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R&D Engineer – Catheter - Medical Device - Awans (Liège)

Founded in 2009, CryoTherapeutics is an early stage European innovative company that is now establishing its operations in Liège (Awans). The company is in the process of developing a novel catheter system to treat atherosclerotic plaque that causes heart attacks by delivering cryoenergy to the coronary arteries. For additional information about the company, please visit http://www.cryotherapeutics.com/

CryoTherapeutics aims to develop and market the novel cryoenergy therapy initially for patients who have suffered a heart attack, and in the longer term also for patients identified as being at future risk of heart attack. CryoTherapeutics recently raised 7M€ in its latest round of financing and will use these funds to continue development of this technology with the aim of starting clinical studies later this year.

In order to support the expansion of the team in Awans, we are looking for a (m/f):

R&D Engineer – Catheter

Responsibilities:

As a R&D Engineer – Catheter, the candidate will lead and take care of designing, developing and testing next-generation catheter delivery systems from concept to human use. Reporting to the CTO you play a key role in the R&D/innovation activities.

The position’s main responsibilities are:

  • Conceptualize, design and develop innovative interventional catheters, including design requirements, prototype developments, pre-clinical and clinical assessments, and industrialization.
  • Support the design of the next generation catheter components, in collaboration with Quality.
  • Support the development of new test methods, tooling and equipment procurement, and executing long term testing for catheters.
  • Collaborate with colleagues and physicians in both pre-clinical and clinical developments in order to evaluate technology and to have a better understanding of cardiovascular anatomy.
  • Work with team members and external partners to deliver project’s technical objectives.
  • Report results and work evolution on a regular basis to the top management.
  • Establish timelines and ensures adherence to timely execution
  • Develop appropriate test methods for product evaluations, writes and executes test protocols and test reports required per GMP and regulatory submissions
Profile:
  • Mechanical or Biomedical Engineering Master’s degree.
  • First experience in design, development and industrialization within medical device companies.
  • Experience with catheters is a strong asset.
  • Relevant technical expertise on extrusion, braiding, molding, and bonding processes.
  • Experience in materials (plastics, adhesives and associated processes), and mechanical (small part) design is desired.
  • Experienced in medical device regulatory requirements, QMS and design control processes is an asset.
  • Proven record of working with and managing vendors for product and process specification and testing.
  • Strong innovation and 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.
  • Excellent oral and written communication skills in English. Any other language is a plus.
  • Up to 25% travel may be required.
Offer:
  • A challenging position with a high potential innovative medical device company.
  • To work in a human-sized, collaborative and respectful environment
  • A variety of interesting contacts with international exposure.
  • An attractive compensation package in line with the position’s responsibilities and your experience.

Principal Scientist - CRO, R&D Medical & Science - Gosselies

Caprion Biosciences, an international contract research organisation based in Montreal (Canada) offers analytical services to biopharmaceutical companies for the characterization of the human immune response in pre-clinical and clinical studies.

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

In the context of its growing immune monitoring service offering, Caprion is looking to hire a Principal Scientist for its flow cytometry and serology platforms, for its site in Gosselies, Belgium.

Principal Scientist

Function :

Reporting to the Associate Director, 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 (phenotyping, receptor occupancy, phosflow, ICS, etc) ELISPOT, ELISA, 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;
  • Overall conduct of studies in different immune-therapeutic areas, acting as primary contact to the client for communication of study progress;
  • Ensures that timelines and milestones are met and are in line with company objectives;
  • Data interpretation, report generation and presentation of results to clients.
Profile of the applicant:

The applicant must hold a doctorate degree in life science, with strong knowledge of immunology, and preferably with post-doctoral experience (or equivalent).  Experience in the industry is a strong asset.

The applicant must :

  • 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 regulated studies and apply good documentation practices (GDP);
  • Experience in assay validation is an asset;
  • Be proficient with analysis software;
  • Be fluent in English (written & spoken) and able to functionally communicate in French;
  • Be willing to travel mainly within Europe and occasionally to other continents.
Offer :
  • Full time permanent contract, with possibility of rapid start.
  • Diversified tasks and responsibilities.
  • A professional, dynamic and stimulating work environment.
  • Training and development opportunities.
  • A competitive salary package including benefits, adapted to your experience and the context.

