RSS export of vacancies - Only featured vacancies : No / Country : Belgium / District : Belgium-->Wallonia-->Hainaut, Belgium-->Wallonia-->Walloon Brabant

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

Thu, 21 May 2026 22:03:21 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

Thu, 21 May 2026 22:03:21 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

Thu, 21 May 2026 22:03:21 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

2026-34939 - Project Lead substations Oost- en West-Vlaanderen - Energy - M/F/X

Thu, 21 May 2026 22:03:21 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As a Project Leader for electrical infrastructure projects, you will be operating in the regions of East and West Flanders. This role involves managing projects related to substations with voltage levels of 380, 220, 150, 70, and 36 kV. The Project Leader will be responsible for defining, studying, designing, and ensuring the execution of projects from inception to commissioning and administrative closure. Key responsibilities Define, study, and design electrical infrastructure projects for substations Manage project budgets, planning, and reporting to team leaders Collaborate in the preparation of tender documents and participate in procurement processes Lead and coordinate project execution on-site with involved entities Ensure autonomous completion of tasks with reporting to the Manager

About you Degree in electrical engineering or electromechanical engineering Experience in project management; recent graduates are welcome to apply Knowledge of high-voltage systems is essential Strong sense of responsibility and organizational talent Excellent communication skills in Dutch; French is advantageous but not required
Location : Noordkustlaan 16B 1702 Dilbeek

2026-34938 - Project Engineer Water - Energy - M/F/X

Thu, 21 May 2026 22:03:20 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As Project Engineer Water, your role is pivotal in designing major marine infrastructure projects, ensuring high-quality and standards-compliant solutions for complex water-related structures. The position involves technical design responsibilities, multidisciplinary coordination, client interaction, and project follow-up from concept to completion. You will lead the design of assigned components within large marine infrastructure projects and act as a technical point of contact for various stakeholders, including clients, joint venture partners, engineering consultancies, subcontractors, and contractors. Key responsibilities Lead the design of components within large marine infrastructure projects, ensuring compliance with standards Act as a technical point of contact for clients and partners, facilitating effective communication Produce designs for port master planning, locks, quay walls, jetties, and other structures Analyze and optimize installation methods, exploring innovative solutions Coordinate and coach engineers and CAD designers, verifying drafting work

About you Master of Science in Structural Engineering with a focus on marine engineering Proficient in Dutch, with good knowledge of English or French At least 2 years of relevant design experience in marine infrastructure Strong knowledge of Belgian and European standards and public sector contract management Experience with SCIA Engineer, Plaxis, GeoStudio, or DSheet Piling is a plus
Location : Noordkustlaan 16B 1702 Dilbeek

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

Thu, 21 May 2026 22:03:20 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

Thu, 21 May 2026 22:03:20 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

Thu, 21 May 2026 22:03:20 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

Thu, 21 May 2026 22:03:20 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

Thu, 21 May 2026 22:03:19 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

Thu, 21 May 2026 22:03:19 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

Thu, 21 May 2026 22:03:19 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

2025-34509 - Operations Advanced Support Supervisor - Life Sciences - M/F/X

Thu, 21 May 2026 22:03:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role An Operations Advanced Support Supervisor will oversee the support operations team responsible for production support activities, including Grade B cleaning, Material Transfer, Replenishment and Sterilization. The role involves managing aspects of the CAR-T process operations, ensuring safe and compliant manufacturing operations in line with cGMP requirements. The position operates on a 4/4 shift system with 10-hour shifts. Key responsibilities Act as a SME for quality aspects related to production activities Manage and review documentation in Production zones, including batch records and SOPs Lead and coordinate production support activities, optimizing schedules for compliance Support Tech Transfer plans for new production introductions and process optimizations Implement and lead Tier 1 and Tier 2 meetings to ensure clear communication Ensure safe and compliant operations according to EHS and cGMP

About you Bachelor or Master in science, bio-engineering, pharmacy or related field Min of 1 year in a cGMP or ATMP environment Min of 5 years of direct people management, overseeing teams of 10+ individuals Proficiency with Microsoft Office tools, MES/EBR knowledge is a plus Fluency in English and Dutch Ability to accommodate shift work, including evenings and weekends as required
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34499 - Operations Advanced Supervisor - Life Sciences - M/F/X

