical support for automation systems (including on-call duty every six weeks after one year of service). Lead issue resolution during start-up and drive continuous improvement efforts. Ensure compliance with GMP, documentation requirements, and validation standards.

Education & Experience: Bachelor’s or Master’s degree in Industrial Engineering (Automation, Electromechanics) or equivalent through experience. Minimum of 3 years’ experience in an industrial automation setting. Fluent in Dutch and English (spoken and written). Strong organizational and communication skills; team player with a proactive, hands-on mindset. Technical Skills: PLC programming (Siemens S7-300/400/1500). HMI/SCADA platforms (Siemens WinCC, TIA Portal). SQL and data integration in industrial automation environments. Electrical design and commissioning knowledge (E-PLAN, AREI, EN60204). Industrial IT networks and communication protocols (Profibus, Profinet, OPC). Machinery standards and industrial electrical systems (EN60204). Nice to Have: Experience in GMP-regulated industries (pharmaceutical or equivalent). Familiarity with automation validation and documentation standards in regulated industry.
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34558 - Project Manager – Energy – M/F/X

Wed, 24 Jun 2026 22:04:21 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
🎯 Your main responsibilities: • Identify stakeholders and define an engagement strategy • Develop the project plan (scope, cost, timeline, risks, resources) • Structure the team and assign tasks (Work Packages, scheduling) • Monitor progress, manage risks, and make priority decisions • Lead governance bodies (meetings, Steercos, committees) • Manage scope changes and assess their impact • Apply internal project management procedures • Implement a QHSE plan compliant with site requirements • Ensure communication with key stakeholders • Oversee the procurement process (strategy, contracts, invoicing, closure)

👤 Profile sought: 🎓 Civil or industrial engineering degree (Master’s level) 📊 Minimum of 3 years of project management experience in the industrial sector, ideally in nuclear or energy production 🛠️ Proficient in project management tools (MS Project, Primavera) 📅 Excellent organizational skills, attention to detail, and ability to manage priorities 🧠 Strong analytical thinking, ability to synthesize information, and proactive mindset 🤝 Solid interpersonal skills and ability to work in a multidisciplinary team 🗣️ Fluent in French and English — Dutch is a plus 📜 PMI certification is a valued asset
Location : Brussels

2023-27350 - Automation engineer - Life Sciences - M/F/X

Wed, 24 Jun 2026 22:04:06 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
Description du poste / Rôle En tant que membre de l’équipe principale de projet de notre client, l’expert en automatisation relèvera du responsable de l’automatisation. À titre d’expert en matière d’automatisation, il veillera à l’application de bonnes pratiques d’ingénierie et s’assurera de répondre aux attentes et à la stratégie de nos clients pour tous les colis attribués. Description de poste Veiller à ce que les produits livrables soient fournis en temps opportun et alignés sur la planification du projet avec la bonne qualité attendue et selon le budget . Reporting de l’état d’avancement de ses Packages. Être responsable de ses Packages et en étroite collaboration avec la société Automation Integrator. Harmoniser les attentes en matière de conception avec les autres disciplines du projet : process, QA, Q/V, utilities, E&I, etc. Anticiper, gérer et signaler les risques liés à la conception détaillée jusqu’aux lots de validation. Assurer un transfert efficace aux équipes opérationnelles et veiller à ce qu’elles soient formées pour faire fonctionner l’installation automatisée. Participer à la stratégie d’automatisation globale pour (bibliothèque, structure des recettes, philosophie de l’HMI, rapports, stratégie d’alarme, etc.). Assurer le suivi de l’intégrateur d’automatisation et des logiciels du fournisseur pendant l’élaboration et l’exécution. Assister à la SAT / commissioning / validation. Signaler et gérer les risques de façon proactive. Passer en revue les protocoles de vérification. Organiser la formation des opérateurs. Effectuer le transfert à l’équipe opérationnelle et de soutien. Gérer la liste de commandes liées à ses paquets. Soutenir les activités de mise en service

