RSS-Feeds der Stellenangebote - Nur Top-Jobs : Nein / Land : Europe-->Belgique, Europe-->Royaume-Uni / Standort : Europe-->Belgique-->Flandres-->Flandre orientale

2017-1939 - Project Engineer M/F - Secteur Pharmaceutique

Wed, 27 May 2026 22:03:10 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
QUI SOMMES NOUS ? Akkodis Belgium, filiale Belge du Groupe Akkodis, est aujourd’hui n°1 sur le marché belge du conseil en ingénierie industrielle et compte plus de 1000 experts. La société accompagne depuis près de 30 ans les plus grands industriels du pays sur les différentes étapes de leur projet à forte valeur ajoutée, dans les secteurs novateurs – aéronautique, spatial, ferroviaire, automobile, sciences de la vie, énergie, high-tech - en œuvrant à la construction du monde de demain. VOS RESPONSABILITIES : En tant que Project Engineer, vous êtes en charge du planning, de la gestion et la coordination du travail des différents acteurs (internes & externes) sur site pharmaceutique. Vous contribuez à la définition du projet, suivez son implémentation et êtes force de proposition ; Vous établissez et êtes garant du planning ; Vous rédigez les protocoles & rapports de validation, ainsi que d’autres documents nécessaires ; Vous garantissez la coordination du travail des différentes équipes concernées par votre projet, ainsi qu’une excellente communication entre elles.

VOTRE PROFIL : Vous possédez un master Ingénieur civil ou industriel (biologie, chimie,...) ou un titre de pharmacien industriel. Vous avez une première expérience solide de Projet Engineer au sein d’un environnement pharmaceutique (connaissances GMPs, réglementation FDA...). Vous parlez couramment français et anglais. Vous avez déjà travaillé au sein d’équipes pluridisciplinaires. Vous êtes autonome, dynamique, curieux et flexible. NOTRE OFFRE : En tant que consultant Akkodis, vous serez: En charge de divers projets tranverses et responsabilisants Accompagné dans votre carrière par votre Manager Akkodis Acteur de votre plan de formation et de votre développement personnel et professionnel Membre d’une communauté d’ingénieurs dynamique et collaborative Bénéficiez d’un contrat permanent Ainsi que d’un package salarial attractif incluant plusieurs avantages extra-légaux
Mindestanforderungen Ausbildungsniveau : 7. Meister

2021-17037 - Ingénieur Sûreté de Fonctionnement/RAMS F/H

Mon, 25 May 2026 22:04:27 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Dans le cadre du développement de nos activités dans le secteur de la mobilité, nous sommes à la recherche d'un ingénieur RAMS/ sûreté de fonctionnement. Responsabilités: Analyse des Modes de Défaillance, de leurs Effets et de leur Criticité (AMDEC) du système considéré Présentation des modes de fonctionnement (nominale / dégradée) du système considéré Analyse de fiabilité du système considéré Représentation graphique du système sous forme de Blocs Diagrammes de Fiabilité (BDF) Réalisation de la modélisation des BDF sous le logiciel SIMFIA et la quantification des différents paramètres FMD tels que : Evaluation du taux de disponibilité intrinsèque à la mer du système incluant des préconisations de passage d’un article non réparable à réparable en mission Evaluation du Mean Time Between Failure (MTBF) et du Mean Time Between Critical Failure (MTBCF) du système Analyse de maintenabilité comprenant :Sélection des équipements réparables en mission et pour chaque équipement réparable retenu. Attribution d’un Mean Time To Repair (MTTR) exprimé en heures. Evaluation du MTTR pour chaque système.

Votre profil: Ingénieur industriel spécialisé en sûreté de fonctionnement et/ou gestion de risques industriels 6 mois à 2 ans d’expérience (stages et alternance valorisée) en RAMS/Sûreté de fonctionnement dans l’industrie Une 1ère expérience en FMDT (fiabilité, maintenance, disponiblité, testabilité) dans le domaine du Naval est un plus Vous maitrisez un logiciel de simulation RAMS (ex : Simfia) Vous parlez couramment Français et Anglais Vous pouvez être disponible mi-avril au plus tard pour le démarrage du projet Vous êtes en possession d’un passeport européen (requis pour pouvoir travailler sur le projet)
Standort : Bruxelles
Mindestanforderungen Ausbildungsniveau : 6. Master / Diplom
Sprache / Abschluss :
französisch : 3: Fortgeschrittene Kenntnisse
Sprache / Abschluss :
englisch : 3: Fortgeschrittene Kenntnisse

2023-26429 - Ingénieur/ Spécialiste Supply Chain - Aéronautique

Sun, 24 May 2026 22:05:04 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : V.I.E
Beschreibung der Stelle :
Rapportant au Leader Approvisionnement, votre mission est d assurer l approvisionnement en pièces et matières premières, en optimisant les coûts et les paramètres logistiques. Vous devrez prendre en charge la gestion (l'expertise) Supply Chain au sein d une ou plusieurs commodités, avec un esprit fort de leadership et de réussite des objectifs internes. En relation essentiellement avec les services achats, qualité, production, logistique, ordonnancement, commercial et comptabilité, vous devez donc, au sein de l équipe multi-métiers de la commodité : - Négocier et sélectionner les fournisseurs ; - Gérer les approvisionnements série et sous contrat de la commodité ; - Suivre et optimiser les stocks; - Fiabiliser, optimiser les paramètres et les besoins ; - Gérer la performance logistique des fournisseurs ; - Mesurer, suivre et améliorer les performances Délais et Coûts logistiques en commodité ; - Mener des projets d amélioration continue en Supply Chain ou transverse.