Sales Manager – Industrie - Oil industry - Verviers

LubriGroup est une belle entreprise familiale située à Verviers. Composée d’une quinzaine de personnes, l’entreprise comprend 3 entités : Lubrix, active dans la lubrification industrielle ; Lubri-Asept, active dans la désinfection et le nettoyage ; et Activ’Aqua qui propose des solutions et des produits pour piscines.

Lubrix formule, produit et commercialise des lubrifiants et des huiles de coupe pour le secteur industriel, plus spécifiquement pour les machines-outils, d’usinage et de laminage.

Afin de soutenir la croissance de Lubrix, nous sommes activement à la recherche d’un(e) :

Sales Manager

Responsabilités :

En tant que Sales Manager, vous maintenez et développez les relations avec les clients existants et assurez la prospection et l’identification de nouvelles opportunités commerciales. Rapportant au Responsable Commercial, vous assurez le développement du chiffre d’affaires pour les produits de lubrification pour l’industrie.

Vos principales responsabilités sont les suivantes :

  • Développer et fidéliser un portefeuille clients existant.
  • Prospecter activement sur le terrain de nouveaux clients.
  • Apporter un support et une expertise technique aux clients.
  • Maintenir des relations positives avec les clients et veiller à leur satisfaction.
  • Réaliser les objectifs de vente et contribuer à la croissance de la société.
  • Mener vos démarches dans le respect des objectifs de qualité, coûts et délais.
  • Assurer un reporting régulier et efficace de votre activité.
Profil :
  • Vous avez une première expérience commerciale réussie, idéalement en milieu industriel.
  • Vous possédez un diplôme d’études supérieures ou équivalent par expérience.
  • Vous avez des affinités avec la technique et le milieu industriel.
  • Vous avez une très bonne maîtrise du français et une bonne connaissance de l’anglais.
  • Vous avez d’excellentes compétences relationnelles et commerciales.
  • Vous êtes autonome et avez le sens des responsabilités.
  • Vous êtes organisé(e), orienté(e) clientèle et solutions.
  • Vous êtes disposé(e) à vous déplacer régulièrement en Belgique francophone.
Offre:
  • Une fonction commerciale stimulante et diversifiée au sein d’une PME en croissance.
  • L’opportunité de rejoindre un environnement à taille humaine, dynamique et professionnel.
  • Des contacts diversifiés sur l’ensemble du territoire confié.
  • Un contrat à temps plein à durée indéterminée (CDI).

Global Head of Regulatory Affairs - Bio-Pharma/Biotech, Biotechnology - Gosselies

iTeos Therapeutics is a privately-held, clinical-stage biopharmaceutical company dedicated to extending and improving the lives of cancer patients by designing and developing next generation immunotherapies. iTeos Therapeutics is advancing its two main programs into a phase I/II clinical stage. The first program is an insurmountable and non-brain penetrant adenosine A2A receptor antagonist. The second program is a human ADCC-enabling anti-TIGIT antibody.

Based in Gosselies, Belgium and Cambridge, MA, iTeos Therapeutics was founded out of the Ludwig Institute for Cancer Research (LICR) and the de Duve Institute (UCLouvain) in 2011. In March 2020, the Company completed a $125 million Series B2 financing led by 6 main US Venture Capitalists. All previous investors including Fund +, VIVES II and SRIW, as well as SFPI, also participated in this funding round. For more information, please visit www.iteostherapeutics.com.

iTeos Therapeutics is now a world-class actor in the sector. To carry on its growth and reinforce its team, iTeos Therapeutics is looking for a (m/f) :

Global Head of Regulatory Affairs

The Global Head of Regulatory Affairs will be a key member of iTeos Therapeutics’ Leadership Team and be responsible for developing iTeos Therapeutics’ global regulatory strategy, represent iTeos in regulatory interactions and ensure execution of regulatory requirements and provide input into internal quality systems. This role requires expert interpretation of requirements relating to the development and licensing of cancer therapeutics and communication to cross-functional teams to create innovative regulatory strategies for targeted small molecules and biologics to treat cancer. This position will report to the Chief Medical Officer and will have extensive interface with the senior management team.

