RSS export of vacancies - Only featured vacancies : No / District : Belgium-->Flanders-->Antwerp

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

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

Mon, 28 Sep 2026 22:06:44 Z

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

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

2026-35096 - QC Analyst - Life Sciences - M/F/X

Mon, 28 Sep 2026 22:06:44 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As QC Analyst, you will support laboratory operations focused on incoming materials and in-process samples. You will manage and test a range of primary and secondary components, as well as samples from in-process products, special tests, SQA, and MS&T. You will perform and document analytical measurements according to GLP and cGXP requirements while working in compliance with DI principles. The position combines hands-on laboratory work, data integrity responsibilities, and a strong focus on quality, safety, and continuous inspection readiness. Key responsibilities Manage samples for incoming inspection, including primary and secondary components and materials from in-process products, special tests, SQA, and MS&T departments. Perform and document measurement tests on incoming and in-process samples in accordance with Good Laboratory Practices and applicable laboratory procedures. Maintain familiarity with and correctly apply the different measurement techniques used in the laboratory, ensuring consistent and reliable analytical results. Contribute to maintaining constant inspection readiness by following procedures, completing documentation accurately, and supporting audit-related activities when needed. Work according to established HSE safety procedures, detect and report potential incidents and risks, and propose practical solutions to reduce or eliminate these risks. Support laboratory investigations as required and, when assigned, take on responsibilities such as instrument owner, including being the point of contact for instrument issues and coordinating maintenance. Contribute to optimization projects related to laboratory operations, with focus on efficiency, quality, and data integrity, and support implementation of agreed improvements. Work to minimize lab errors, incidents, and invalid analyses due to human error, and support a culture of Right First Time (RFT) in both execution and documentation. Help keep IIA and WIP under control by understanding planning and priorities and acting accordingly to meet established deadlines without creating backlogs.

About you Practical experience or strong affinity with performing and documenting laboratory measurement tests in compliance with GLP requirements. Understanding of cGXP requirements and DI principles, with the ability to apply these consistently in daily laboratory work and documentation activities. Capability to become or act as SME (Subject Matter Expert) for specific analytical or measurement techniques and to support colleagues with technical questions. Strong focus on quality and accuracy, with the ability to work according to Right First Time (RFT) principles and minimize lab errors and invalid analyses. Awareness of HSE requirements and safe laboratory practices, including the ability to detect, report, and help resolve potential safety risks or incidents. Willingness to take on additional responsibilities such as instrument owner, On The Job Trainer, mentor, SOP reviewer using GdoC P software, archive owner, Data Integrity Expert/champion, or Safety Champion when assigned. !! Fluency in Dutch and English
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34940 - Junior packaging engineer - Life Sciences - M/F/X

Mon, 28 Sep 2026 22:06:44 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As Junior Packaging engineer, you will support the development and implementation of packaging solutions. You will participate in technical meetings, documentation of processes, and conducting root cause investigations. You have a strong understanding of pharmaceutical manufacturing processes and regulatory requirements, and will contribute to customer satisfaction by adhering to strict procedures and staying informed on industry trends. Key responsibilities Draw up documents according to specific guidelines based on technical information Participate in technical meetings and gather necessary information Facilitate and close out root cause investigations and document findings Report on metrics and contribute to customer satisfaction Follow customer procedures strictly and stay informed on industry trends

About you Knowledge of pharmaceutical manufacturing processes and products Understanding of Quality & Compliance regulatory requirements (GMP/EH&S) Familiarity with manufacturing site systems and procedures Knowledge of secondary and tertiary packaging materials Proficiency in cGxP and adherence to EH&S procedures
Location : Noordkustlaan 16B 1702 Dilbeek