- Master en Supply Chain - Expérience en supply chain, approvisionnement ou planification en général (ordonnancement, gestion de production, etc.) dans l'industrie - Vous êtes disponible pour des déplacements (Europe, USA, Brésil, ) - Vous maîtrisez les outils informatiques Suite office (avec EXCEL confirmé, ) - Vous avez une bonne connaissance du fonctionnement MRP - SAP - Vous parlez très bien l'anglais (Anglais courant). Ce poste est ouvert pour des profils en début de carrière, accessible aussi via un contrat CDI qu'un VIE.
Standort : Avenue Jules Bordet 168 1140 Bruxelles
Mindestanforderungen Ausbildungsniveau : 6. Master / Diplom
Sprache / Abschluss :
französisch : 4: Muttersprachliches Niveau
Sprache / Abschluss :
englisch : 3: Fortgeschrittene Kenntnisse

2023-29473 - Launch Support Engineer

Wed, 06 May 2026 22:05:25 Z

Berufsprofil : OPERATIONS/Consulting
Vertragsart : Festanstellung
Beschreibung der Stelle :
Job Title: Launch Support Engineer Location: Crewe, United Kingdom (Onsite) Responsibilities: Support is required to cover the production phases of all customer vehicles, the load rate for these is approximately 1 per month. Professional services to achieve the below deliverables. Provide progress/status reports in line with project timings Creation and maintenance of Daily build plans, respecting the high-level customer delivery plan. To Liaise and interface with all elements of the project delivery team to support the build of the Customer vehicles, these areas including, project management, Operations, Workshop, and Various Engineering departments, - (This list is not exhaustive) Build documentation into relevant Bentleys systems to provide traceability of the build process of the vehicles, inclusive of History books and Control plans Agreeing on the build process for all affected componentry with all stakeholders internally and externally Ensuring that build feasibility is agreed with respect to the above Build-related problem resolution where required when vehicles are in assembly Provide progress/status reports in line with project timings using standard client formats where applicable Experience BiW, Body Sealing, Exterior/Body Hardware and Dynamic Sealing Systems, Teamcenter PLM Build Support experience Applicable legislation and certification requirements Engineering degree or equivalent qualification

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Standort : Crewe CW1

2026-34883 - Data Engineer

Tue, 27 Jan 2026 12:36:56 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Akkodis is seeking a skilled Data Engineer to join its innovative and technology-driven teams. The Data Engineer plays a key role in designing, building, and maintaining scalable and reliable data platforms that enable data-driven decision-making across business, R&D, and digital products. The position focuses on data ingestion, transformation, storage, and secure access to data within modern cloud-based architectures, working closely with stakeholders, architects, analysts, and developers. Role : Understand business, R&D, and technical requirements related to data usage Design, build, and maintain robust and scalable data pipelines (batch and streaming) Extract raw data from multiple sources such as APIs, databases, files, IoT systems, and third-party platforms Transform, clean, enrich, and standardize data according to a centralized data model Develop and maintain backend services and REST APIs to expose data to web applications, BI tools, and analytics platforms Manage data storage within data lake, lakehouse, and data warehouse architectures Implement access control, security, and data governance policies across the data platform Ensure data quality, reliability, observability, and performance of data pipelines Optimize SQL queries and data processing workloads Support reporting, dashboards, and advanced analytics use cases Collaborate with data scientists, analysts, architects, product owners, and project managers Contribute to data engineering standards, best practices, and architectural guidelines Support end-to-end delivery from requirement analysis to production deployment

Your profile : Bachelor’s or Master’s degree in Computer Science, Data Engineering, or related field Minimum 3 years of experience as a Data Engineer (medior/senior profiles preferred) Experience in R&D, innovation, or technology-driven environments is a plus Strong proficiency in English (written and spoken) Knowledge of French and/or Dutch is an asset Strong interest in modern data technologies and continuous improvement Data Engineering and data pipeline development (ETL / ELT) Strong SQL skills and experience with relational and analytical databases Programming languages: Python (mandatory), knowledge of Scala or Java is a plus Big Data and processing frameworks: Spark, Databricks or equivalent Workflow orchestration tools: Airflow, Azure Data Factory, or similar Cloud platforms: Azure (preferred), AWS or GCP Data storage architectures: Data Lake, Lakehouse, Data Warehouse REST API development and integration Containerization and deployment: Docker, Kubernetes BI and visualization tools: Power BI, Tableau or similar Understanding of data modeling, data governance, and security principles
Standort : Belgium