Main responsibilities:
  • Responsible for developing innovative global regulatory strategies and working with the cross-functional project team on execution.
  • Leads interactions with global regulatory agencies.
  • Represents regulatory affairs in the leadership team and on cross-functional project teams to provide regulatory guidance and education through the interpretation of regulations, policies, procedures, guidelines, and compliance requirements.
  • Provides oversight for regulatory staff (whether at CRO or internally) and assesses and makes recommendations on staffing requirements.
  • Develops and manages regulatory submissions and related supplements and amendments with the support of a CRO.
  • Responsible for developing and maintaining regulatory strategy documents.
  • Interacts directly with health authorities and maintains excellent relationship with regulatory personnel.
  • Works with the team to integrate biomarker/companion diagnostic strategies into the development of assigned programs.
  • Educates company on regulatory requirements and evolving trends and disseminates regulatory policy and intelligence relevant to the business.
  • Provides regulatory due diligence assessments of new business opportunities.
Profile:
  • Advanced degree in a scientific or health-related field
  • Seasoned professional with at least 10 years of regulatory affairs experience in the biopharmaceutical industry
  • Exceptional communication and presentation skills to articulate complex regulatory strategy and decision-making both internally and externally
  • Experience and comfort with pushing the boundaries and asking challenging questions both of the internal team and of the regulatory authorities.
  • Experience in providing strategic advice on integrated regulatory development plans and executing regulatory strategy for cancer therapeutics.
  • In-depth working knowledge of regulations, guidance, policies, and procedures pertinent to drug and biologics development and operational knowledge of IND/CTA and NDA/BLA/MAA submissions.
  • Experience with development of biomarkers and IVD companion diagnostics devices preferred.
  • Exceptional writing skills with experience in drafting and submitting timely drug and biologic applications to health authorities.
  • Track record of building an excellent relationship with the FDA, EMA and other regulatory agencies.
  • Quality mindset.

LEADERSHIP CHARACTERISTICS :

  • Entrepreneurial, resourceful, energetic, self-starter
  • Approaches challenges with creativity and pragmatism
  • Ability to engage team to achieve goals without direct authority
Offer:
  • A stimulating scientific position within a high-potential innovative biotech company.
  • The opportunity to work in a science-driven, dynamic, human‐sized, respectful and professional environment.
  • A challenging scientific and business growth in which you get to bring your knowledge and skills.
  • Varied contacts inside the company, the biotech/pharma sector and the scientific world.
  • A long-term contract and an attractive salary package in line with the position responsibilities and your experience.

Research Technician – In Vivo Pharmacology - Bio-Pharma/Biotech, Biotechnology - Gosselies

iTeos Therapeutics is a privately-held, clinical-stage biopharmaceutical company dedicated to extending and improving the lives of cancer patients by designing and developing next generation immunotherapies.

Based in Gosselies, Belgium and Cambridge, MA, iTeos Therapeutics was founded out of the Ludwig Institute for Cancer Research (LICR) and the de Duve Institute (UCLouvain) in 2011. In March 2020, the Company completed a $125 million Series B2 financing. For more information, please visit www.iteostherapeutics.com.

iTeos Therapeutics is now a world-class actor in the sector. To carry on its growth and reinforce its team, iTeos Therapeutics is looking for an (m/f) :

Research Technician – In Vivo Pharmacology

Keys responsibilities:

As a Research Technician, you perform in vivo assays to discover and to validate small molecules and biologics for the development of innovative cancer immunotherapies. Your main responsibilities are as follows :

  • Perform experimental in vivo models of cancer, including compound dosage and endpoint assessment, according to Standard Operating Procedures.
  • Perform pharmacokinetic and pharmacodynamics studies.
  • Systematically compile data and report in Excel and in Prism files.
  • Collaborate with other project stakeholders and discuss assays results with them.

This function requires occasional presence on Saturdays or Sundays (more or less once a month). The function may from time to time require starting work before 8am or ending the day between 5-7pm.