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

Mon, 28 Sep 2026 22:06:43 Z

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

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

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

Mon, 28 Sep 2026 22:06:43 Z

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

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

2025-34685 - HVAC validation analyst - Life Sciences - M/F/X

Mon, 28 Sep 2026 22:06:43 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role Within our client's production departments, raw materials are transformed into filled medicines. The product goes through several manufacturing steps (weighing, formulation, preparation, lyophilization, filling, capping, inspection, storage, and transport). At every stage, production strives for the highest level of operational excellence. AS HVAC Validation Analyst, you will work within the Utilities Department. The HVAC Validation team is responsible for the timely execution of validation activities for equipment and rooms related to product storage (refrigerators, freezers, climate chambers, warehouses, freeze dryers, incubators, etc.), as well as the validation of the cooling and ventilation systems (HVAC) themselves. Key responsibilities Independently plan, monitor, and execute routine validation programs for validation studies of equipment, HEPA filters, laboratory and production devices, and temperature-controlled areas within the site. Prepare validation worksheets and ensure their approval and classification according to the appropriate procedures. Enter and manage all validation data in the dedicated validation software. Initiate and follow up on quality deviations; report deviations observed during validation studies. Collaborate and coordinate with various departments Ensure the continuous availability of validation equipment. Monitor and correctly process validations carried out by external companies.

About you Bachelor’s degree in a scientific discipline or equivalent experience. Good command of English (written and spoken). Strong interpersonal skills and a team-oriented attitude. Excellent communication and organization skills. Analytical mindset with problem-solving abilities.
Location : Noordkustlaan 16B 1702 Dilbeek

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

Mon, 28 Sep 2026 22:06:43 Z

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

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

2025-34607 - Construction supervisor - Life Sciences - M/F/X

Mon, 28 Sep 2026 22:06:43 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role You will be involved in a civil construction project. The role requires a professional with a strong safety mindset and experience in the pharmaceutical sector or a similar industry. The project is in the civil construction phase, involving equipment installation, utilities, and HVAC systems, with some exposure to automation. You will work closely with discipline engineers and the Construction Manager to ensure the successful execution of the project. Key responsibilities Organize and oversee daily activities on the construction site to ensure smooth operations Evaluate project progress daily and address any planning conflicts with the project team Prepare and release necessary work permits in collaboration with contractors Conduct task risk analyses with contractors as part of the work permit process Organize regular site coordination meetings with the Safety Supervisor and team leaders

About you Proven experience in civil construction supervision, preferably in the pharmaceutical sector Strong understanding of safety protocols and risk management in construction Ability to evaluate project progress and identify potential conflicts Experience in organizing and conducting site coordination meetings Excellent communication skills to guide contractors and collaborate with project teams
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34606 - Construction supervisor Building Electricity & Security - Life Sciences - M/F/X

Mon, 28 Sep 2026 22:06:43 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As a Construction Supervisor Building Electricity & Security (BES) you will oversee electrical and security-related construction works within F&U projects. This role is crucial in ensuring the safe execution of installations, maintaining compliance with technical standards, and delivering high-quality results within the defined planning and budget. Key responsibilities Coordinate and monitor electrical and security construction works to ensure compliance with technical standards Prepare and manage daily planning for electrical and security contractors, aligning with other disciplines Ensure quality and safety by preparing permits and managing LOTO procedures on construction sites Provide technical support during critical phases and resolve technical issues in consultation with contractors Prepare and monitor commissioning of systems, ensuring proper delivery of As-Built documentation

About you Bachelor in Electromechanics, Electricity, or equivalent through experience At least 8 years of experience in industrial E&I projects Certificates: VOL-VCA, BA4, BA5 Knowledge of HV/LV installations and security systems is essential Strong communication skills in Dutch and English
Location : Noordkustlaan 16B 1702 Dilbeek

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

Mon, 28 Sep 2026 22:06:43 Z

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

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

2025-34778 - Project Engineer Launch Excellence - Life Sciences - M/F/X

Sat, 26 Sep 2026 22:05:32 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
The Project Engineer Launch Excellence role is pivotal in managing all validation aspects associated with the introduction of new products at the site. The position involves a comprehensive range of activities essential for successful implementation and ensuring regulatory compliance throughout the product lifecycle. Ideally, you possess a strong scientific background and demonstrate expertise in validation processes, risk assessments, and project management. You are proactive and possess the ability to work both independently and collaboratively within a team. Key responsibilities Validate and document support for formulation, filling, transport, and packaging processes Conduct urgent quality investigations, including root-cause analyses and corrective actions Perform comprehensive risk analyses and define appropriate mitigation measures Support and implement process and system changes necessary for product introduction Manage projects, including coordination, planning, problem-solving, milestone tracking, and progress reporting