Vos compétences Master en ingénieur ou licence scientifique (électronique, informatique, automatisation) Au moins 5 ans d’expérience en automatisation des processus (expérience PCS7 indispensable) Implication avérée dans d’importants projets d’ingénierie, y compris la gestion des risques/atténuation Niveau goof de français et d’anglais Solide connaissance des cGMP Solides connaissances en conception, exécution et C&V Capacité de traduire et de présenter les préoccupations des experts pour faciliter la prise de décisions Capacité à travailler dans un environnement très dynamique et à gérer des situations difficiles Excellentes compétences de communication (leadership, négociation, gestion du changement, animation) Capacité à prendre des décisions d’équipe et sens aigu des responsabilités Contact informations YAHIA CHERIF Anissa – Talent Acquisition Officer AKKODIS 0493/31.25.81 – anissa.yahia-cherif@akkodis.com
Location : Brabant Wallon, Hainaut
Language / Level :
French : 4 : Native / Bilingual level
Language / Level :
English : 3 : Advanced

2026-35301 - System Engineer – Embedded & Communications Systems

Wed, 24 Jun 2026 10:36:46 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
Role Overview We are looking for a System Engineer to contribute to the design, integration, and validation of complex systems involving communication, radar, or embedded technologies. You will work at the crossroads of system design, engineering disciplines, and integration, ensuring that technical solutions meet performance, reliability, and operational requirements. Key Responsibilities Analyze and formalize system and network requirements based on project needs Design and define system architectures, including hardware and software components Contribute to the integration of communication and network equipment into complex systems Create, manage, and maintain system requirements using Model-Based Systems Engineering (MBSE) practices Collaborate with multidisciplinary teams (electronics, mechanical, software) on system design and integration Support integration, verification, validation, and qualification (IVVQ) activities Investigate technical issues, perform root cause analysis, and implement corrective actions Act as technical focal point for specific subsystems or workstreams Ensure traceability and consistency of system requirements and documentation

Required Profile Degree in Engineering (electronics, electromechanics, computer science, or similar) 1 to 5 years of experience in system engineering or system design Experience in embedded systems, communication systems, or complex technical environments Familiarity with Model-Based Systems Engineering (MBSE) approaches Strong analytical and problem-solving skills Ability to work in multidisciplinary teams and complex environments Proactive mindset with strong ownership and accountability Technical Skills Experience with MBSE tools such as Capella, Enterprise Architect, or similar Familiarity with requirement management tools (e.g., DOORS, Jira, or equivalent) Knowledge of system engineering standards and methodologies (e.g., INCOSE, MBSE frameworks) Understanding of system documentation (e.g., specifications, interface documents) Networking & Systems Knowledge Knowledge of network architectures and protocols (TCP/IP, DHCP, DNS, VLAN, serial communication) Understanding of telecom systems, sensor integration, or communication technologies Awareness of cybersecurity principles and secure system design is a plus Integration & Validation Experience or exposure to Integration, Verification, Validation, and Qualification (IVVQ) processes Ability to support system testing and validation activities Familiarity with system lifecycle and development processes Nice-to-Have Experience in regulated or high-reliability environments Exposure to embedded systems, real-time systems, or signal processing Knowledge of complex system integration (vehicle, aerospace, industrial systems, etc.) Familiarity with industry standards or certification frameworks Key Competencies Strong communication and collaboration skills Structured and detail-oriented approach Ability to manage complexity and multiple interfaces Critical thinking and problem-solving mindset Adaptability and willingness to learn Language Skills Good command of English (professional working proficiency) Additional languages are a plus
Location : Belgium

2026-35300 - Senior Business & Project Analyst – AI & Intelligent Automation

Wed, 24 Jun 2026 10:34:32 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
Role Overview We are looking for a Senior Business and Project Analyst with strong expertise in Intelligent Automation and Artificial Intelligence. In this role, you will act at the intersection of business and technology, driving initiatives that leverage AI and automation to improve efficiency, innovation, and operational performance. You will play a key role in translating business needs into scalable solutions and supporting the adoption of emerging technologies across the organization. Key Responsibilities Support business teams in identifying opportunities to leverage AI and automation Gather, analyze, and document business requirements and translate them into functional specifications Act as a bridge between business stakeholders and technical implementation teams Promote and advocate for the use of AI and automation across the organization Assess and prioritize AI and automation use cases based on business value Coordinate and support the implementation of technology solutions in cross-functional projects Contribute to project delivery, ensuring alignment with business objectives Provide guidance, training, and support to users to ensure effective adoption of tools Analyze complex operational processes and propose improvements using digital solutions