Thu, 21 May 2026 22:03:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As supervisor, you will manage a team of approximately 30 members, including process operators, cleanroom leads, badge record reviewers and experts. Responsibilities include overseeing daily operations, conducting one-on-one and evaluation meetings, participating in recruitment interviews, and collaborating with schedulers for planning. The position operates on a 4/4 shift system with 10-hour shifts. Key responsibilities Manage operational teams and supervise various units within the CAR-T production process Ensure strict compliance with cGMP standards and manage quality aspects Collaborate with other departments to resolve production issues effectively Oversee and review critical documentation such as procedures and work instructions Supervise the release and review of batch records for quality control

About you Preferably a PhD or Masters degree in science, bio-engineering, pharmacy or other related fields Min 3 years of experience in a GMP or ATMP environment (preferably within the pharmaceutical or biotech industry) Knowledge regarding cGMP regulations and clean room operations is an advantage Familiarity with MES (Manufacturing Execution Systems) & ERB (Electronic Batch Record) is a plus You are fluent in English (spoken & written)
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34486 - Quality project associate - Life Sciences - M/F/X

Thu, 21 May 2026 22:03:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As a Quality project associate, you will ensure product quality and compliance within Quality Operations. The position involves overseeing product-related qualifications and validations, ensuring regulatory Chemistry, Manufacturing & Controls (CMC) compliance, and facilitating successful product launches. The specialist will act as an independent quality authority, focusing on validation, registration, and implementation processes. This is an opportunity to contribute to the excellence of product launches and regulatory compliance in a dynamic environment Key responsibilities Act as the quality authority for product-related qualifications and validations, ensuring compliance with cGMPs Oversee process qualification, method validation, and component qualification for assigned products Ensure regulatory CMC compliance by reviewing registration dossiers and site practices Conduct data verification and QA review for marketing authorization filings and variations Implement approved regulatory changes timely and accurately across different markets

Your Skills Possess a Master's degree in a scientific discipline such as Pharmacy or Biomedical Sciences Min 2 years of experience in the pharmaceutical or medical device industry Excellent analytical and problem-solving skills in a quality assurance context Exhibit strong oral and written communication skills in both Dutch and English Maintain a thorough understanding of cGMP, regulatory guidances, and medical device regulations
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34485 - Business Analyst - Life Sciences - M/F/X

Thu, 21 May 2026 22:03:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role We are seeking a Business analyst with expertise in industrial automation and software development. This role involves managing multiple projects within a Scrum framework, providing UX/UI guidance, and performing Computer Systems Validation (CSV) and Computer Systems Assurance (CSA) activities. The candidate will have a strong analytical mindset and the ability to work independently while collaborating with external parties on process automation projects. This position requires excellent communication skills in Dutch and English and offers the opportunity to work in a dynamic environment focused on innovation and efficiency. Key responsibilities Monitor project scope, objectives, and planning within a Scrum framework Provide UX/UI expertise and guidance on ongoing projects Perform Computer Systems Validation (CSV) and Computer Systems Assurance (CSA) activities Define test scenarios and express them using Gherkin syntax Draft qualification protocols and participate in software testing, including headless applications Conduct risk assessments Provide second-line support during daily operations

About you Master’s or Bachelor’s degree in Computer Sciences or Automation, or equivalent experience Minimum of 3 years of experience in an industrial automation environment Minimum of 3 years of experience in software development Strong analytical skills, structured mindset, and innovative thinking Experience in writing functional specifications and executing automation projects Fluent in Dutch and English (verbal & written)
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34482 - Project Engineer Building Electricity & Safety - Life Sciences - M/F/X

Thu, 21 May 2026 22:03:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the rol This role involves working on projects that focus on the development and maintenance of electricity systems, including low and high voltage, network infrastructure, gas monitoring systems, and lighting. Additionally, the position encompasses security systems such as CCTV, access control, and fire detection. The Project Engineer collaborates with the Technical Owner to find optimal solutions that balance quality and budget, with a strong emphasis on safety. Key responsibilities Collaborate with multidisciplinary team to align project scope, planning and budget Guide third-party contractors in the execution of project tasks and responsibilities Prepare detailed technical specifications and scope of work documents Manage the sourcing and appointment of contractors, coordinating with procurement as needed Oversee contractor activities and ensure compliance with project requirements