About you Master’s degree in bioengineering, pharmaceutical sciences, biochemistry, or biotechnology Fluency in botch Dutch & English (both spoken and written) Strong communication and interpersonal skills with a team-oriented mindset Organized, precise, and quality-conscious work style with strong analytical skills Experience in executing validation projects and proficiency in planning and project coordination
Location : Noordkustlaan 16, 1702 Dilbeek

2025-34777 - Project Engineer Integration - Life Sciences - M/F/X

Sat, 26 Sep 2026 22:05:32 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
As a Project Engineer intergation, you will join the Level 2 Integration team. The role involves working within the Engineering department, which is responsible for delivering investment projects on time and within budget. The team ensures installations are robust and efficient, producing high-quality products. The position requires collaboration from project definition through production startup, with a focus on automation and integration. It includes optimizing systems and processes using modern technology, including equipment and installation HMIs, SCADA, and further integrations within the automation concept Key responsibilities Implement requested changes from new projects and support existing installations Ensure the Alert system evolves with the site and remains current Coordinate with equipment suppliers to meet integration needs Develop Engineering Specifications to facilitate integration Collaborate with Engineering Equipment Project Engineers and other stakeholders

About you Experience in an industrial automation environment (within pharmaceutical environment is a plus) Excellent proficiency in Dutch and English languages Strong knowledge of database tools and software principles Familiarity with network protocols and PLC, SCADA/HMI software Analytical, methodical, and problem-solving skills with strong communication abilities
Location : Noordkustlaan 16, 1702 Dilbeek

2025-34776 - Master planner & scheduler

Sat, 26 Sep 2026 22:05:32 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As a Master Planner & Detailed Scheduler, you will ensure the seamless operation of production schedules and inventory management. You are responsible for creating and maintaining a master production schedule, resolving manufacturing challenges, and optimizing production processes. This position requires a strategic thinker with a strong background in supply chain management and the ability to collaborate effectively with various business partners. Key responsibilities Create and maintain a constrained weekly master production schedule for all production requirements Update and maintain the actual production schedule within the appropriate scheduling horizon Perform site/portfolio capacity planning in terms of resources, shifts, equipment, and shutdowns Maintain material inventories within target, minimizing excess, obsolete, and expired products Collaborate with operations to ensure accurate supply and capacity parameters

About you Min of a Bachelor's degree or equivalent experience is required In-depth experience with SAP/OMP+ is preferred for effective schedule management Ability to analyze data to identify and resolve exceptions, minimizing supply disruptions Strong intuition for business in supply chain and financials Proven ability to build strong collaborative teams and relationships
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34775 - Project Engineer Validation Coordination - Life Sciences - M/F/X

Sat, 26 Sep 2026 22:05:32 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role De Project Validation Coordinator (VALCO) ondersteunt de projectleider bij het coördineren van het projectteam om de gedefinieerde projectdoelstellingen te behalen met betrekking tot validatie. In deze rol ben je verantwoordelijk voor het opstellen, consolideren en bewaken van het volledige validatieprojectplan en -rapport. Je licht de validatiestrategie toe aan het projectteam, het management en eventuele inspecteurs en fungeert als inhoudelijk aanspreekpunt voor alle validatiegerelateerde aspecten binnen het project. Je volgt de vooropgestelde validatiestrategie nauwgezet op, stuurt waar nodig bij of escaleert tijdig, en bewaakt de impact op de projecttiming. Je coacht project engineers op vlak van validatie en kwaliteitssystemen, ziet toe op correcte toepassing van good validation practices en bewaakt de kwaliteit van de opgeleverde documenten. Daarnaast faciliteer en documenteer je risicobeoordelingen binnen het kwaliteitssysteem en lever je input voor managementrapporteringen. In deze brugfunctie werk je nauw samen met Engineering, Quality, technische specialisten (SME’s), System Owners en andere betrokkenen. Binnen de projectstructuur neem je de rol op van subteamlead Validation. Naast validatiecoördinatie bied je ondersteuning aan de projectleider bij het bewaken van de algemene projectplanning. Je stelt de overkoepelende projectplanning op, consolideert alle mijlpalen en houdt het centrale projectplanningsbestand up-to-date. Je monitort continu de voortgang, informeert het projectteam tijdig over status en knelpunten en signaleert mogelijke conflicten of risico’s in de uitvoering en onderlinge afhankelijkheden van projectactiviteiten. Je ondersteunt de projectleider bij het identificeren en beoordelen van planningsrisico’s en het opstellen van passende mitigerende acties. Ook op dit vlak lever je input voor rapportering naar het management.