Required Profile Minimum 8–10 years of experience as a Business Analyst, Project Analyst, or similar role Strong experience working on AI, automation, or digital transformation initiatives Solid understanding of project management principles and methodologies Strong analytical and conceptual thinking skills Proven ability to translate business needs into structured solutions Experience working in complex, cross-functional environments Ability to work independently, take initiative, and drive results Strong communication and stakeholder management skills Customer-focused mindset with a solution-oriented approach Technical & Functional Expertise Good understanding of AI technologies (e.g., machine learning, NLP, automation tools) Experience evaluating and implementing AI or automation use cases Familiarity with process optimization and digital transformation initiatives Knowledge of system integration and data-driven environments is a plus Education & Background Master’s degree in Engineering, Business, Science, or a related field (or equivalent experience) Key Competencies Excellent analytical and problem-solving skills Strong interpersonal and communication skills Ability to influence and engage stakeholders Adaptability in a rapidly evolving technological environment Team-oriented mindset with a proactive attitude Nice-to-Have Experience in regulated or complex operational environments Background in large-scale transformation programs Exposure to advanced data analytics or emerging technologies
Location : Belgium

2026-34882 - Cleaning validation engineer - Life Sciences - M/F/X

Tue, 23 Jun 2026 22:05:15 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As Cleaning Validation Engineer, you will join the Manufacturing Science and Technology (MSAT) team for one of our clients. This role focuses on cleaning validation processes within the manufacturing environment. You possess strong expertise in cleaning validation and API manufacturing processes, ensuring compliance with regulatory requirements. Besides this, you will manage the preparation and updating of cleaning validation documentation, support audits, and facilitate the introduction of new products and equipment into the validation program. This position requires a proactive approach to managing complexity and prioritizing tasks effectively. Key responsibilities Prepare and update cleaning validation documentation, including protocols, reports, and studies Prioritize and manage cleaning validation projects based on proposed changes Support audits and ensure compliance with regulatory requirements Facilitate the timely introduction of new products and equipment into the validation program Report incidents, deviations, and propose solutions to improve compliance with cGMP standards

About you Strong expertise in API manufacturing processes and cleaning validation Proficiency in project management, organizing, planning, and coordination Knowledge of statistics and data analysis tools Excellent communication skills and a result-driven personality Fluency in Dutch and English
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34881 - Project Engineer clean utilities - Life Sciences - M/F/X

Tue, 23 Jun 2026 22:05:15 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As a Project Engineer specializing in clean utilities, your role involves overseeing the engineering of clean utilities projects, ensuring compliance with industry standards, and coordinating with internal stakeholders. The position requires a strong background in engineering and project management. You will be responsible for the conceptual, basic, and detailed engineering phases, focusing on safety and quality throughout project implementation. Key responsibilities Develop and implement engineering plans for clean utilities projects in the pharmaceutical sector Coordinate and supervise the installation of equipment and piping systems Conduct verification and validation tests to ensure project compliance with safety standards Manage the purchase, start-up, and verification of installations Align specific utility planning with global project or operational timelines

About you Master's degree in civil, industrial, or bio-engineering, or equivalent experience in a scientific field Proven experience in clean utilities within the pharmaceutical industry Familiarity with formulation and preparation processes, including validation experience Strong project management skills with a focus on safety and quality Fluency in both Dutch and English
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34880 - Project Engineer Building - Life Sciences - M/F/X

