RSS export of vacancies - Only featured vacancies : No / Business Industry : Life sciences

2024-33147 - Ingénieur validation - (Life Sciences) - F/M/X

Tue, 06 Oct 2026 22:03:11 Z

Category : OPERATIONS/ENGINEERING/PRODUCTION
Contract : Fixed term contract
Position description :
Contexte : Le département Qualification/Validation local du client recherche un(e) consultant(e) pour supporter les projets de développement du site. La mission couvre les activités qualification et validation de l’ensemble des équipements, informatisés ou non. La fonction a pour but de : Assurer la qualification (depuis la phase de Design jusqu'à la fin de la Validation) des équipements, locaux, système informatisés et utilitaires dans le respect des Bonnes Pratiques de Fabrication et des règles d'hygiène et de Sécurité et conformément aux Validation Master Plans System du site. Garantir l’auditabilité permanente des dossiers de validation et de qualification des installations Ce qui se traduit par les activités opérationnelles suivantes : Définir et assurer le suivi des stratégies de qualification / validation Rédiger les documents de qualification / validation dans le respect des Bonnes Pratiques de Fabrication (BPF) Coordonner, exécuter et/ou vérifier les tests de qualification des installations et utilitaires (ex : HVAC, validation thermique, ...) en impliquant les futurs utilisateurs et conformément aux procédures en vigueur. Inclus la gestion des déviations potentielles associées et le suivi des systèmes qualité associés. Etre force de proposition de solutions innovantes et compatibles avec les différents requis chimiques et pharmaceutiques en vigueur et les objectifs de la société.

Profil : Plus de 3 ans d’expérience dans le domaine de la qualification/validation. Connaissance des techniques de qualification/validation d'équipements utilisés en production Capacité à prendre des responsabilités et décisions Une expérience en validation d'équipements de laboratoire est un plus
Location : Brabant Wallon
Minimum level of education required : 5. Bachelor Degree
Language / Level :
French : 4 : Native / Bilingual level
Language / Level :
English : 3 : Advanced

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

Mon, 05 Oct 2026 22:03:53 Z

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

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

2026-35347 - Packaging Engineer - Pharma

Mon, 05 Oct 2026 16:07:44 Z

Category : OPERATIONS/ENGINEERING/PRODUCTION
Contract : Permanent contract
Position description :
Akkodis è un leader globale nel mercato dell'ingegneria e della ricerca e sviluppo, che mira ad accelerare l'innovazione e la trasformazione digitale utilizzando la forza dei connected data. Con la passione per la tecnologia e il talento, il gruppo, composto da più di 40.000 ingegneri ed esperti digitali e con un fatturato di €4bn, offre una profonda esperienza intersettoriale in 28 paesi tra Nord America, EMEA e APAC. La divisione Life Sciences di Akkodis è leader a livello italiano nell’ambito della consulenza ingegneristica, convalida e servizi GMP per le aziende del comparto farmaceutico, chimico e sanitario. Costituita da consulenti specializzati di elevato livello tecnico e provata esperienza nel campo delle Good Manufacturing Practices, che hanno approfondito la loro formazione collaborando con importanti aziende internazionali, l’azienda assicura una totale conformità ai requisiti qualitativi dell’FDA e degli equivalenti organismi europei. I servizi riguardano Engineering, Commissioning & Qualification, IT compliance, Process&Quality, Advanced therapies, training GxP. Ricerchiamo: Packaging Engineer - Pharma Entra a far parte della nostra divisione Life Sciences, un gruppo di oltre 500 consulenti che operano in Italia e circa 5.000 in Europa nelle Life Sciences attraverso le altre Region Europee. La nostra forza è da sempre l’integrazione delle nostre competenze, che ci permettono di avere una visione a 360° del mondo farmaceutico. Quale sarà il tuo contributo in Akkodis? Entra a far parte del nostro Team di Packaging Engineering e contribuisci in prima persona a promuovere innovazione, qualità e sostenibilità nelle nostre attività di packaging! Ti occuperai di: Fornire leadership tecnica e gestire progetti nell'ambito del Packaging Engineering Garantire supporto tecnico globale sulle attività di packaging, con particolare focus sulla gestione di artwork/grafica e sulla progettazione del packaging secondario e terziario Coordinare le attività di convalida dei processi di confezionamento (PPQ - Process Performance Qualification) e gli studi di qualifica per la distribuzione (test ASTM) presso le Contract Manufacturing Organizations (CMO) Gestire la documentazione MSAT (Manufacturing Science and Technology), inclusi protocolli di validazione, specifiche tecniche, valutazioni del rischio e report di technology transfer Collaborare con team multidisciplinari quali Ingegneria, Qualità, Operations, Regulatory Affairs, Procurement e altre funzioni globali, garantendo una corretta esecuzione dei progetti Lavorare a stretto contatto con i fornitori di materiali di confezionamento, promuovendo l'innovazione e lo sviluppo di soluzioni di packaging sostenibili