About you Relevant experience Fluent in Dutch and English Good communication skills
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34774 - Project Engineer Transport & Handling equipment - Life Sciences - M/F/X

Sat, 26 Sep 2026 22:05:32 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role For a leading engineering site in Puurs, we are seeking a Project Engineer specializing in Transport and Handling Equipment. This role is integral to the automation and enhancement of logistics processes, supporting the delivery of high-quality injectable pharmaceuticals. As our clients site expands, there is a growing need to evolve surrounding processes for material supply to production departments, enhancing efficiency and establishing just-in-time delivery systems. The Project Engineer will play a pivotal role in automating processes, from robotization of manual tasks to optimizing pallet transport and vial handling. Key responsibilities Develop and monitor project plans for multiple equipment packages Identify potential risks related to safety, breakdowns, and operability Manage stakeholder relationships across various departments Report progress to project teams and management at regular intervals Draft equipment specifications and coordinate with suppliers Serve as the primary contact for equipment suppliers Align production department needs with project objectives Organize and attend equipment Factory Acceptance Tests (FATs) Oversee installation, testing, verification, and commissioning of equipment Prepare and deliver necessary project documentation

About you Master's degree in Industrial Engineering, Civil Engineering, Bioengineering, or equivalent A first experience in a related role is necessary Proficiency in both Dutch and English languages is mandatory Excellent organizational, communication and documentation skills Teamplayer Knowledge of robotics and automation is a plus
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34991 - Equipment Automation Project Engineer - Life Sciences - M/F/X

Thu, 24 Sep 2026 22:02:41 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As Equipment Automation Project Engineer, you will join a dynamic team in a newly established pilot plant. This facility is dedicated to producing cutting-edge pharmaceuticals for clinical studies using the latest aseptic manufacturing technologies. The production process includes formulation, preparation, filling, and freeze-drying. As part of the startup team, you will have the opportunity to contribute to building an innovative production environment and advance your technical skills. This role involves supporting the project and production teams in understanding and optimizing various equipment, ensuring smooth operations from the engineering phase through routine production Key responsibilities Support project work by executing tests during equipment commissioning and qualification Understand the production process and equipment through hands-on experience and design documents Troubleshoot mechanical, electrical, or automation-related issues independently Develop smaller mechanical or programmatic designs to enhance process robustness Learn PLC and software integration of the equipment for seamless operations

About you Bachelor’s degree in Electromechanical Engineering or Master’s in Industrial or Civil Engineering Minimum of 2 years of work experience, preferably in the pharmaceutical or food industry Proficiency in HMI (SCADA WinCC) and basic PLC systems (Siemens, Rockwell) BA4/BA5 training and Six Sigma certification (Green or Yellow Belt) are advantageous Fluent in both Dutch and English, with strong communication skills
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34990 - Black Utilities Engineer - Life Sciences - M/F/X

Thu, 24 Sep 2026 22:02:41 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role This role involves managing and designing projects related to Black Utilities, including systems such as ice water, cooling water, heating water, glycol, city water, compressed air, drains, heat pumps, cooling towers, and steam boilers. You will be responsible for overseeing multiple projects simultaneously, ensuring quality, safety, and adherence to timelines. This position requires a deep understanding of mechanical and process design, as well as the ability to provide input and conduct reviews. The role also involves procurement, on-site construction supervision, commissioning, and system handover Key responsibilities Develop and manage the planning for multiple concurrent projects with a focus on Black Utilities Design Black Utilities projects, including concept, basic, and detail design phases Provide input for mechanical design, including P&ID, 3D modeling, sizing, and calculations Create process designs, including functional descriptions, interlocks, alarms, and parameters Prepare RFQs and manage procurement for relevant project packages Supervise on-site construction with attention to quality, safety, and scheduling Commission and verify systems to ensure proper functionality Transfer systems to the internal client upon completion

About you Fluency in Dutch language for effective communication and documentation Expertise in Black Utilities systems, including ice water, cooling water, and steam boilers Strong ability to manage multiple projects simultaneously with attention to detail Experience in mechanical and process design, including P&ID and 3D modeling Capability to conduct reviews and provide input for design and process improvements
Location : Noordkustlaan 16B 1702 Dilbeek