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Principal Scientist - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences, a contract research organisation with facilities in Montreal (Canada) and Gosselies (Belgium), offers analytical services to biopharmaceutical companies for the characterization of the human immune response in pre-clinical and clinical samples.

Caprion operates globally, with partners in North America, Europe and Asia, including large pharmaceutical companies and biotechs.

For its site in Gosselies and in the context of its growing immune monitoring service offering, Caprion is looking for a (m/f) :

Principal Scientist

Responsibilities :

Reporting to the Director of Scientific Operations and working closely with the laboratory personnel, the Principal Scientist will work within a team focusing on the characterization of the cellular and humoral immune response, using various types of assays such as flow cytometry (phenotypic, ICS, etc) ELISPOT, ELISA, Luminex and viral neutralization tests.

Responsibilities include:

  • Overseeing experimental design of flow cytometry, ELISPOT and antibody-based assays through generation of study-specific workplans and supporting documentation
  • Acting as a key resource to provide guidance and support in root cause analysis and impact assessment
  • Overall conduct of studies in different immune-therapeutic areas, acting as primary contact to the client for communication of study progress
  • Data interpretation, report generation and presentation of results to clients
Profile :

The applicant must hold a doctorate degree in life science, with strong knowledge of immunology, with post-doctoral experience (or equivalent) and have a deep expertise of flow cytometry analysis. The applicant must also have a minimum of two years of experience in the industry.

The applicant must :

  • Be proficient with analysis software such as FlowJo, Pestle, Spice, Prism and Excel and be able to perform complex analysis of flow cytometry data such as Boolean analysis.
  • Demonstrate excellent communication and organisational skills.
  • Be abreast of latest immune monitoring methodologies
  • Have an excellent knowledge and understanding of GCLP regulations and other regulatory guidelines sufficient to carry out GCLP studies.
  • Be willing to work in a Quality environment (ISO17025, GCLP, GMP) and apply good documentation practices (GDP).
  • Be fluent in English (written & spoken) and able to functionally communicate in French.
Offer :
  • Full time permanent contract.
  • Diversified tasks and responsibilities and interesting projects.
  • A professional, dynamic and stimulating work environment.
  • Development opportunities.
  • A competitive salary package including benefits, adapted to your experience and the context.

PLC and safety instrumented systems engineer - Oil industry - Antwerpen

As a global energy leader, Total is the fourth oil and gas company worldwide and a major player in low-carbon energies.

The Group operates in 130 countries and employs 98,000 people. Total explores for, produces, transforms, markets and distributes energy in a variety of forms, to serve the end customer.

Total’s strategy is to become the responsible energy major, providing affordable, reliable and clean energy to as many people as possible.

In order to strengthen the team in Antwerpen, we are actively looking for a (m/f) :

PLC and safety instrumented systems engineer

Responibilities :
  • Develop and realize soft- and hardware modifications on safety PLCs, non-safety PLCs, machine monitoring systems, industrial networks and SIS.
  • Follow up and support the exploitation and maintenance works on PLCs, monitoring systems and industrial networks, including analysis of failures.
  • Provide technical and general support to other departments on PLC systems, monitoring systems and SIS competence.
  • Update periodically the long term capital investment plan, according life cycle of systems, to prevent obsoleteness.
  • Develop projects up to +/- 500 k€ , including coordination of engineering phases, procurement of materials and services, coordination of project works, start-up, commissioning and training.
  • Participate in large multidisciplinary projects, supporting development and realization of PLC aspects.
  • Manage SIS technical data, including validation of safety test instructions and calculated SIL levels.
  • Follow up support and spare parts contracts with third parties.
  • Update and develop technical procedures.
  • Take an active role in the international networks of Total.
  • You are an engineer, or equivalent based on experience.
  • You have expertise in:
    • Classic instrumentation in a petrochemical environment.
    • Development and troubleshouting of various PLC and monitoring systems (preferentially: Honeywell FSC / Safety Manager, Hima Himatrix / Hiquad, Schneider Modicon, Bently Nevada).
    • Development and calculation of SIS (IEC61508, IEC61511).
  • You are fluent in both Dutch and English.
  • You demonstrate a high level of self-discipline, and have a high standard on quality and safety.
  • You have a pragmatic and analytical approach.
  • You are well organized and stress resilient.
  • You are a good communicator and a team player, and can also work independently in a complex and fast changing environment.
  • The opportunity to join an innovative and globally renowned industrial company.
  • Development opportunities and a structured evolution plan.
  • Professional and stimulating challenges.
  • A competitive salary package, in line with your experience.

