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Consultance RH

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Stagiaire en Recrutement - Consultance RH - Mont-Saint-Guibert/ Saint-Georges-sur-Meuse

PaHRtners est une entreprise belge de consultance en Ressources Humaines (RH). Nos bureaux sont situés à Woluwe-Saint-Lambert (Bruxelles), à Gosselies, à Saint-Georges-sur-Meuse (Liège) et à Mont-Saint-Guibert (Wallonie).

Nous sommes notamment spécialisés dans le recrutement et la sélection de scientifiques, d’ingénieurs, d’experts et de top managers. Nous fournissons ces services principalement aux secteurs industriels et de la santé.

Les valeurs-clés sur lesquelles repose notre approche sont l’authenticité, la transparence et le respect. Consultez www.pahrtners.be ou contactez info@pahrtners.be pour plus d’info.

Pour renforcer l’équipe dans notre bureau de Mont-Saint-Guibert ou de Saint-Georges-sur-Meuse, nous recherchons actuellement un(e) :

Stagiaire en Recrutement

– pour 4 à 6 mois –

Tâches :

En tant que stagiaire, vous recevrez tout d’abord une solide formation. Sous la supervision du responsable de stage, vos principales tâches seront les suivantes :

  • Exploiter les outils modernes de recrutements : réseaux sociaux, bases de données, approche directe, cooptation, etc.
  • Rédiger et publier des annonces sur les sites Internet.
  • Participer au sourcing, screening et à la pré-sélection des profils identifiés.
  • Contacter les profils identifiés et assurer un suivi professionnel tout au long de la procédure.
  • Réaliser des prises de références professionnelles.
  • Participer aux entretiens de sélection, et débriefing.
  • Assister aux Assessment/Development Centers et analyser les compétences.
  • Assurer une bonne gestion administrative des dossiers de recrutement.
  • Réaliser des projets visant l’amélioration du service.
Profil :
  • Bachelor ou Master en RH, Psychologie, Business, Sciences ou Ingénieur.
  • Une réelle motivation à découvrir le monde du recrutement et de la chasse de têtes.
  • Un intérêt pour le monde industriel et scientifique.
  • Rigoureux(se), autonome et proactif(ve). Convivialité et curiosité intellectuelle.
  • Bonne communication en Français. L’anglais et le néerlandais sont des atouts.
  • Disposé(e) à vous rendre à Mont-Saint-Guibert (Wallonie) ou à Saint-Georges-sur-Meuse (Liège) par vous-même.
  • Aisance avec l’informatique et le web.
Offre :
  • Un stage de 4 à 6 mois en recrutement au sein d’une structure professionnelle.
  • Une solide formation reconnue dans le monde du recrutement.
  • Une réelle opportunité d’apprentissage et de réalisations concrètes.
  • Une opportunité de travailler sur des recrutements locaux et internationaux.
  • Un accompagnement individualisé et une autonomie grandissante.
  • Des horaires flexibles et modulables, une ambiance de travail ouverte et décontractée.
  • Un démarrage de stage selon vos préférences.

Other career opportunities

44 results

Electric Motor control Engineer - Engineering, Innovation, Transport - Genval

Founded in 2013, E2 Drives is an innovative start-up company active in electric mobility. The company is specialized in mechanics, electronics, electric motor and embedded control software. Recently, E2 Drives has developed a high-end and disruptive new generation of electric bikes. The key differentiator of the bike is its all-in-one drive unit integrating an electric assistance and an automatic gearbox.

E2 Drives’ ambition is to develop and commercialize the best electric bike on the market, in the commuting segment, with premium functions and an affordable price. The team is currently composed by 5 dynamic and entrepreneurial persons but will strongly grow this year.

E2 Drives, future top player of the electric bikes market, is based in Genval (South-East of Brussels).

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

Electric Motor control Engineer

Responsibilities:

Reporting to the CTO, you develop embedded firmware for the motor control PCB. Based on internal objectives, you, on one hand, focus on tasks as improving motor control performance and on the other hand identify and implement more broader algorithm to control the whole drive unit of the electric bikes.

Your main responsibilities are:
  • You will propose and draw up the roadmap and its implementation in C of the electric motor control and more broadly the drive unit control.
  • You improve step response, improving efficiency, lowering ripples, increasing torque per ampere of our current PMSM FOC (also called dq, vector) control.
  • You adapt our control to IPM motor.
  • You lead C firmware developments, maintain, upgrade with regards to quality, robustness (by failure analysis) and timing.
  • You are in charge of your own projects and collaborate within the software development team.
  • You report work evolution on a regular basis.
Profile:
  • Master degree in engineering or equivalent through experience.
  • 3 to 5 years’ experience in a software engineer position within the industry.
  • Experience in time-critical C firmware development, PMSM and IPM control (FOC) and its low level constaints (Timing, Sampling, Filter delays, PWM updates opportunity…). Git or SVN familiar.
  • Analytical, problem solving skills, rigorous, autonomous and results oriented.
  • Familiar with failure analysis and code robustification.
  • Command of bootloader, authentification, and encrypted firmware updates are major assets.
  • Knowledge in STM32 and/or Kinetis families’ peripherals is a plus.
  • Fluent in French or in English.
Offer:
  • A diversified and challenging technical position within a experienced team in a fast growing start-up.
  • The opportunity to enter a sustainable development and green tech company.
  • Varied contacts with professionals on an international scale.
  • Significant learning and evolution opportunities.
  • An attractive salary package coherent with your experience.
  • A full-time permanent contract.