2026-34885 - Data Analyst

Tue, 27 Jan 2026 12:35:15 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Akkodis is seeking a talented Data Analyst to support one of its clients in delivering high-quality data analysis and reporting solutions. The Data Analyst plays a key role in transforming business data into meaningful insights by designing, developing, and maintaining dashboards and reports. The position involves close collaboration with business users, key stakeholders, and IT teams to ensure data accuracy, consistency, and alignment with business processes, particularly in ERP-driven and industrial environments. Role : Analyze, qualify, and prioritize reporting and analytics requests submitted by business users through a ticketing system Design, develop, and test new reports and dashboards using BI tools such as Qlik Sense and Power Query Adapt, optimize, and maintain existing reports according to evolving business needs Validate reports by ensuring data accuracy and consistency with business processes and ERP systems Integrate and analyze data from ERP systems (e.g. SAP) and other source systems Define and document detailed functional and technical specifications for each reporting request Document delivered reports to ensure proper understanding and usage by end users Provide training and functional support to business Key Users, including guidance on report usage and documentation Evaluate and validate proposed ERP process improvements, analyzing data impacts and overall consistency Communicate regularly with business stakeholders on report evolutions, changes, and delivery status Propose and implement corrective actions in collaboration with business referents

Your profile : Data analysis and business intelligence fundamentals Strong experience with BI and reporting tools: Qlik Sense, Power Query Solid SQL knowledge (MySQL or equivalent) Good understanding of relational databases and data structures Experience with ERP systems (SAP knowledge is a strong asset) Data validation, reconciliation, and quality control Basic proficiency with Microsoft Office (Excel, PowerPoint, Word) Understanding of business processes, preferably in industrial environments Strong proficiency in English and French (written and spoken) Experience in an industrial or manufacturing environment is a plus Ability to interact with Key Users and business stakeholders Familiarity with ticketing tools and structured request management Strong attention to data accuracy and consistency
Standort : Belgium

2023-26479 - QC Analyst

Mon, 28 Apr 2025 08:29:25 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. Major Responsibilities: Responsible for the completion of QC testing related to the manufacturing of autologous products for clinical trials and commercial operation in a controlled cGMP cleanroom environment. Ensure testing is completed in compliance with all applicable procedures, standards and GMP regulations. Work with Process Development team, Quality and Operations organization to successfully transfer process/analytical testing to cGMP facility to manufacture products. Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories. Perform peer review/approval of laboratory data. Utilize electronic systems (LIMS) for execution and documentation of testing. Create, review and approve relevant QC documents, SOP’s and WI’s. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Other duties will be assigned, as necessary

Education: A minimum of a Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required or relevant years of experience within the pharmaceutical industry. Experience: A minimum of 1-2 years relevant work experience is required. It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy. Capabilities, Knowledge, and skills: Experience in a Quality Control setting is preferred. Experience with aseptic processing in ISO 5 clean room and biosafety cabinets is required. Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products is required. Knowledge of Good Tissue Practices is required. Detailed knowledge of QC test methods and related equipment is preferred Excellent written and oral communication skill are required Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process. Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice. The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision. Comfortable with speaking and interacting with inspectors. This position may require occasional travel to partner sites in NJ or PA as business demands. This position may require up to 10% domestic or international travel as business demands. Language(s): English
Standort : Brugge

2023-26478 - QA Investigator

Mon, 28 Apr 2025 08:29:04 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Role Overview: The QA Investigator is an exempt level position with responsibilities for providing quality oversight over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment. This includes supporting and approving manufacturing investigations, ownership of various department projects, and tracking of quality metrics while ensuring high quality and compliant product supply. Major Responsibilities: Collaborate with site personnel to provide guidance and determine resolution for manufacturing issues. Ensure accurate and timely maintenance and review of manufacturing investigations, CAPAs, change controls and complaints. Perform analysis on quality indicating data and identifying trends. Collaborates with functional departments to resolve issues. Manage cross-functional projects with many stakeholders. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Require minimal direction to complete tasks, knows how to get resources and information from established internal contacts; consult with manager for decisions outside established processes. Provide guidance to other employees in the interpretation of quality issues and participate in the development of technical or scientific initiatives and activities. Routinely recognize and resolve quality issues. Seek management guidance on complex issues. Drive continuous improvement.

Education: A minimum of a Bachelor’s Degree in Science, Information Science or equivalent technical discipline is required. Experience: A minimum of 4 years relevant work experience is required. It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy. Key Capabilities, Knowledge, and Skills: Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices. Strong interpersonal and written/oral communication skills. Ability to quickly process complex information and often make critical decisions with limited information. Proficient in applying process excellence tools and methodologies. Ability to pay attention to details and follow the procedures. The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision. Good written and verbal communication skills are required. Ability to summarize and present results, and experience with team-based collaborations is a requirement. Ability to work with others in a team environment. Detailed knowledge and understanding of current Good Manufacturing Practices (cGMP) and current Good Tissue Practices (cGTP) related to CAR-T manufacturing or cell processing. Ability to identify/remediate gaps in processes or systems. Experience with ICH and/or 21 CFR parts 210, 211, 1271 is required and 600, 601, and 610 is preferred. Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint). Language Requirements: Dutch and technical English
Standort : Ghent