Product Manager - Medical Device - Liège

Founded in 2016, Oncoradiomics is an innovative and ambitious start-up established in Liège. Oncoradiomics‘s strategic goal is to « revolutionize precision medicine”, by applying advanced artificial intelligence to clinical imaging.

Oncoradiomics focuses on tailoring cancer care to the clinical, imaging, biological and genetic characteristics of an individual patient so that the best outcome can be achieved.

Oncoradiomics holds several international grants and patents and is continuously developing and connecting with leading industrial and academic players to advance healthcare and the life sciences.

For the expansion of the team in Liège, we are looking for a (m/f):

Product Manager


As a Product Manager, you manage the off the shelf product portfolio and their associated Services & Support packages. The portfolio includes the Research ToolBox, the Discovery ToolBox (new) and the Clinical Solution.

You prioritize the launch of the Discovery ToolBox, targeting the top 50 to 300 clinics in the world. These clinics have a lot of patient images available and have not yet applied radiomics to these data. Their research arm is now ready to apply radiomics and try to discover new markers/signatures. The Discovery ToolBox needs to be an easy to use (GUI), integrated and rather automated tool, going beyond the basic radiomics feature extractor and including autocountouring, machine learning & DiCom viewer.

Your main responsibilities are:

  • You lead strategic thinking, stakeholder value proposition and business justification dialogue to choose the right road-map delivery goals for the portfolio. The whole product concept needs to be considered, i.e. also including Services, Support, Installation, …
  • You provide key inputs into the contractual set up with the customers and the clinical partners.
  • You define the product vision, road-map and innovation plans for the product portfolio and translate that into clear product specifications for the development teams in such a way that in short, mid and long term a sound business result can be achieved.
  • You manage and prioritize the portfolio backlogs using inputs from sales, customers and key opinion leaders.
  • In close collaboration with development, quality, scientific, customer support and with external experts, you follow the business during the life-cycle of the product and take corrective actions when needed, in order to generate the maximum profit contribution during the whole life cycle.
  • Master’s degree in Business, Biomedical Engineering or equivalent through experience.
  • Min. 3 to 5 years of experience in a product management position with technical products. Experience in medical imaging software and/or devices is a plus.
  • Agile/Scrum Master certification are an asset.
  • Results and customer oriented, rigorous, autonomous and flexible.
  • Analytical, organized, team player, open-minded with a start-up mind-set.
  • Fluent in English and in French. The command of any other language is an asset.
  • Strong oral and written communication.
  • Willing to travel for short periods up to 10% of your time.
  • A challenging and diversified position within a high-potential innovative start-up company.
  • To work in a dynamic, respectful and professional
  • International exposure, with learning and development opportunities.
  • An attractive compensation package in line with the position responsibilities and your ex

Head of RA - Bio-Pharma/Biotech - Liège

ASIT Biotech is a Belgian clinical-stage biotech company focused on the development of breakthrough immunotherapy products for the treatment of allergies.

Thanks to its innovative technology platform, ASIT Biotech currently holds a leading and unique position on the market. This innovation results in a short treatment, expected to improve patient compliance and quality of life. ASIT Biotech’s product pipeline targets to significantly expand the current immunotherapy market. For more information about the company, please vist

With a headcount of 25 staff members, ASIT Biotech is located in Liège, Belgium. In order to support its high-potential developments, we are looking for a (m/f):

Head of RA


As a Head of RA, you lead and drive the execution of ASIT global regulatory and quality assurance strategy. Reporting to the CEO, you are responsible for regulatory affairs, quality assurance, and compliance activities across the company. You define and implement the quality and regulatory policies in line with applicable directives, guidelines and legal requirements.