Software Engineer - Green Technologies, Green-Tech - Liège

Based in Liège, SmartNodes is the LACROIX City R&D excellence center for smart street solutions over lighting grids. The measurement of traffic density and user speeds is used for road mobility and safety applications.  By integrating environmental sensors, parking sensors, etc., SmartNodes’ public lighting network is becoming the driving force behind Smart street networks.

SmartNodes is part of LACROIX City, European leader in Smart City technology. As industrial designer of complementary smart street equipment for local authorities and businesses, LACROIX City guides, optimizes and secures the flow of vehicles and people with an end goal: to share streets and roads, taking into account the needs of all their users and operators. Established in France, Spain, Belgium and North America, LACROIX City has now more than 600 employees shared between R&D offices and complementary production sites. Lacroix City customers are cities, regions and distribution network companies, worldwide. Together, they prepare the infrastructure for smart roads and mobility. Please visit https://www.lacroix-city.com

In order to develop its business and reinforce the team in Liège, we are actively looking for a (m/f):

Software Engineer

Responsibilities:

Reporting to the R&D Manager, you are developing backend applications and SmartNodes embedded communication technologies. You maintain close contact with Sales & Marketing in order to identify technical upgrade of current solutions and commercial opportunities.

Your main responsibilities are:

  • You propose, with the support of the R&D Manager, the roadmap of backend and embedded applications.
  • You develop, maintain and upgrade backend and embedded applications and/or you customize existing standard applications to the most suitable solution based on the customers’ specifications and expectations.
  • You participate to demonstrations and software development projects.
  • Your report work evolution on regular basis.
Profile:
  • Master degree in engineering, IT or computer science, or equivalent through experience.
  • Good understanding of Linux environments and embedded C.
  • Solutions, quality, innovation and results oriented, with good communication skills.
  • Self-motivated, team player, hands on, autonomous, rigorous and flexible.
  • Very good command of English.
  • The command of French, Dutch and/or German is a plus.
  • Junior application welcome.
Offer:
  • A diversified and challenging technical position within a dynamic team in a leader company.
  • The opportunity to enter a sustainable development and green tech company.
  • Varied contacts with professionals on an international scale.
  • Significant learning and evolution opportunities.
  • An attractive salary package coherent with your experience.

Dessinateur/Projeteur - Industry - Bernissart (Mons)

Fondée en 2009, JDC Airports est reconnue comme un leader et un expert dans le balisage aéroportuaire.
Les activités de JDC Airports répondent à des enjeux forts d’un aérodrome liés à la sécurité, le trafic aérien et l’empreinte écologique.

La politique de JDC Airports est orientée sur le dynamisme et le service à la clientèle, tant au niveau national qu’international. JDC Airports propose une structure flexible, un personnel expérimenté et certifié. Pour plus d’informations, veuillez consulter www.jdc-airports.com

Avec près de 70 collaborateurs, JDC Airports propose une large gamme de services allant depuis la conception (bureau d’études) jusqu’à la réalisation et la maintenance des installations. Leurs sièges opérationnels se trouvent à Harchies (Belgique) et Roissy (France).

Afin de soutenir la croissance de JDC Airports sur son site à Bernissart (Mons, Belgique), nous sommes à la recherche d’un (h/f) :

Dessinateur/Projeteur

Responsabilités:

En tant que Dessinateur/Projeteur en Electricité, en lien direct avec les Responsables d’Affaires et les Conducteurs de travaux, vous aurez en charge les études techniques. Vous établissez des plans et schémas électriques, des calculs d’éclairement et divers autres projets clients.

Vos principales responsabilités sont :

  • Réaliser des schémas et des plans électriques.
  • Gérer des dossiers d’exécution et des ouvrages exécutés.
  • Réaliser des relevés et métrés pour la réalisation des plans.
  • S’occuper du dimensionnement des réseaux (note de calculs BT).
  • Etablir des calculs d’éclairement (intérieurs et éclairage public).
  • Mener des études techniques des projets d’appel d’offre Balisage lumineux ou Tertiaire.
Profil:
  • Vous possédez un diplôme technique A2/A3 en électromécanique ou électricité.
  • Vous présentez une première expérience réussie dans un poste similaire.
  • Vous êtes autonome, rigoureux/se, organisé(e).
  • Vous êtes doté(e) d’un bon esprit de synthèse et une bonne capacité d’adaptation.
  • Vous maitrisez AutoCAD et les logiciels de bureautique (Word, Excel).
  • La connaissance des logiciels de calculs Caneco et DiaLUX, ainsi qu’une bonne connaissance technique des normes C15-100 et C13-100 est un plus.
Offre:
  • L’opportunité de rejoindre une société dynamique et en pleine croissance.
  • Une fonction technique, proche du terrain.
  • Un contrat à durée indéterminée assorti d’une rémunération attractive ainsi que des avantages liés à votre fonction.

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.