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2026-34957 - Project Engineer Warehouse Operations (production) - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:42 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role This role is integral to the logistics environment where raw materials and components are received, stored, and distributed to various production departments. The warehouse is automated and continuously evolving, requiring a professional who can contribute to its growth and optimization. As part of the Support team, you will collaborate with multiple departments, ensuring the success of production processes through effective project management and operational support. Key responsibilities Lead warehouse projects, including commissioning new freezers or warehouses Validate shipping processes and draft quality agreements with carriers Manage projects end-to-end, including requirement gathering and documentation Act as the point of contact for establishing new flows for cold products Investigate and document quality deviations, defining corrective actions

About you Hold a relevant university degree in fields such as engineering or biomedical sciences Demonstrate strong communication skills and a hands-on mentality Work analytically, using data and collaboration with stakeholders Maintain oversight of various parallel projects and set clear priorities Be a true team player with the ability to resolve operational issues Fluency in both Dutch and English is a must
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34956 - Project Engineer Formulation - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:42 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As a Project Engineer Formulation, you will be specializing in pharmaceutical formulation equipment. A crucial role to ensure a reliable and high-quality supply of medications to patients. You will be part of a multidisciplinary project team, working on equipment upgrades and new constructions related to the formulation step in aseptic production processes. The focus is on safety, compliance, innovation, and cost-efficiency. Your responsibilities will include planning, coordination, specification, design, validation, startup, and supplier interactions to deliver installations on time, within budget, and scope Key responsibilities Take ownership of project activities related to your assigned equipment Monitor project progress and anticipate next steps and phases, including validation Structure complex problems and address them transparently and systematically Communicate proactively with stakeholders in engineering, production, and externally Collaborate and align with stakeholders during meetings and on-site activities

About you Technical/scientific master's degree required: industrial engineer, civil engineer, bio-engineer Experience in a pharmaceutical or GMP environment is a plus Strong validation experience is a significant plus Excellent communication and organizational skills are mandatory Fluency in Dutch and English is a must
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34955 - Project Engineer Filling - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:42 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As Project Engineer Filling, you will join a dynamic team in a pilot plant environment. This role involves supporting the startup of innovative filling lines in a new clinical production plant. The plant focuses on producing the latest pharmaceuticals intended for clinical studies using cutting-edge manufacturing technologies. As part of the startup team, you will have the opportunity to contribute to building an innovative production environment and further develop your skills. You will collaborate with the engineering team to ensure equipment is operational and take responsibility for routine production processes. This position offers a chance to gain deep knowledge of equipment and end-to-end production processes, ensuring production needs are met efficiently Key responsibilities Support project work by developing production processes related to equipment and technology Acquire in-depth knowledge of equipment and end-to-end manufacturing processes Provide hands-on support on the floor and conduct qualification tests Deliver production documentation, including master batch records and procedures Train operators and project engineers on knowledge and procedures

About you Strong project management skills with the ability to lead small projects independently Excellent communication and stakeholder management abilities Critical thinking skills to question and understand technical processes Flexibility to adapt to project needs and meet timelines Technical writing skills for clear documentation and procedure development Fluency in Dutch and English is a must
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34902 - MBR editor - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:42 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role This role is crucial for the introduction of new projects at the launch plant 1. You will be responsible for creating electronic batch records (EBRs) and ensuring high editorial standards across all content outputs. The position requires configuring production processes in the MES system (PAS-X) and translating these processes into a Master Batch Record (MBR). Collaboration with the creative team is essential to assess project needs and maintain brand consistency across company communications. The role involves developing and implementing brand guidelines and overseeing projects from inception to deployment Key responsibilities Create electronic batch records (EBRs) for new projects at the LAUNCH plant 1 Edit and proof content to ensure high editorial standards are met consistently Configure production processes in the MES system (PAS-X) accurately Translate production processes into a Master Batch Record (MBR) in the MES system Collaborate with the creative team to assess project needs and assist with messaging

About you Bachelor's degree or equivalent experience is required for this consultant role Knowledge of MBR design in PAS-X or an equivalent system is essential Strong written and oral communication skills in both English and Dutch are necessary Ability to work independently and in a team, demonstrating good interpersonal skills Capability to translate process-related activities to a Master Batch Record (MBR) independently
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34437 - Project Engineer Formulation Support - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:40 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role We are seeking a Project Engineer Formulation Support to assist the formulation department of our client. Key responsibilities Provide operational support by resolving process or equipment issues Enhance process efficiency by increasing capacity and reducing disruptions Setting priorities, planning and further coordination Develop and share scientific and technical knowledge Project management: communication, planning of resources/budget/facility/business, implementation and evaluation Set up validation documents, test methods, equipment qualification

About you Masters degree in bioengineering, industrial/civil engineering or pharmaceutical sciences Strong analytical and problemsolving mindset Excellent communication and social skills Fluency in Dutch and English
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34435 - Production Engineer - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:40 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
We are seeking a Production Engineer to join our client's versatile production area. About the role: Daily collaboration with Production and Maintenance in order to identify potential quality issues, safety risk, or yield losses. For each identified issue, you will clarify the root of cause, recommend solutions and follow up on the implementation Work closely with Engineering and external partners to implement new equipment/execute major updates to existing equipment Facilitate project meetings to ensure continuous process monitoring and control Lead New Product Introductions from LE/STS - from initiation to completion Serve as the Single Point of Contact (SPOC) for a specific production area you take ownership of