About you Master's degree in electrical or electromechanical engineering VCA certification for supervisors, knowledge of Caneco software and experience with drawing tools (Eplan or AutoCAD) A first experience in the pharmaceutical industry and/or demonstrable experience working with electricity/security at an industrial level is a plus Fluency of Dutch and English
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34453 - Sub Team Lead Utilities - Life Sciences - M/F/X

Thu, 21 May 2026 22:03:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role As Sub Team Lead Utilities, you will participate in major investment projects within laboratory settings, focusing on chemical and microbiological labs. You will be responsible for organizing, coordinating, and managing the design, construction, installation and validation of various utilities (ex: lab water, lab gases, compressed air, vacuum, heating and cooling water, HVAC and electricity). Key responsibilities Collaborate with project leads and team members to ensure project success Monitor and manage technical content of laboratory projects Define project roles based on timeline, workload and required skills Effective communication with stakeholders regarding the resources (staff & tools) working on project

About you Master's degree in a technical/scientific field 10 years of experience in project management and/or leading engineering teams Strong technical, organizational and leadership skills Excellent oral, written and interpersonal communication skills, also including presentation abilities
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34450 - Production Support Engineer - Life Sciences - M/F/X

Thu, 21 May 2026 22:03:19 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role Currently seeking a Production Support Engineer to join our client's CAR T Techlance facility, in order to increase production capacity. A multidisciplinary position, where you will be involved in the design, maintenance and continuous improvement of well-defined operational support activities within manufacturing. Key responsibilities Facilitate communication between Ghent operations and pre-processing activities to optimize processes Drive continuous improvement; track and analyze Key Performance Indicators to assess production efficiency and material usage Develop and approve operational documentation framework, including procedures and work instructions Conduct operational assessment changes Participate in Change Control/Technical Board meetings focusing on continuous improvement Contribute to root cause investigations and develop robust CAPA plans

About you Master in an engineering or scientific discipline, or equivalent through experience Preferably 10 years of experience in MSAT, quality or operations Fluent in both Dutch and English Experience with project management or training is an advantage Willingness to work 5 days/week on site; limited home work may be possible once fully onboarded
Location : Noordkustlaan 16B 1702 Dilbeek

2025-34449 - Project Manager CAPEX - Life Sciences - M/F/X

Thu, 21 May 2026 22:03:16 Z

Category : OPERATIONS/CONSULTING
Contract : Permanent contract
Position description :
About the role We zijn op zoek naar een ervaren Project Manager Capex om onze klant te ondersteunen tijdens een scale up project. Deze rol is cruciaal voor de uitvoering van technische oplossingen. Je zorgt voor technische projectkwaliteit en zorgt ervoor dat het project binnen tijd en kosten blijft, dit volgens best practices. Key responsibilities Ondersteunen van interne & externe audits Aanvragen van vergunningen voor onderhoud/kalibratie/projecten Uitvoeren van FMEA en definiëren van onderhoudstype voor ieder activum; beoordelen van kriticiteit van apparatuur (HML) Engineering documenten opmaken/onderhouden/verifiëren Opstellen kostenramingen & Value Improvement Review Opstellen van project initiatiedocumenten (PBR, WBS, CBS, PSS) Identificeren van technische oplossingen Uitvoeren project HSE management & project veiligheidstops/beoordelingen Project uitvoeringsplan ontwikkelen Beheer project tekortkomingen en -afwijkingen Ontwikkel een kwalificatieplan Voer GMP-risicobeoordelingen uit DQ, IQ en OQ: maak protocollen op, voer deze uit en stel rapporten op Zorg voor technische probleemoplossing tijdens PQ en validatie

About you Diploma in engineering (Dipl. Ing. / M. Sc. / B. Sc.) of gelijkwaardig 5 jaar technische ervaring waarvan 2 in investeringsprojecten in de chemische/farmaceutische sector Leiderschapservaring in het beheer van externe middelen Bewezen projectmanagementvaardigheden, waaronder: contractmanagement en projectbeheersing HSE- en GxP/QA kennis en brede interdisciplinaire kennis Sterke beheersing van NL en ENG
Location : Noordkustlaan 16B 1702 Dilbeek