Profile:
  • Bachelor in Life Sciences, Pharmacology, Biochemistry or closely related field.
  • FELASA B/C certified.
  • Experience in in vivo studies is a must.
  • Previous experience in Culture of cell lines for in-vivo studies and/or standard lab techniques (ELISA, qPCR, flow cytometry, etc.) is a plus.
  • Previous experience in the biotech/pharma industry or in a similar academic position is an advantage.
  • Knowledge of Microsoft Office. Knowledge of Prism is a plus.
  • Good communication skills in French and English.
  • Rigorous, detail-oriented, organized, autonomous, committed and flexible.
  • Strong team spirit and excellent interpersonal skills.
Offer:
  • A stimulating scientific position within a high-potential innovative biotech company.
  • The opportunity to work in a science-driven, dynamic, human‐sized, respectful and professional environment.
  • A challenging scientific and business growth in which you get to bring your knowledge and skills.
  • Varied contacts inside the company, the biotech/pharma sector and the scientific world.
  • A long-term contract and an attractive salary package in line with the position responsibilities and your experience.

(Sr.) Scientist – Immuno-Oncology Target Validation - Bio-Pharma/Biotech - Gosselies

iTeos Therapeutics is a publicly held (NASDAQ: ITOS), clinical-stage biopharmaceutical company dedicated to extending and improving the lives of cancer patients by designing and developing next generation immunotherapies.

Based in Gosselies, Belgium and Cambridge, MA, iTeos Therapeutics was founded out of the Ludwig Institute for Cancer Research (LICR) and the de Duve Institute (UCLouvain) in 2011. In March 2020, the company completed a $125 million Series B2 financing, and in July 2020, completed its IPO raising over $200million of proceeds.

This additional capital will allow iTeos Therapeutics to continue to develop its clinical pipeline and maintain its investments in its discovery research team to leverage fantastic science to improve the lives of cancer patients. For more information, please visit www.iteostherapeutics.com.

To strengthen the team in Gosselies, we are looking for a (m/f) :

(Sr.) Scientist – Immuno-Oncology Target Validation

 

Responsibilities :

Within the Preclinical Department, you will play a key role in the discovery, investigation and validation of new targets to expand the iTeos pipeline and help develop breakthrough cancer immunotherapies. You will generate robust in vitrodata packages on one or more Immuno-Oncology targets, helping to guide decision making and timely progression to development and clinical trials.

  • Lead the validation of new targets by providing key data all along the project development towards a preclinical program and later on, to the clinic.
  • Design, validate and carry experimental in vitro immunoassays using Standard Operating Procedures.
  • Develop new immunoassays that will help deepen the biological knowledge of the drug target and characterize the mode of action of biologic candidates.
  • Compile, summarize and critically analyze data in order to present them at project team meetings.
  • Show strong ownership by being up to date with the project literature and more broadly with the immune-oncology field.
  • Collaborate with external contacts, either with academic partners or with CRO’s.
Profile :
  • PhD and/or post-doc in (Tumour) Immunology.
  • Hands-on experience in the biotech/pharma industry would be valued and give you access to the Senior Scientist position.
  • Strong expertise in immunology techniques such as primary cell isolation, setting-up immune cell-based assays (e.g. in vitro stimulation of immune cells, suppression assays, antigen recall assays) and advanced flow cytometry.
  • Additional molecular cell biology/immunology techniques are assets.
  • Strong track record of scientific publications or productivity (posters, presentations, etc.).
  • Excellent command of English (oral and written).
  • Committed and detail-oriented, strong sense of time management and flexibility.
  • You are both autonomous and a team player with an inquisitive mindset and strong problem-solving skills.
  • You are very open-minded and have excellent interpersonal and communication skills.
Offer :
  • A stimulating position within a high-potential innovative biotech company.
  • The opportunity to work in a science-driven, dynamic, human‐sized, respectful and professional environment.
  • A challenging scientific and business growth in which you get to bring your knowledge and skills.
  • A permanent contract with an attractive salary package in line with the position responsibilities and your experience.

Quality Assurance and Regulatory Affairs Manager - Biotech, Biotechnology - Flémalle

Created in 2013, Wishbone is an innovative start-up located in Flemalle (Liege). Wishbone is engaged in the development of intraoral bone regeneration biomaterials. The company has launched its industrialization and production activities in a brand new production unit and has successfully reached ISO 13485 certification.