Your main responsibilities are as follows:

  • Develop, propose and implement the company regulatory & quality strategy.
  • Manage regulatory documents submissions for clinical studies, and product approvals.
  • Implement an efficient quality system and a continuous improvement culture within the company.
  • Interact with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, and follow-up of
  • Support and advise project teams on regulatory and quality issues.
  • Provide technical review of data and reports for regulatory submissions.
  • Draft product labelling, instruction leaflets and packaging.
  • Participate in internal/external audits, inspections and provide post-inspection
  • Write and update SOP, work instructions, and policies.
  • Master or PhD in life sciences or equivalent through experience.
  • 10 years experience in a RA and/or a QA management position in the Biotech/Pharma sector.
  • Track record in developing quality systems from EU/US clinical developments to product approval.
  • Thorough knowledge of ICH guidelines, GxP and related regulatory guidances.
  • Proven track record of building strong relationships with internal and external stakeholders.
  • Ability to maintain multiple projects and meet timelines, including change management skills.
  • Client-centered and solution-oriented, with hands-on and pragmatic mindset.
  • Excellent leadership, communication and interpersonal skills.
  • Familiar with MS Office solutions.
  • Fluency in English.
  • A challenging leading position within a stimulating and dynamic work environment.
  • A variety of interesting contacts with international exposure.
  • The opportunity to have direct impact on the results of a high-potential biotech company.
  • An attractive compensation package in line with the position responsibilities and your experience.

Responsable de Production - Belgian Brewery - Péruwelz

La Brasserie Caulier est une entreprise familiale de la région de Tournai, située à Péruwelz. La brasserie produit ses propres bières depuis près de 20 ans et jouit d’une excellente réputation dans le secteur.

L’équipe actuelle, composée de 17 passionnés, brasse des bières 100% naturelles, appliquant des méthodes de fabrication artisanales. La brasserie connaît une croissance importante depuis quelques années et vient d’entamer un vaste plan d’investissement qui lui permettra de doubler sa capacité de production.

Afin de soutenir la croissance de la Brasserie Caulier, nous sommes à la recherche d’un (h/f) :

Responsable de Production

Responsabilités :

Rattaché au Directeur Général et Membre du Comité de Direction, vous êtes responsable de l’ensemble de la production de la Brasserie dans un contexte de grande croissance.

Vos responsabilités principales sont de :

  • Organiser et optimiser l’ensemble de la production de la Brasserie dans le respect des coûts, des délais et de la qualité (achats, process, ressources humaines) ;
  • Proposer, planifier et mettre en œuvre les investissements dans l’outil de production de manière à augmenter tant la capacité que l’efficacité ;
  • Gérer une équipe de 15 personnes (contre-maîtres et opérateurs de production) et recruter les équipes nécessaires aux objectifs élevés de croissance ;
  • Piloter le volet « production » de l’ERP en impliquant les équipes, et en faisant ressortir des données utiles au management ;
  • Remplir et communiquer l’ensemble des documents légaux relatifs à la production, dans le respect de la réglementation en vigueur ;
  • Mettre en place, analyser, et communiquer des indicateurs de performances à la direction et aux équipes de production.
Profil :
  • Vous êtes Ingénieur Civil, Ingénieur Agronome ou équivalent ;
  • Vous avez au moins 5 années d’expérience, dont au moins 3 années dans une fonction managériale dans l’industrie agroalimentaire ;
  • Vous démontrez une passion pour la gestion d’entreprise et le monde brassicole ;
  • Vous êtes un réel chef d’équipe et leader, vous savez manager, déléguer, motiver, faire grandir vos collaborateurs ;
  • Une bonne connaissance de l’utilisation d’un ERP constitue un atout ;
  • Une expérience de conduite de projets de développement dans le monde brassicole serait un atout supplémentaire ;
  • Vous disposez de très grandes compétences analytiques et organisationnelles ;
  • Vous êtes reconnu pour votre sens relationnel, vous êtes pragmatique et orienté solutions ;
  • Vous êtes reconnu pour votre rigueur, votre autonomie, votre sens de la diplomatie et votre capacité à travailler par projet.
Offre :
  • Une fonction diversifiée comprenant de nombreuses responsabilités ;
  • L’opportunité de rejoindre une entreprise professionnelle, familiale et conviviale, et de contribuer à sa forte croissance ;
  • Des possibilités de formation, de développement et, éventuellement, de coaching ;
  • Un contrat à temps plein et à durée indéterminée, assorti d’un package salarial adapté à votre profil et à votre niveau d’expérience.