2023-26477 - Software Test Design engineer

Mon, 28 Apr 2025 08:28:46 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Product quality and Customer satisfaction are the main targets. Design software verification test for H&F software components, through Hardware In the Loop, Virtual Verification and Digital Twin, including test cases description and human machine interface. Guarantee no safety issues and serious malfunctions due to software bugs or lack of system integration are present at the end of validation process, in accordance with system specifications, Functional Software specification, diagnosis specification, Interlock specification and Functional Safety documentation. Secure correct deployment of Test Environment configurations and processes. With attention to Test Environment:secure on time availability of testware suites meant to check multiple Electronic Control Unit functionalities and their integration. Guarantee correct Test Environment setup for HIL, VV and DTwin Guarantee correct software issues description and collection through Data Management tool. Design all maneuvers meant to support module SW verification AND testware development. Essential responsibilities: Develop the automatic testcase as per Test Plan from the system and vehicle specifications, defining the integration test and the validation test protocol. Automatic testcase it’s an important asset of Design Verification team. Guarantee the execution of the test activity according to the Test Plan and sw Validation timeline for the release to production in agreement with Stakeholder. Guarantee correctness of HIL/VV/DTwin configurations.

Qualifications/requirements: Electric/Electronic Engineering Master’s degree or equivalent. Basic knowledge of virtual test environment for SW validation (skill on tools as dSPACE is a plus) with passion on test automation. Knowledge of Matlab/Simulink/State Flow Knowledge of Python programming language. Knowledge on Vector tools, likes CANalyzer, for CAN BUS protocol or LIN. Knowledge of electronic tools/devices and schematics. Knowledge of the issues relating to interfacing of sensors/actuators with electronic control units Skills to work on more projects in parallel. Brief experience in Automotive field. Be curious, proactive, supportive, and willing to learn. Preferred : From 1 to 3 years of experience as SW Test Engineer is preferred. Knowledge on hydraulic control devices used on agricultural systems and related control designs characteristics Languages: English (Dutch is a plus)
Standort : Brugge

2023-26476 - Embedded Software Designer

Mon, 28 Apr 2025 08:27:57 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Convert system requirements into embedded vehicle software Design the system control strategy and corresponding software architecture Maintain, archive, and control application source code. Manage SW releases. Implement the software architecture and strategies, requirements for closed loop control algorithms, and related software control logic in C or MATLAB/Simulink Define & Execute test scenarios to verify the implemented control / monitoring strategy. Verify the implementation in a virtual simulation environment Create tools/applications to test your code more efficiently and automatically Verify the implementation on the physical vehicle Support Product Validation Engineers as they conduct Functional and Performance testing. Produce documentation in support of design, implementation, and test activities.

Master in Electronics/ICT or equivalent by experience Experience in C-programming Knowledge of MATLAB/Simulink is a plus Affiliation with agricultural machinery and hands-on mentality Team player with good communication skills Knowledge on SAE J1939, CAN, UDS and ISOBUS software protocols is a plus
Standort : Brugge

2023-26474 - Production Planning & Control Process Advisor

Mon, 28 Apr 2025 08:27:37 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Guide plants for MOP (methods of procedure) development, lead the Industrial portion of the S&OP process, validate changes on the Commercial Requirements, assess impact on MFG Plants, find best possible solution to satisfy the requirements (Calendar, Daily rate, Off line, OKTS, and Fleet management) in the MFG Operating Plan, including Component Plant impacts. Document cost impact (down days, overtime, rebalances, HC termination, ....) Manpower consolidation after MOP cycle Lead Industrial portion of the Sales and Operations planning (S&OP) process, respecting WW S&OP timeline Component Plant Requirements, based on Final Plant MOPs, manage constraints, solve capacity issue between final plants and component plants Manage the "Material Overplanning" process in the plants, both Final Assy Plants as well as Component Plants, thru MRP MOPs, in order to book capacity in the supply base Ensure Off Line / OKTS in line with Plan, OKTD to support the Wholesale plan of Commercial, manage the Blocked Units / FAI OK on PAD delay Ensure the Order Coherence process monitoring (working with Plant, S&OP and Commercial) Priority setting to support specific commercial priorities Launches in line with Platform Plan (Check alignment the to product Launches plan)Team work with SharePlan Team and SupplyChain KPI team for Mop tools improvement and process improvement

Daily interaction with Plant, Procurement and Purchasing/Commodity (plants antennas,…) to highlight potential gaps and ask for support where not possible to achieve on our own. Weekly attendance to the L2/L3 call. Within L2, support and follow up to suppliers as requested. Guide arbitration between plants and region. Support to the Interplant planning process for components Standardized Plants view of requirements data to allow to drive suppliers through arbitration. Std management document showing status / progress, allowing to take the decision to remove supplier from crisis follow-up (back to normal process) Interaction with suppliers to delivery in line with the given promises and share new promises. Ensure plants achieve expected delivery Performance to Spare Parts on FLT's, and maximize the performance on SLT and Urgent orders to minimize the impact for our final customers Support to the Plant to analyze the root causes in order to eliminate/reduce the Urgent Freight WMF NA flow providing weekly analysis of the promises of the suppliers highlighting points of attentions (missing promises, past dues, blocked orders etc.). Weekly analysis of the aging inventory at ISC. Assure plants meet Inventory Levels targets: Manage BDG & Fcst1/2/3 Inventory target planning, in coordination with Finance.
Standort : Brugge