Hai una Laurea in ambito Tecnico/Industriale ed almeno 3 anni di esperienza in Packaging Engineering? Candidati ed entra a far parte di un Team che progetta soluzioni di packaging in grado di migliorare la sicurezza dei pazienti e promuovere la sostenibilità! About you Requisiti per iniziare il tuo percorso di crescita: Background in Packaging Engineering Esperienza in Packaging Technical Operation Esperienza in artwork/grafica, packaging secondario e terziario Ottime competenze di Project Management Passione per la qualità, efficienza e continuous improvement Lingua inglese fluente, sia scritta e parlata (almeno livello B2) Ottima conoscenza della lingua italiana (almeno livello C1) Disponibilità a trasferte internazionali Offerta Contratto a tempo indeterminato CCNL Commercio RAL a partire da 34.000 € in base all'esperienza ed alle competenze della persona Cosa troverai in Akkodis? Un percorso di carriera strutturato e personalizzato, con possibilità di crescita verticale e trasversale Ti supporteremo grazie ai nostri piani di formazione, ad una performance review annuale, ad un affiancamento nelle fasi iniziali di ingresso, unitamente a follow-up con figure Manageriali e HR Business Partner Avrai a disposizione una Piattaforma di Corporate Benefits Location Basso Lazio, attività gestibile da remoto per il 70% del tempo
Location : Basso Lazio, attività gestibile da remoto per il 70%
Minimum level of education required : 5. Bachelor Degree

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

Sun, 04 Oct 2026 22:04:12 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

Sun, 04 Oct 2026 22:04:12 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

Sun, 04 Oct 2026 22:04:12 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

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

Sun, 04 Oct 2026 22:04:12 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

2025-34556 - Electrical engineer - (Life Sciences) - F/M/X

Sun, 04 Oct 2026 22:04:11 Z

Category : OPERATIONS/ENGINEERING/PRODUCTION
Contract : Permanent contract
Position description :
Description du rôle : Pour renforcer nos équipes de chantiers, nous recherchons une personne avec une bonne expérience de la gestion/ organisation/ préparation de chantiers électriques avec une bonne flexibilité au changement/ à l'imprévu. La réactivité de cette personne doit être assurée pour maintenir les équipes au travail en assurant la sécurité. Vos responsabilités : Depuis la livraison des plans jusqu’à la réception des travaux : Maîtriser les règles et les normes. Analyser les plans et les schémas de l’installation électrique réalisés par le bureau d’études. En fonction de son analyse du terrain, il peut proposer des améliorations aux plans d’installation. Définir la méthode de réalisation des travaux (au besoin en collaboration avec le Bureau d’études et/ou le Chargé d’affaires). Organiser, planifier le travail de l’équipe et gérer les moyens matériels d'exécution Faire respecter les règles de sécurité (pré-start meeting / LMRA / permis de travail .... Faire le lien entre le client et le besoin. Faire la mise en service et contrôler la qualité des installations. N'hésitez pas à partager votre cv par message privé ou à m'envoyer un e-mail sur : Fatima-ezzahra.choukri@akkodis.com

Votre profil : Lecture de plans électriques, maitrise Excel , un savoir-faire à transmettre aux équipes et une identification des moyens pour exécuter le travail. Grande rigueur, motivé, professionnalisme, respect des délais, travail en équipe, ouvert à la communication. Maîtrise des normes et des consignes de sécurité. Solides compétences en électricité (pour travailler dans le secteur pharmaceutique.) Compétences en management. Réactivité et sens de l’anticipation. Capacité d’adaptation. Sens du relationnel.
Location : Belgique
Language / Level :
English : 3 : Advanced
Language / Level :
French : 3 : Advanced