Technico-Commercial Junior - Industry - Forest

Située à Forest et composée d’une vingtaine de personnes, Dumont Instruments est une entreprise familiale qui existe depuis près de 40 ans. La société est active dans la conception, la production et la commercialisation de fraises de haute précision pour outils rotatifs.

Sa clientèle se compte principalement dans le secteur dentaire en France et en Belgique (dentistes, laboratoires de prothèses dentaires, etc.), mais également parmi certaines industries en Europe et dans le monde. Pour plus d’informations, veuillez visiter

Pour accompagner le Directeur Industrie dans le développement commercial de la société, nous recherchons activement un (m/f) :

Technico-Commercial Junior

Responsabilités :

En tant que Technico-Commercial Junior, vous participez au développement commercial de la société. Rapportant au Directeur Industrie, vous l’accompagnez dans ses différentes missions.

Vos principales tâches sont les suivantes :

  • Veiller au suivi administratif et logistique des différents contrats (ex : facturation des clients, réception des commandes, etc.).
  • Assurer la coordination de la production du pôle industrie.
  • Traduire les besoins techniques des clients via un programme de design industriel (ex : AutoCad).
  • Proposer des solutions techniques et commerciales adaptées aux besoins des clients.
  • Développer une relation de confiance avec les clients et les fournisseurs afin d’assurer une bonne collaboration sur le long terme.
  • Prospecter de nouveaux clients et augmenter la visibilité de Dumont Instruments.
  • Rapporter de manière régulière et structurée l’évolution des démarches réalisées.
Profil :
  • Vous êtes fraichement diplômé(e) d’un Bachelier en mécanique ou électromécanique.
  • Vous disposez idéalement d’une bonne connaissance d’un programme de design industriel tel que AutoCad.
  • Vous êtes orienté(e) clientèle, résultats et solutions, et doté(e) d’un bon relationnel.
  • Vous êtes passionné(e) par la technique liée à l’usinage de précision, curieux(se) et avez l’envie d’apprendre.
  • Vous êtes analytique, organisé(e), autonome et rigoureux(se).
  • Vous communiquez aisément en français et en anglais (oral et écrit). La connaissance du Néerlandais est un atout.
  • Vous êtes disposé(e) à vous déplacer environ 25% de votre temps sur le territoire confié (prioritairement en Belgique, France et Luxembourg).
Offre :
  • Une fonction commerciale stimulante dans une entreprise conviviale et dynamique.
  • L’opportunité de commercialiser des produits belges dont la qualité est internationalement reconnue.
  • Des contacts diversifiés sur l’ensemble du territoire confié.
  • Un parcours de formation dès votre entrée en fonction et tout au long de votre carrière au sein de Dumont Instruments.
  • Un contrat à durée indéterminée à temps plein.
  • Un salaire attractif assorti d’avantages extra-légaux, en phase avec votre expérience.

Chief Operating Officer - Biotechnology - Brabant wallon

A-MANSIA is a biotech company focusing on microbiome therapeutics addressing human health issues like obesity and related disorders. The mission of A-MANSIA is to provide innovative solutions based on Microbiome Therapeutics.

Under the implementation plan in the Walloon Brabant province, its future development and reinforced by a 21 million euros fundraising success, A-MANSIA is looking for a dynamic and enthusiastic person to strengthen the team. For more information about the company and the technology, please contact us via

A-MANSIA offers a French, Dutch and English-speaking environment, culturally diversified and located in the heart of Europe, in Belgium, a few hours from European Capitals. To strengthen the team in Mont-Saint-Guibert, we’re looking for an (m/f):

Chief Operating Officer

Main responsibilities:

Reporting directly to the CEO and as part of the executive committee, you are in charge of the whole operations management for the fermentation process starting from the sourcing of raw materials to the commercialisation of finished products. You are the point of contact with the CMO(s) in charge of the outsourced manufacturing of microbial products.