2023-26472 - Precision Technology Program Manager

Mon, 28 Apr 2025 08:25:00 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
In Precision Technology, we make iron smarter. Our team members deliver innovative solutions helping our customers to be more productive, save time, lower costs, and to operate sustainably. From vehicle displays, application controls, steering solutions, digital services and telematics, to fully autonomous driverless technology, we develop solutions that solve challenges for customers around the world. As the Precision Technology Program Manager with Equipment Portfolio team, you will be responsible to plan, manage, and direct all product development activities, to meet customer needs and fit within the capabilities of the Precision Technology team. The Equipment Portfolio team works across component and platform programs to ensure that on time launch of products to meet the customer needs, thereby having a positive impact on the business. Manage end to end execution of Precision Technology deliverables for major equipment programs Manage end to end execution of Precision Technology initiatives/projects. Work closely with internal and external teams (Product Marketing Mangers, Technical Product Managers, Engineering/Development, Architecture, Security, Product Validation, etc.) to develop and execute short-term and long-term plans, policies, procedures, resources, and initiatives. Work with leadership team to maintain accountability to budgets, plans, and initiatives. Gains knowledge of the customer and business needs; thereby contributing to strategic decisions. Measure and monitor project performance. Create and review project status reports to support close surveillance over product development and support events to assure proper allocation of resources. Ensure project plans and timelines are met by internal and external resources through Program Increment (PI) team plans and commitments. Understand and manage the program risk throughout the life cycle. Serve as a liaison and mentor to assist with and expedite product related issues. Assist with contract review and meeting the requirements. Monitor and initiate improvement projects to current processes or policies. Holds post-program lessons learned to look for issues and opportunities for improvement. Effectively communicate to stakeholders with the appropriate content and frequency. Provide feedback to the PMO regarding process items that could improve the efficiency and effectiveness of the entire product development process.

Bachelor’s degree in Engineering, business, or related technical field Minimum of 4 years of experience in software/electronic hardware; or equivalent combination of education and experience Thorough knowledge of product development and procedures, including general finance exposure Ability to manage a diverse range of technical operations Experience managing budgets and increasing efficiencies Knowledge of Agile frameworks such as Scrum, SAFe, Kaizen PMP or Six Sigma preferred Demonstrated leadership, organizational, documentation, analytical, and decision-making skills Strong skills in the Microsoft Office Suite (Outlook, Excel, Project)
Standort : Brugge

2023-26480 - QC Investigation Specialist

Mon, 28 Apr 2025 08:24:39 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Role Overview The QC Investigation Specialist is an exempt level position with responsibilities for leading deviations and corrective actions in support of the QC testing laboratories related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. Major Responsibilities: In this function you will be responsible to manage the QC related deviations and execute qualitative investigations in close collaboration with the analysts and the involved stakeholders according to the required procedures. Ensuring thorough root cause analysis is performed using the correct tools and proper CAPAs are defined in order to reduce non-conformances and deviations in the future. Different tasks are (but are not excluded to) Review/complete routine manufacturing and QC nonconformance/deviation investigations. Interview personnel within QC and provide quality insight to complete laboratory investigation reports in Trackwise. Proactively work with stakeholders to implement effective CAPAs and to ensure the timely completion of corrective and preventive actions within the laboratories. Provide recommendations for the improvement of processes by working cross functionally with multiple stakeholders. Work closely with management to propose/execute improvements through the change management system. Drive continuous improvement. Ability to respond with a high degree of urgency to departmental and cross functional needs and requests. Reporting/Monitoring metrics on non-conformance investigations and corrective and preventive actions (CAPA). Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Comply with all training requirements to perform duties on the job.

Education: A minimum of a Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required and relevant years of experience within the pharmaceutical industry. Experience: A minimum of 4 years relevant work experience is required. It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality control, quality assurance, manufacturing compliance, clinical quality, or cell therapy. Capabilities, Knowledge, and skills: Experience in a Quality Control setting is preferred. Experience with aseptic processing in ISO 5 clean room and biosafety cabinets is required. Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products is required. Knowledge of Good Tissue Practices is required. Detailed knowledge of CAR-T QC test methods and related equipment is preferred. Excellent written and oral communication skill are required. Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process. Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice. The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision. Comfortable with speaking and interacting with inspectors. Language(s): Dutch & English
Standort : Ghent