The goal of Wishbone is to develop superior bone graft substitute products with breakthrough technologies and innovative procedures, and thus improve patient well-being and contribute to a better environment. The company will launch its forst commercial product and several other innovative products are under development. For more information please visit: www.wishbone-biotech.com

To support this challenging development, we are looking for a (m/f):

Quality Assurance and Regulatory Affairs Manager

Responsibilities:

As a Quality Assurance and Regulatory Affairs Manager, you are responsible for managing the company Quality Management System and its related activities. You are also responsible for the Regulatory Affairs Management. You ensure the company and the products are compliant with the appropriate standards and regulations. You provide support in the Quality Management System maintenance and improvements. This includes the development of systems, policies/procedures and programs to ensure compliance with the EU and FDA regulations, ISO standards, and other international requirements.

You have a cross-functional role, directly manages a small team of QA/RA Associate and Product Specialist and interact with all departments and with the top management.

Your main responsibilities are :
  • Managing the Quality Management System according to the EU ISO 13485, the US FDA 21 CFR Part 820 and any other relevant regulatory requirements in accordance with the Quality Policy.
  • Ensuring that required processes of the Quality Management System (QMS) are documented, established, implemented and maintained.
  • Assuring that products have been supplied, manufactured, analyzed and released according to specifications and approved SOP’s and to appropriate standards and regulations.
  • Organizing and documenting the Management Review according to the company QMS. Recommending and driving improvement.
  • Performing supplier audits, internal and external audits and interacting with suppliers and customers to deal with non-conformities and drive continuous improvement.
  • Supporting activities for CE marking and FDA approval certification of products as well as maintaining the documentation up to date when changes to the product occur, dealing with notifications and amendments when required.
  • Managing materiovigilance activities including incident and post-market surveillance reporting.
  • Ensuring the promotion of awareness of applicable regulatory requirements and quality management system requirements throughout the organization.
  • Reporting to the management on the effectiveness of the Quality Management System and any need for improvement of the company organization.
Profile:
  • Scientific Master’s degree, or equivalent through experience.
  • At least 5 years of experience in QA management positions in the medical devices industry.
  • Strong understanding of regulations and guidelines governing medical devices (e.g. CFRs, ISO 13485, MDD, MDR).
  • Strong leadership, project management and communication skills together with hands-on and pragmatic mind-set.
  • Ability to work in a start-up environment where accuracy, accountability, quality, safety and timeliness are essential.
  • Highly collaborative, self-motivated and team-oriented individual in a company setting.
  • Excellent oral and written communication skills in French and English. 
Offer:
  • The opportunity to join an innovative medical device company, a fast-growing start-up environment where teamwork, results and patient care are very important.
  • A challenging and diversified position in a dynamic, young and nice
  • To work in a human size, respectful and professional environment.
  • An attractive compensation package in line with the position responsibilities and your experience.

IT Application Manager - Radio–Pharma - Fleurus

Situées à Fleurus (Belgique), l’IRE et sa filiale IRE ELiT sont des entreprises industrielles renommées et innovantes jouissant d’un potentiel de développement élevé.

Avec près de 250 collaborateurs, l’IRE est l’un des principaux producteurs mondiaux de radio-isotopes utilisés en médecine nucléaire à des fins de diagnostic et de thérapie. IRE ELiT est quant à elle active dans la production radio-pharmaceutique.

Plus concrètement, ces entreprises contribuent à sauver des millions de vies dans le monde chaque année. Sur les 5 dernières années, l’entreprise a renforcé son développement et jouit d’une croissance continue. Pour plus d’informations, veuillez consulter www.ire.eu

Pour assurer le bon développement de l’IRE, nous sommes activement à la recherche d’un (m/f) :

IT Application Manager

Responsabilités :

Rapportant au Directeur des Opérations, vous supervisez et maintenez à jour les applications software en mettant en œuvre les bonnes pratiques. Vous assurez l’efficience des systèmes d’application, en optimisant les coûts et en garantissant un haut niveau de satisfaction des utilisateurs.