Your main tasks are:

  • Lead production projects and product launch on the market: sourcing of raw materials with the CMO, logistic, galenic development & packaging.
  • Coordinate with R&D and marketing departments to oversee the whole operation process.
  • Coordinate the whole outsourced production and supply chain.
  • Be part of the COMEX and report to Board of Directors on the strategic development of operations.
  • Define specifications, negotiate contracts and manage the collaboration with CMOs and third parties.
  • Ensure raw materials compliance and control outsourced performances.
  • Control and lead the Cog’s at the product launch and on a long-term basis.
  • Manage the internal supply chain team.
  • You hold a Ph.D. or you are engineer in Nutrition or Life Sciences, or equivalent through experience.
  • You have at least 10 years of industrial experience in production management related to the production of probiotics/food complements.
  • You have experience in and knowledge of fermentation processes.
  • You have hands on experience in or knowledge of CMO and third parties management.
  • You show strong leadership skills combined with a strategic and hands-on approach.
  • You are skilled in project management related to food complements launch on the market.
  • You take advantages of an extended network in the industry.
  • You are rigorous, flexible, hands-on, independent, dynamic and pro-active.
  • You are fluent in English. The command of French and/or Dutch is an asset.
Offer :
  • A diversified executive position within a high-potential start-up company.
  • A key position for the development of the company.
  • The opportunity to join a human sized, dynamic and professional environment.
  • A permanent employment contract.
  • An attractive compensation package in line with your experience.

Responsable des Opérations - Industrial Services - Binche

Tivolux Pro/Atome Alu est spécialisée en fabrication de châssis et portes en PVC et en aluminium à destination des professionnels. Tivolux Pro/Atome Alu s’impose ensemble comme un des leaders wallons dans ce domaine depuis plus de 10 ans.

Située à proximité de Binche, Tivalux Pro/Atome Alu est composée d’une quarantaine de personnes dont trente dévouées à la production, elle dispose également de son propre parc de machines. Pour plus d’information sur l’entreprise, veuillez consulter

Afin de renforcer l’équipe de Tivolux Pro/Atome Alu, nous sommes à la recherche d’un (m/f) :

Responsable des Opérations

Responsabilités :

En tant que Responsable des Opérations, vous dirigez la production alliant les activités de fabrication, de planification, d’achat et de maintenance. Vous implémentez progressivement une vision et une culture de travail industrielle. En outre, vous promouvez la qualité, la sécurité et l’amélioration continue.

Vos principales responsabilités sont les suivantes:

  • Coordonner et optimiser le fonctionnement de la production.
  • Diriger, motiver et développer les collaborateurs de l’équipe.
  • Mettre en œuvre la stratégie de l’entreprise au sein des opérations et veiller à l’amélioration continue.
  • Garantir l’application des règles de sécurité, des normes de qualité et du règlement intérieur.
  • Organiser et être responsable de l’ensemble des moyens techniques.
  • Rapporter de manière structurée, rigoureuse et adaptée les résultats des activités.
Profil :
  • Vous êtes titulaire d’un diplôme d’ingénieur ou équivalent par expérience.
  • Vous disposez d’environs 10 années d’expérience dans une fonction comparable au sein d’un environnement de production industrielle.
  • Vous communiquez efficacement, avec assertivité, et possédez une certaine aisance relationnelle.
  • Vous êtes à l’écoute et faite preuve d’empathie envers vos collaborateurs.
  • Vous faites preuve de leadership, et démontrez des compétences en change management.
  • Vous parlez couramment Français. La connaissance de l’Anglais est un atout.
  • Vous vous déplacez ponctuellement chez les fournisseurs et/ou clients.
Offre :
  • Une fonction diversifiée en étant acteur du changement d’une industrie reconnue pour la qualité de ses produits.
  • Des défis professionnels et humains stimulants et enrichissants.
  • L’opportunité d’évoluer rapidement et d’acquérir de nouvelles responsabilités.
  • Un salaire attractif reprenant des avantages extra-légaux en phase avec votre expérience.