2023-26496 - QC Manager

Mon, 28 Apr 2025 08:24:20 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Role Overview The Associate Manager/Manager, Quality Control is an exempt level position with responsibilities for managing the operation and worklflow of the quality control laboratories in support of cell therapy manufacturing. This includes hiring, development and performance management of staff, reviewing/approving laboratory test data, procedures and methods, supporting laboratory investigations and ownership of various QC microbiology department projects. Major Responsibilities: Ensuring adequate training (skills-based, cGMP and safety) of associates within the department. Raw material, in-process, environmental/utility, product release, and stability testing. Investigation of laboratory non-conformances (events, deviations, and invalid assays). Maintenance, calibration and qualification of laboratory instruments and equipment. Test method verification, qualification, validation and/or transfer activities in the QC laboratories. Process Performance Qualification and Continued Process Verification activities associated with QC microbiology laboratory testing. Providing expertise in troubleshooting complex laboratory issues and demonstrating strong reasoning skills in support of ongoing laboratory investigations. Maintain detailed knowledge of industry guidelines/trends, regulatory requirements, and applicable pharmacopeia while remaining current in on the-job training requirements. Collaborate with Quality Assurance, Manufacturing, Technical Operations, Engineering and Maintenance to support business needs. Contribute to global strategies related to QC laboratories which align with compliance and business objectives as well as the overall corporate vision. Manage departmental budget and resources; prepare staffing plans. Make adjustments to roles and responsibilities of department to meet business needs. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Other duties will be assigned, as necessary

Education: A minimum of a Bachelor’s Degree in Science, Information Science or equivalent technical discipline is required. Experience: A minimum of 8 to 10 years relevant work experience is required. It is preferable that the candidate has experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy. A minimum of 1 to 4 years of leadership experience is also required. Capabilities, Knowledge, and skills: Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices. Strong interpersonal and written/oral communication skills. Proven people management and leadership experience is required. Experience working with quality systems is required. Extensive knowledge of chemical, biochemical and microbiological concepts is required. Experience with aseptic processing in ISO 5 clean room and biosafety cabinets is preferred. Ability to quickly process complex information and often make critical decisions with limited information. Ability to handle multiple priorities on a daily basis while being flexible and responsive to frequently shifting priorities. Proficient in applying process excellence tools and methodologies. The candidate must be highly organized and capable of working in a team environment with a positive attitude. Good written and verbal communication skills are required. Ability to summarize and present results, and experience with team-based collaborations is a requirement. Experience developing and setting long-term objectives. Ability to identify/remediate gaps in processes or systems Experience with ICH and/or 21 CFR parts 210, 211, 1271 is required and 600, 601, and 610 is preferred. Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint). This position may require up to 10% domestic or international travel as business demands Language(s): Dutch
Standort : Ghent

2023-26503 - Quality Person In Plant

Mon, 28 Apr 2025 08:24:03 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Role Overview: The Quality person in plant is an exempt level position with responsibilities for providing quality oversight over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment. Job duties are performed within a team according to an assigned, production shift schedule. This role will work in shift regimes supporting the 7/7 days cell processing. Major Responsibilities: Serves as a Quality person in plant in support of cell therapy manufacturing. Ensures Quality Oversight in plant covering various process related activities Performs periodic Quality checks/audits related to process, documentation and process manipulations Strive to reduce non-conformances and deviations in supported areas by proactively driving compliance. Responsible for real time review of process documentation in support of process unit operations and release activities where needed. Collaborate with site personnel to provide guidance and determine resolution for manufacturing issues. Supports in accurate and timely input, investigation and review of manufacturing deviations, CAPAs, change controls and complaints. Review and approve manufacturing procedures and batch records Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Support regulatory inspections and audits by ensuring inspection readiness within facility. Perform internal housekeeping audits. Other duties will be assigned, as necessary.

Education: A minimum of a Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required or relevant years of experience within the pharmaceutical industry. Experience: A minimum of 2 years relevant work experience is required. It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy. A minimum of 2 years of experience with quality support in clinical manufacture is preferred. Key Capabilities, Knowledge, and Skills: Aseptic processing in ISO 5 clean room and biosafety cabinets. Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products as well as knowledge of Good Tissue Practices. Great attention to detail and ability to follow the procedures. The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision. Good written and verbal communication skills are required. Ability to summarize and present results, and experience with team-based collaborations is a must. Must be able to interpret problems and effectively determine appropriate resolutions that ensure compliance and minimize risk. Must exhibit strong leadership skills and effectively develop others. Ability to collaborate well with stakeholders, customers and peers. Must exhibit strong decision-making ability and think creatively while maintaining compliance and quality. Must be able to discern the criticality of issues and to communicate to management regarding complex issues. Ability to manage conflict and issues that arise with internal or external customers. Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process. Language Requirements: Dutch and technical English
Standort : Ghent

2023-26467 - Continuous Improvement Project Engineer

Mon, 28 Apr 2025 08:23:28 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Facilitate Kaizen Events in which a cross-functional team works in a focused manner to implement their improvement ideas. Assist the Operations team in their 'root cause problem solving' analyses (following from reporting the daily management gemba walk). Identify and reduce process waste.