2025-34552 - Construction manager - (Life Sciences) - F/M/X

Sun, 04 Oct 2026 22:04:11 Z

Category : OPERATIONS/ENGINEERING/PRODUCTION
Contract : Permanent contract
Position description :
Vous serez responsable de la gestion quotidienne et du suivi des chantiers de construction et de démolition. Véritable expert technique, il veille à la bonne exécution des projets, joue un rôle clé dès la phase d’étude et supervise le site pendant toute la durée des travaux. Il garantit également le respect des normes de sécurité. Vos responsabilités 🎯 : Assurer la responsabilité globale du suivi et de l’organisation des activités de construction et de démolition liées au projet. Préparer et mettre à jour le plan global de construction et de démolition coordonnant toutes les activités. Mettre à disposition les ressources nécessaires tout au long des phases de construction et démolition afin de respecter les jalons fixés. Vérifier la compétence et la préqualification des concepteurs, contractants et autres membres de l’équipe en matière d’EHS (Environnement, Hygiène et Sécurité). Garantir que les entreprises exécutent le projet en toute sécurité, conformément aux réglementations locales et aux exigences de l’entreprise. Définir avec le responsable EHS du site les responsabilités et obligations en matière de sécurité. Promouvoir et soutenir une culture EHS en ligne avec les valeurs de l’entreprise. Rédiger le Construction Safety Plan (CSP) initial pour informer les contractants. S’assurer que tous les travailleurs bénéficient d’une formation sécurité spécifique au chantier. Veiller à la mise à jour régulière du CSP par les contractants. Mettre en place un processus d’assurance performance EHS via un programme d’audits, d’observations et d’interactions. S’assurer de l’existence d’un programme EHS proactif, favorisant la reconnaissance et la responsabilisation. Contacts : N'hésitez pas à partager votre cv par message privé ou à m'envoyer un e-mail sur : fatima-ezzahra.choukri@akkodis.com

Votre profil 👤: Master en Génie civil ou industriel (construction, EHS, etc.). Expérience confirmée en gestion de projets (Capex et non-Capex) et solide bagage technique (construction, HVAC, facilities, utilités, tuyauteries blanches/noires, EHS, etc.). Expérience dans la gestion de chantiers en environnements exigeants : pharmaceutique, chimique, nucléaire ou agroalimentaire. Capacité à établir et maintenir un véritable partenariat avec les équipes et les différents départements. Compétences 💪 : Compétences éprouvées en gestion de multiples parties prenantes. Excellente adaptabilité, de l’opérateur terrain jusqu’aux cadres dirigeants. Solides compétences en gestion du changement. Certification PMP et/ou Prince2 appréciée. Maîtrise du français et de l’anglais. Contacts : N'hésitez pas à partager votre cv par message privé ou à m'envoyer un e-mail sur : fatima-ezzahra.choukri@akkodis.com
Location : Belgique
Minimum level of education required : 6. Master Degree
Language / Level :
French : 3 : Advanced
Language / Level :
English : 3 : Advanced

2025-34551 - Project Manager Capex - (Life Sciences) - F/M/X

Sun, 04 Oct 2026 22:04:11 Z

Category : OPERATIONS/PROJECT MANAGEMENT
Contract : Permanent contract
Position description :
En tant que Project Manager Capex, vous serez responsable de la planification, de l’exécution et de la clôture des projets d’investissement (Capex) au sein de l’organisation. Vous travaillerez en étroite collaboration avec des équipes transverses afin de garantir la livraison des projets dans les délais, le respect du budget et la conformité aux standards qualité et réglementaires. Responsabilités : Gérer l’ensemble du cycle de vie des projets Capex, de l’initiation à la clôture. Élaborer des plans de projet détaillés (objectifs, plannings, ressources, budgets). Coordonner les activités entre les équipes internes et les partenaires externes pour une exécution efficace. Suivre l’avancement des projets et fournir des rapports réguliers sur le statut, les risques et les opportunités. Identifier et gérer les risques associés aux projets, et mettre en œuvre les plans de mitigation appropriés. Assurer la conformité avec les réglementations et standards qualité de l’industrie pharmaceutique. Participer à la gestion du changement et à la résolution de problèmes tout au long du cycle de vie du projet. Collaborer avec les départements R&D, production et qualité afin de garantir l’alignement des projets avec les objectifs stratégiques de l’entreprise. Contacts : N'hésitez pas à partager votre cv par message privé ou à m'envoyer un e-mail sur : fatima-ezzahra.choukri@akkodis.com

Diplôme en ingénierie, gestion de projet, sciences pharmaceutiques ou domaine connexe. Expérience confirmée dans la gestion de projets Capex, idéalement dans le secteur pharmaceutique ou biopharmaceutique. Connaissance des réglementations et standards de l’industrie pharmaceutique. Excellentes compétences en communication et en leadership. Capacité à travailler sous pression et à gérer plusieurs projets simultanément. Maîtrise des outils de gestion de projet (MS Project, Primavera, etc.). Une certification en gestion de projet (PMP, PRINCE2, etc.) constitue un atout.
Location : Belgique

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

Sun, 04 Oct 2026 22:04:11 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

Sun, 04 Oct 2026 22:04:11 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

Sun, 04 Oct 2026 22:04:11 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

Sun, 04 Oct 2026 22:04:10 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

Sun, 04 Oct 2026 22:04:10 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

Sun, 04 Oct 2026 22:04:10 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

Sun, 04 Oct 2026 22:04:10 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

Sun, 04 Oct 2026 22:04:10 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

Sun, 04 Oct 2026 22:04:10 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

Sun, 04 Oct 2026 22:04:10 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