About you Solid technical background Strong organizational and communication skills Preferably experience in automation and equipment validation Familiarity with manufacturing processes and production equipment
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34434 - Project Engineer Formulations - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:40 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role Voor een toonaangevend bedrijf in de farmaceutische sector zijn wij op zoek naar een Project Ingenieur Formulatie. Je werkt binnen een multidisciplinair projectteam aan gevarieerde projecten, gaande van upgrades tot nieuwbouw van equipments gebruikt in de formulatiestap in het aseptisch productieproces. Key responsibilities Verantwoordelijk voor planning, coördinatie, specificatie, design, validatie en opstart van jouw deel van het project Proactief communiceren en rapporteren naar diverse stakeholders binnen engineering en productie Structureren en stapsgewijs aanpakken van complexe problemen en situaties Flexibel aanpassen aan het takenpakket afhankelijk van de projectfase, van documentatie tot machinetesten Samenwerken en afstemmen met stakeholders tijdens meetings en op de werkvloer

About you Jij hebt een technische/wetenschappelijke master (industrieel ingenieur, burgelijk ingenieur, bio-ingenieur... Affiniteit met de farma sector is een must Je beschikt over sterke communicatieve en organisatorische vaardigheden Je kan zelfstandig werken, hebt een kritische blik en bent assertief Een eerste ervaring in een farmaceutische omgeving, met GMP of binnen een asepetische omgeving is een plus
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34433 - Project Engineer Inspection - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:40 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role We are seeking a Project Engineer to join our clients Inspection team. This role requires technical expertise in inspection equipment and technologies used in pharmaceutical production environments. The ideal candidate will have experience in testing, verification, and validation of inspection systems within sterile settings. As Project Engineer, you will be responsible for the engineering of specific inspection installations, including visual inspection machines, leak testers, camera and sensor systems, reject handling, and related automation. The role involves providing technical input within the project team, possessing thorough technical and operational knowledge, and understanding the installation's functionality and compliance requirements. Key responsibilities Develop and document technical specifications, including Engineering Design Specifications and P&IDs Coordinate with Lead Engineer during design, construction, and implementation phases Work according to engineering standards Oversee construction, installation, and commissioning to ensure compliance with specifications Apply project management tools for planning, budgeting, risk management, and stakeholder engagement Manage contractors for the construction, installation, and testing of inspection equipment Ensure accurate documentation of construction, verification, and validation activities within the engineering project file Define and conduct engineering tests, including the verification and validation of inspection equipment Develop validation strategies, test protocols, and verification/validation documents; execute testing procedures and coordinate approvals with Subject Matter Experts (SMEs) and system owners Manage and record deviations and corrective actions (CAPAs), perform risk assessments, review compliance with cGMP standards, and update documentation accordingly

About you Expertise in inspection equipment and technologies for pharmaceutical environments Experience in testing, verification, and validation of inspection systems Ability to develop and document technical specifications and engineering designs Proficiency in project management tools and techniques Strong understanding of compliance requirements and operational functionality
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34430 - Project Engineer Quality Support - Life Sciences - M/F/X

Thu, 30 Apr 2026 22:03:40 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
Binnen Akkodis zijn we op zoek naar een Project Engineer Quality Support voor een van onze klanten in de regio Antwerpen. About the role: In deze rol werk je binnen de ICS Automation afdeling en ben je verantwoordelijk voor het waarborgen van de validatiestatus van computer/computerised systemen. Je biedt operationele ondersteuning en expertise om problemen snel op te lossen. Daarnaast coördineer je validatieprocessen binnen computerprojecten en voer je risicoanalyses uit. Je speelt een cruciale rol in het handhaven van data-integriteit, een steeds belangrijker aspect binnen de farmaceutische industrie. Key responsibilities: Je biedt operationele ondersteuning en advies om software- en infrastructuurproblemen snel op te lossen Je coördineert de validatie van computerprojecten en schrijft validatieplannen en rapporten Je voert risicoanalyses uit en begeleidt projectingenieurs in validatieprocessen Je voert periodieke reviews uit van alle computersystemen om de validatiestatus te waarborgen Je ondersteunt de site bij vragen over data-integriteit en bewaakt de status van geautomatiseerde apparatuur

About you: Een diploma als industrieel, burgerlijk of bio-ingenieur met interesse in softwareontwikkeling en techniek Perfect beheersing van het Nederlands en Engels Sterke interpersoonlijke vaardigheden en communicatieve kwaliteiten Ervaring of interesse in projectgebonden werk, bij voorkeur op een productiesite Het vermogen om een goede balans te vinden tussen compliance en efficiëntie in projecten en processen
Location : Noordkustlaan 16B 1702 Dilbeek

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

Thu, 30 Apr 2026 22:03:30 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

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

Mon, 27 Apr 2026 22:05:40 Z

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

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

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

Mon, 27 Apr 2026 22:05:40 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

Mon, 27 Apr 2026 22:05:40 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

Mon, 27 Apr 2026 22:05:40 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

Mon, 27 Apr 2026 22:05:40 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

Mon, 27 Apr 2026 22:05:39 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

Mon, 27 Apr 2026 22:05:39 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

Mon, 27 Apr 2026 22:05:39 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

Mon, 27 Apr 2026 22:05:39 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

Mon, 27 Apr 2026 22:05:39 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