Bachelor or Master's degree in electro-mechanics with at least 2 years' experience. Strong interpersonal and communication skills. An intrinsic motivation to improve processes. Capable of coaching and leading cross-functional team within a given scope. Strong analytical skills. Creative in problem solving. Microsoft Office skills such as PowerPoint, Excel and Word. Hands on mentality. Competent to quickly learn (complex) manufacturing processes and collaborate with others to identify opportunities data driven. Competent to teach and coach colleagues new knowledge in Continuous Improvement concepts. An initial Maintenance / Manufacturing / Engineering / QA / QS experience is a plus 2 years' experience in similar sector. Good knowledge of the Dutch language, both oral and written, is required.
Standort : Brugge

2023-26727 - Adjoint Administrateur ERP/BI

Mon, 28 Apr 2025 08:23:08 Z

Berufsprofil : SUPPORT/Einkauf
Vertragsart : Festanstellung
Beschreibung der Stelle :
Introduction Nous recherchons pour notre client situé à Libramont et Recogne un Adjoint Administrateur ERP/BI, prêt(e) à évoluer dans une équipe engagée et dynamique Mission Adjoint à l’administrateur ERP/BI au sein d’un environnement IT 4.0 / Industrie 4.0 agro-alimentaire, vous êtes l’un des moteurs de la transformation digitale et de la maturité informatique. Votre activité consiste à intégrer/paramétrer les outils de l’informatique de gestion. Vous partagez les tâches avec l’administrateur ERP autour des sujets ERP (Microsoft D365 F&O) mais aussi CRM (Microsoft CRM) et BI (Power BI) afin qu’ils permettent de piloter les processus métier. Vous êtes intégré à une équipe IT pluridisciplinaire se chargeant aussi bien de l’infrastructure que de l’ERP ou de développement applicatifs spécifiques. Vous êtes partie prenante sur les aspects architecturaux de ces solutions afin de garantir une forte intégration transverse. Tâches 1.1. Analyser et concevoir > Vous devez vous rapprocher des différents départements de l’entreprise afin de bien analyser leurs méthodes et besoins permettant de définir les configurations qui pourraient fluidifier leur travail en augmentant l’efficacité. > Vous participer aux ateliers de cadrage et de conception dans le cadre de la finalisation de la mise en place du nouvel ERP. > Conjointement avec le département de contrôle de gestion, vous collaborer par un apport conceptuel et technique à la mise en place de rapports analytiques construits avec Power BI > Conjointement avec le département commercial, vous collaborer par un apport conceptuel et technique à la mise en place du CRM. > Vous paramétrez et intégrez les différents outils d’édition de documents et les échanges EDI. 1.2. Mettre en place > Conjointement avec l’équipe IT et les prestataires applicatifs, vous co-pilotez, l’exécution des travaux nécessaires à la finalisation de mise en place de l’ERP. > Vous serez amenés à participer au paramétrage des systèmes ERP-CRM-BI-EDI. > Vous êtes le concepteur technique de la BI avec nos partenaires. Vous réalisez les rapports, organisez les sources de données (Dataware) et écrivez les codes DAX. > Vous alimentez nos développeurs et prestataires sur les besoins spécifiques et vous vous assurez de leur mise en œuvre. > Vous validez et structurez la documentation des systèmes installés. > Vous accompagnez de manière les key-users afin de les écoler sur les outils mis en place. 1.3. Contrôler > Conjointement avec l’administrateur ERP, vous réalisez les suivis de projets afin de garantir que les architectures décidées sont bien respectées et vous êtes capable de vous positionner en leader face aux intégrateurs. > Vous vous assurez de la performance des systèmes en place et vous organisez la mise sous monitoring. > Vous organisez la revue des processus. 1.4. Ajuster et opérer > Vous êtes l’un des administrateurs principaux

· Master ou bachelier en contrôle de gestion de préférence ou équivalence par expérience ou bachelier IT avec expérience en contrôle de gestion, reporting Power BI, compta/achat · La connaissance d’une solution ERP est souhaitée. · La connaissance de Microsoft D365 F&O est un plus (est un grand atout · La connaissance de Microsoft Power Bi est souhaitée. · Une expérience probante en langage ‘DAX’ est un plus. · Bonnes notions en base de données relationnelles (SQL server ou équivalent). · Une expérience dans la gestion de master data industrielles est un plus. · Maitrise des outils Microsoft Office conventionnels. · L'autonomie dans le travail et une capacité de décision. · De bonnes dispositions au travail d'équipe et gestion du changement : dialogue, échanges d'informations avec les autres métiers, pédagogie. · De bonnes capacités d'analyse et de résolution de problèmes. · De la rigueur journalière dans l'application et dans la documentation. Language · Français: excellente communication orale et écrite · Anglais : bonne communication (écrite et orale) Offre: Etes-vous ouvert pour un nouveau challenge dans une entreprise stable avec : · Un contrat à durée indéterminé (pas de mission de freelance) · Des projets intéressants qui boostent votre expérience et vos projets · Un chaleureux accueil · Un salaire attrayant accompagné d’avantage extra-légaux : · Un parcours d’intégration personnalisé pour vous accompagner dans votre prise de poste Contact Vous êtes intéressé par un nouveau défi? N’hésitez pas à contacter Sylvie au 0496/69 05 79 ou envoyer votre CV à sylvie.antoine@akkodis.com
Standort : Avenue Jules Bordet 168 1140 Bruxelles
Mindestanforderungen Ausbildungsniveau : 5. Bachelor
Sprache / Abschluss :
französisch : 4: Muttersprachliches Niveau
Sprache / Abschluss :
englisch : 3: Fortgeschrittene Kenntnisse