Sales Executive - Medical Device - Liège

Founded in 2016, Oncoradiomics is an innovative and ambitious start-up company based in Liège. Oncoradiomics’ strategic goal is to “revolutionize precision medicine”, by applying advanced artificial intelligence to clinical imaging.

Oncoradiomics focuses on tailoring cancer care to the clinical, imaging, biological and genetic characteristics of an individual patient so that the best outcome can be achieved.

Oncoradiomics holds several international grants and patents and is continuously developing and connecting with leading industrial and academic players to advance healthcare and the life sciences.

In order to support the further development and growth of the company, we are looking for a (m/f):

Sales Executive

Responsibilities :

As a Sales Executive, you are accountable for sales results. You are responsible for developing strategic accounts in the pharma sector, executing the strategic account plan. You develop existing client relationship while prospecting new customers.

Your main responsibilities are :

  • You develop strategic account plan in order to meet the sales objectives.
  • You own the 360 relationship and business for each named account.
  • You team-up with the right people to execute the account plans.
  • You generate leads through active prospection, sales and marketing campaigns.
  • You promote and sell key offers through with the support of the scientific and technology teams.
  • You detect, select, prioritize and manage major opportunities to focus on.
  • You drumbeat the relationship with the client : contract, purchase order and cash collection.
  • You ensure client satisfaction and client intimacy, doing client power/influence mapping.
  • You identify and summarize client needs in terms of resources to power the strategic account plans.
Profile :
  • You hold a Master’s degree in Business or in Science.
  • You have at least 5 years of experience as an Account Manager in the pharma sector.
  • You are a self-starter, an entrepreneur minded person with a strong business drive and acumen.
  • You have a « can do » mentality and are energized by complex & demanding commercial environments, including contract negotiation.
  • You can easily build relationships and team play.
  • Structured and straight-forward, you are passionate for applying technology, especially in life science.
  • You demonstrate strong interpersonal skills and business management skills.
  • You are fluent in English and French. Any other European language is an asset.
  • You are ready to travel, up to 40% of your time (short-trips).
Offer :
  • A challenging and diversified position within a high-potential innovative start-up company.
  • The unique opportunity to help shape the company’s success to the international scale.
  • A young, leading edge, and multicultural environment.
  • An attractive salary package in line with the position responsibilities and your experience.

Program Management Officer - Biotechnology - Gosselies

Located in Gosselies (Belgium), MaSTherCell is a service company (CDMO) in biotechnology. MaSTherCell is specialized in production outsourcing, process development and quality management (QA/QC/QP) for cell therapy.

With around 140 employees, MaSTherCell supports its customers (big pharma, biotech, etc.) in the development and production of innovative medicines. MaSTherCell actively contributes to improving the quality of life and health of many patients. For more information, please visit

To support MaSTherCell in its strong growth, we are actively looking for a (m/f):

Program Management Officer


Reporting to the Executive committee, you assist them in selecting and planning strategic internal projects/programs (including new sites integration), and in reporting on their progress.

Your main responsibilities are:

  • You implement project management tools, project control processes, procedures and policies.
  • You monitor and control the internal program/project throughout their entire lifecycle.
  • You select program/project and you argue program/project closedown if necessary.
  • You assess the relative priority of internal projects and programs.
  • You set up performance reporting and program/project governance for customer and internal projects.
  • You lead the project financial tracking with the business controller.
  • You provide support to project teams and task planning.
  • You report your work on a regular basis.
  • Master’s degree or equivalent through experience.
  • Minimum 5 years experience in a project management officer position.
  • A project management professional certification is an asset.
  • Strong communication skills together with hands-on and pragmatic mind-set.
  • Very good organizational, analytical and problem-solving skills.
  • Highly collaborative, self-motivated and team-oriented individual in a company setting.
  • Good oral and written communication skills in English. Any other language is a plus.
  • Computer skills:  Microsoft office, Digital document management system and Project management IT tools.
  • A challenging and diversified position within a high-potential innovative biotech company.
  • To work in a human size, dynamic, respectful and professional environment.
  • A variety of interesting contacts with international exposure.
  • An attractive compensation package in line with the position responsibilities and your experience.