Vos principales responsabilités sont les suivantes :

  • Évaluer les besoins et requis de l’entreprise en solutions applicatives.
  • Mener le déploiement d’un nouvel ERP et son développement à travers toute l’entreprise.
  • Coordonner et mener à bien la digitalisation de l’entreprise.
  • Gérer le cycle de vie des applications et veiller à l’adéquation de la partie hardware.
  • Superviser le design, le développement et le déploiement des systèmes IT critiques.
  • Assurer la veille technologique, développer et optimiser des solutions.
  • Supporter la résolution de problèmes liés aux applications.
  • Créer et améliorer des processus et protocoles pour l’usage des applications. S’assurer que les bonnes pratiques et les standards soient appliqués.
Profil :
  • Vous êtes titulaire d’un Master à orientation IT.
  • Vous disposez de 10 années d’expérience, idéalement dans le secteur industriel/manufacturing, dont 3 ans dans un rôle de leadership.
  • Vous avez une expérience dans le déploiement d’un ERP et en gestion de projets transversaux.
  • Vous êtes orienté(e) solutions et résultats, et faites preuve d’assertivité et de diplomatie.
  • Rigoureux/se, pragmatique et autonome, vous êtes doté(e) d’une forte capacité organisationnelle et relationnelle.
  • Vous êtes capable de mobiliser les équipes, challenger le statu quo et d’exercer une influence sur l’organisation.
  • Vous jouissez d’une très bonne connaissance du français et de l’anglais.
Offre :
  • Une fonction diversifiée incluant des responsabilités et des projets intéressants.
  • Des défis professionnels, technologiques et humains enrichissants.
  • Intégrer une structure industrielle renommée et innovante en pleine croissance.
  • Un salaire attractif reprenant des avantages extra-légaux, en ligne avec votre expérience.

Maintenance & Manufacturing Technician - Medical Device - Awans (Liège)

Miracor Medical, a medical device company located in Awans, Belgium, provides innovative solutions for the treatment of severe cardiac diseases, aiming to improve short and long-term clinical outcomes and reduce associated cost.

The company has developed the PiCSO Impulse System, the first and only coronary sinus intervention designed to reduce infarct size, improve cardiac function by clearing microcirculation and potentially reduce the onset of heart failure following acute myocardial infarction.

The technology has received ‘Breakthrough Designation’ from the FDA in 2019 and the CE-Mark in June 2020. Miracor is currently recruiting patients in a landmark European randomized controlled trial, while preparing for a US investigational device exemption study (IDE) and building up team for the upcoming commercialization.

Miracor Medical is now looking for talented and enthusiastic talents to expand its international team. For additional information about the company and its technology, please visit www.miracormedical.com.

Miracor Medical offers a culturally diverse, English speaking working environment in the heart of Europe, Belgium, a few hours away from Europe’s capital cities.

To support the development of the company, we are looking for a (m/f):

Maintenance & Manufacturing Technician

The key objectives of the Maintenance & Manufacturing Engineer are to ensure that the System installation, service and repair activities are planned and carried out on time and that the production of Components is executed as planned. The position is office based in Awans (Liège). Travel to hospitals and other partnering companies in Europe is possible.

Responsibilities:
  • Contribute to the Company Quality Objectives
  • System installation, service and repair management and execution
  • Responsible for the manufacturing (packaging and labelling) of system components.
  • Test equipment management (e.g. monitor calibration needs).
  • Spare parts management (e.g. create technical specifications, perform purchasing and inspection tasks).
  • Assist in verification and validation activities.
  • Other duties as assigned by direct Supervisor

 

Profile:
  • Bachelor’s or master’s degree in Biomedical Sciences, or equivalent through experience.
  • Any experience as a technician or engineer in the Medical Device industry is an asset
  • You are autonomous and have a hands-on and pragmatic mind-set.
  • You are able to work and collaborate effectively with internal and external stakeholders to achieve company objectives.
  • You are able to understand and interpret medical device regulations and Quality Management Systems.
  • You possess excellent communication skills.
  • You would like to work in a dynamic and social environment.
  • You are fluent in English. A good command of French and/or any other language is an asset.
  • Proficiency with common business software, such as MS Office applications.

 

Offer:
  • A challenging and diversified position within a high-potential innovative medical device company.
  • To work in a human size, dynamic, respectful and professional environment.
  • International exposure, with learning and development opportunities.
  • An attractive compensation package in line with the position responsibilities and your experience.