Tue, 23 Jun 2026 22:05:15 Z

Category : OPERATIONS/CONSULTING
Contract : Fixed term contract
Position description :
About the role This role involves planning, coordinating, and executing technical projects with a focus on building automation and electrical systems. The Project Engineer Building will work closely with various teams and stakeholders to achieve project objectives within defined timelines and budgets. Responsibilities include overseeing technical aspects, preparing and implementing technical specifications, designs, and documentation, and providing technical support. The role requires effective communication and problem-solving skills to ensure project success Key responsibilities Follow up on capital projects in accordance with the CPMP methodology, focusing on civil constructions Supervise the construction of buildings and structures, including concrete floors and interior finishes Prepare technical specifications and compare bills of quantities for project execution Develop and manage project plans, including objectives, milestones, tasks, and resources Monitor project progress and identify and resolve any technical issues promptly

About you Minimum 3 to 5 years of experience as a Project Engineer in the construction industry Industrial Engineer or Civil Engineer with specialization in Construction Engineering Strong technical knowledge of civil structures and construction applications Native Dutch speaker with a good command of English for effective communication Ability to correctly interpret and review construction drawings on-site
Location : Noordkustlaan 16B 1702 Dilbeek

2024-31059 - Construction Manager - (Life Sciences) - F/M/X

Tue, 23 Jun 2026 22:05:05 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
Description du role de Construction Manager Pour un de nos clients,actif dans le secteur pharmaceutique, nous recherchons activement un Construction Manager Senior. Le Construction Manager est responsable de la gestion quotidienne ainsi que le suivi des chantiers de construction et de démolition. Il apporte son expertise en matière de construction afin d'assurer de la bonne exécution des différents chantiers. Il a un rôle d'expert technique lors de la phase d'études des projets de construction et assurera le suivi de chantier lors de l'exécution du projet. Il supervise les chantiers et s'assure que les normes de sécurité sont respectées. Vos responsabilités : Assumer la responsabilité générale du suivi et de l'organisation des activités de construction et de démolition liées au projet. Veiller à la préparation et à la mise à jour d'un plan de construction et de démolition complet qui coordonne toutes les activités de construction et de démolition du projet Fournir des ressources de gestion, le cas échéant, tout au long des phases de construction et de démolition afin d'assurer la coordination des activités et le respect des étapes convenues. Veiller à ce que les concepteurs, les entrepreneurs et les autres membres de l'équipe soient compétents en matière d'ESS et dûment préqualifiés. Veiller à ce que le directeur de la construction (entrepreneurs) réalise le projet en toute sécurité, conformément aux réglementations locales et aux exigences de l'entreprise. Convenir des responsabilités et des obligations de rendre compte en matière d'ESS pour la construction du projet avec le responsable ESS du site d'accueil. Encourager et soutenir une culture ESS conforme aux valeurs de l'entreprise. Rédiger le plan initial de sécurité de la construction (PSC) pour informer le directeur de la construction (entrepreneurs). S'assurer que tous les travailleurs reçoivent une initiation à la construction spécifique au site d'accueil et au projet Veiller à ce que le plan de sécurité de la construction soit régulièrement revu et mis à jour par le directeur de la construction. Mettre en œuvre un processus d'assurance des performances en matière d'ESS par le biais d'un programme d'audits, d'observations et d'interactions. Veiller à ce que le directeur de la construction (entrepreneurs) mette en œuvre un programme ESS proactif encourageant la reconnaissance.

Votre profil : Vous possédez un master Ingénieur civil ou industriel (construction, EHS, ,...) . Vous avez une expérience en gestion de projet (Capex et non Capex) ainsi qu’un bagage technique antérieur (construction, HVAC, facility, utilities, clean et black piping, EHS...) Vous avez une expérience en gestion de chantier de constructiondans l'industrie pharmaceutique, chimique, nucléaire, agro-alimentaire... Vous êtes capable d'établir et de maintenir un véritable partenariat au sein des équipes et des différents départements Vous êtes capable de gérer les différents stakeholders lié au projet Vous avez d'excellente capacité d'adaptation à un public (des ouvriers aux cadres supérieurs). Vous avez d'excellentes compétences en coordination du changement (change control) Vous parlez couramment français et anglais Contact infos : N'hésite pas à partager ton cv par message privé ou à m'envoyer un e-mail sur anissa.yahia-cherif@akkodis.com
Location : Avenue Jules Bordet 168 1140 Bruxelles
Language / Level :
French : 4 : Native / Bilingual level
Language / Level :
English : 3 : Advanced