2023-26499 - QC Sample Coordinator

Mon, 28 Apr 2025 08:21:19 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
Role Overview The QC Sample Coordinator, is responsible for sample management. The QC Specialist is encouraged to work independently on routine tasks and have conceptual understanding of all Quality Control functions and business areas. May need supervision/support to resolve some sophisticated issues. He/ She will serve as technical specialist within job function. Thinks logically and acts decisively. Major Responsibilities Prepares and reviews documentation independently Responsible for QC sample and retain management Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) and lab management software system (LIMS) Prepare documents and coordinate Sample shipment (internal and external shipments) Review logbooks and/ or LIMs to align physical quantities of samples in freezers/refrigerators Periodic inspection and consolidation of retains Document and perform sample management related non-conformance investigations Document and handle corrective and preventative action records Supports internal and regulatory audits

Requirements A minimum of a Bachelor’s degree or higher A minimum of two (2) years related experience in medical device, biopharmaceutical, or pharmaceutical industry A degree in Biology, Biochemistry, Microbiology, Chemistry or related field Solid understanding of regulatory requirements, policies and guidelines Experience with Quality Control document reviews and regulatory inspection processes Working knowledge of Quality systems Experience in management of retain samples using electronic systems (eLIMS) Candidates must be able to accommodate shift schedule. Shifts include weekend and evening work as required by the manufacturing process This position will be located in Ghent and may require up to 5% of travel This position will occasionally require to lift up to 10 kg Language Requirements: Dutch and Technical English
Standort : Ghent

2023-29474 - Vehicle Electronics & Network Development Support

Thu, 02 Nov 2023 09:55:57 Z

Berufsprofil : OPERATIONS/Consulting
Vertragsart : Festanstellung
Beschreibung der Stelle :
Job Title: Vehicle Electronics & Network Support Location: Crewe, United Kingdom Department: Electrical Engineering Responsibilities: Working on the client Product Emergence Process to deliver to the required business expectations of the engineering department. Ensuring correct documentation and validation of the parts and functions ensuring engineering sign-off is achieved through testing and validation at differing integration Levels (BiL points)/vehicle build and development timing points which require specific validation events. Liaison within the E/E department to ensure delivery of the expected functionality. Working with group stakeholders directly and/or indirectly to understand functions/parts/systems and the client requirements. Organisation of test facilities and arrangements to test functions on vehicles. Requirements: Detailed knowledge of CAN/Ethernet communication protocol Detailed knowledge and experience of Electronic Control Unit development from concept to series parts. UDS diagnostic protocol and diagnostic understanding. Knowledge of off-board communication protocols and Automotive Network Access devices Integration of vehicle networks to determine failures with the network and/or routing Understanding or an appreciation of the vehicle connectivity unit connection to the backend/cloud systems and the communication protocols used within these systems. Experienced in the use of Vector CANoe Understands the concept of distributed functions throughout the vehicle in order to realise functionality. Understand the requirements for data logging of CAN/Ethernet networks and use of data to problem-solve network and network gateway issues. BOM data management Detailed understanding of the package environment of all vehicle platforms Change request creation to support vehicle builds

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Standort : Crewe CW1

2022-22988 - Connected Car Engineer

Thu, 02 Nov 2023 09:41:57 Z

Berufsprofil : OPERATIONS/Engineering
Vertragsart : Festanstellung
Beschreibung der Stelle :
The role What you will need Automotive E/E architectures for vehicle control and connected cars services. Exposure to ERA GLONASS / EU / NA / Japan telematics testing. Grey Services – cabin pre-conditioning / remote start Understanding of V2V/V2I communication, eCall, bCall, stolen vehicle tracking (SVT) and cybersecurity. Product delivery for automotive. Automotive safety and cybersecurity standards. Key global connected car eco-system suppliers. Proven supplier management. Self-motivated, and ability to work as a leader and confidently alone. Promote cross functional team working and collaboration between departments. Provide mentorship to junior staff. Conscientious and attention to quality, reliability and safety. Excellent verbal and written communication skills. Excellent personal workload management. Flexible approach to working hours. Masters or bachelor’s degree in Engineering related degree or equivalent experience What you will be doing Produce technical product specifications and cross-functional business process definitions applicable to our connected car features across all production programmes, concept demonstrations & research activities. Produce validation test specifications for all connected car features, including customer orientated road- and track-use, and services that support internal product development, manufacturing, marketing and aftersales. Produce programme gateway work products related to connected cars, including feature definitions, project risks, validation test plans, project timing and costs. Ensure the connected car eco-system is compliant with the applicable global legislation, safety requirements and the highest standards of cyber security and data privacy. Coordinate connected car supplier activities, including cloud-based infrastructure, mobile connectivity, cyber security, data services and IoT applications focused on the customer experience and internal value. Proactive contribution to connected technologies continuous improvements and internal business growth.

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Standort : Crewe