Finance Manager Belgium & Group Internal Controller - Bio-Pharma/Biotech, Biotechnology - Gosselies

iTeos Therapeutics is a privately-held, clinical-stage biopharmaceutical company dedicated to extending and improving the lives of cancer patients by designing and developing next generation immunotherapies. iTeos Therapeutics is advancing its two main programs into a phase I/II clinical stage. The first program is an insurmountable and non-brain penetrant adenosine A2A receptor antagonist. The second program is a human ADCC-enabling anti-TIGIT antibody.

Based in Gosselies, Belgium and Cambridge, MA, iTeos Therapeutics was founded out of the Ludwig Institute for Cancer Research (LICR) and the de Duve Institute (UCLouvain) in 2011. In March 2020, the Company completed a $125 million Series B2 financing led by 6 main US Venture Capitalists. All previous investors including Fund +, VIVES II and SRIW, as well as SFPI, also participated in this funding round. For more information, please visit www.iteostherapeutics.com.

iTeos Therapeutics is now a world-class actor in the sector. To carry on its growth and reinforce its team, iTeos Therapeutics is looking for a (m/f) :

Finance Manager Belgium & Group Internal Controller

Reporting to the US based Finance Director, you are responsible for the overall supervision of all Belgian day-to-day financial activities (including external consultants) and in charge, with the support of external consultants, of the group internal controls.

Main responsibilities:

External reporting

  • Preparation of quarterly and annual US GAAP consolidated accounts (with external consultants)
  • Management of the relationship with external auditors and financial consultants
  • Preparation of the Audit Committee

Budgeting, financial reporting and controlling

  • Supervision of financial book-keeping and external accountants
  • In charge of cost/management accounting
  • Preparation of budgets & plans and monthly, quarterly & annual reporting.
  • Follow-up of expenses and in particular projects or activities related costs, in coordination with the scientific and clinical teams.
  • Identification and analysis of significant gaps between budget and actuals.
  • Forecasts and specific financial analysis requested by top management
  • Presentation to and review of financial position with top management

Tools, systems and procedures

  • Define, implement and maintain adequate internal controls (Sox compliance is foreseen in the future)
  • Selection, implementation & maintenance of accounting and ERP systems
  • Review, development, optimization and implementation of accounting procedures

Taxes

  • Follow up of transfer pricing policy and associated documentation (with external advisors)
  • Follow up of Belgian tax position (with external advisors)

Treasury

  • Treasury forecast, FX risk management
  • payments management.

Support to specific projects such as IPO preparation, Sox implementation and follow-up, etc.

Profile:
  • You hold a University Degree (Master degree in economics, finance or related).
  • You have at least 5 years’ experience in controlling and reporting activities (in the Life sciences sector is a plus). Your latest experience involves internal controls in, ideally, a Sox environment.
  • Demonstrated accomplishments in areas of financial analysis/reporting, budgeting, internal controls, auditing, working capital and cash flow management, forecasting & consolidated reporting, risk assessment and continuous improvement.
  • You have good knowledge of IFRS and/or US GAAP standards.
  • You master Standard Office tools and BOB (or other accounting software) and you are familiar with ERP.
  • You are perfectly fluent in French and English (oral and written).
  • You are willing to travel to the U.S. (possible travels to Boston).
  • Organized and rigorous, you have a good ability to adapt to changes in priorities.
  • Although autonomous, you have a high ability to collaborate with multidisciplinary teams.
  • You are very open-minded and have excellent interpersonal and communication skills.

LEADERSHIP CHARACTERISTICS:

  • Entrepreneurial, resourceful, energetic, self-starter
  • Approaches challenges with creativity and pragmatism
  • Ability to engage team to achieve goals without direct authority
Offer:
  • A stimulating scientific position within a high-potential innovative biotech company.
  • The opportunity to work in a science-driven, dynamic, human‐sized, respectful and professional environment.
  • A challenging scientific and business growth in which you get to bring your knowledge and skills.
  • Varied contacts inside the company, the biotech/pharma sector and the scientific world.
  • A long-term contract and an attractive salary package in line with the position responsibilities and your experience.