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Kwaliteit, Veiligheid en Milieu

7 resultaten

Computerized Systems Validation Specialist - Radio–Pharma - Fleurus

Situées à Fleurus (Belgique), l’Institut National des Radioéléments (IRE) et sa filiale IRE ELiT sont des entreprises industrielles renommées et innovantes.

Avec près de 225 collaborateurs, l’IRE est 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 protection de l’environnement et 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) :

Computerized Systems Validation Specialist

Responsabilités :

Au sein du service Qualification et Validation du département d’Assurance Qualité, vous êtes en charge de la validation des systèmes informatisés du groupe IRE et IRE ELiT et au maintien de ces systèmes en état validé. Vous participerez activement à la mise en place d’une politique de l’Intégrité des Données.

Les responsabilités suivantes vous sont confiées :

  • Concevoir et rédiger/revoir les documents liés aux activités de validation :
    • les exigences utilisateurs (URS) pour l’intégration des requis en VSI : gestion des accès, intégrité des données, sauvegarde et archivage… ;
    • les revues des exigences règlementaires des systèmes informatisés : GMP Eudralex, 21 CFR Part 211, 21 CFR part 11 et EU GMP Annexe 11… ;
    • les évaluations d’impact et classification des logiciels ;
    • les analyses de risques et les matrices de traçabilité ;
    • les plans de validation et les protocoles IQ-OQ-PQ et fiches de tests associées.
  • Coordonner les activités de validation avec les fournisseurs et les départements utilisateurs.
  • Exécuter et/ou vérifier l’exécution des tests de validation réalisée par les utilisateurs, le service informatique et/ou les fournisseurs.
  • Gérer des anomalies et des déviations des tests d’IQ, OQ et PQ.
  • Rédiger des rapports de qualification et des revues périodiques des systèmes informatisés.
  • Donner des formations en validation de systèmes informatisés.
  • Assurer que les systèmes informatisés sont auditables et participer aux audits externes (clients et Autorités de la Santé).
  • Assurer le suivi des indicateurs VSI.
Profil :
  • Vous êtes Informaticien, Ingénieur ou Master, ou équivalent par expérience.
  • Vous disposez de minimum 5 années d’expérience dans la validation des systèmes informatisés dans un environnement GxP.
  • Vous maîtrisez la conduite de projets en laboratoire pharmaceutique dans le respect des exigences réglementaires : GMP et autres normes FDA.
  • Vous possédez une connaissance approfondie en GAMP 5, en FDA 21 CFR part 11 et EU GMP Annexe 11.
  • Vous appréciez les milieux industriels sous contraintes de qualité et de productivité.
  • Vous jouissez d’une très bonne connaissance du français. Une connaissance suffisante de l’anglais est attendue (à l’écrit, au minimum – possibilité de formation si nécessaire).
  • Vous êtes orienté(e) résultats, rigoureux/se, pragmatique, autonome, doté(e) d’une forte capacité organisationnelle et relationnelle.
Offre :
  • Une fonction diversifiée incluant des responsabilités et des projets intéressants.
  • Des défis professionnels et humains enrichissants.
  • L’opportunité d’intégrer une structure industrielle renommée et innovante.
  • Un salaire attractif reprenant des avantages extra-légaux, en ligne avec votre expérience.

Qualification and Validation Project Leader - Radio–Pharma - Fleurus

Situées à Fleurus (Belgique), l’Institut National des Radioéléments (IRE) et sa filiale IRE ELiT sont des entreprises industrielles renommées et innovantes. 

Avec près de 225 collaborateurs, l’IRE est 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 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) :

Qualification and Validation Project Leader

Responsabilités :

Au sein du service Qualification et Validation du département d’Assurance Qualité, vous intervenez dans la définition du projet jusqu’aux étapes de commissioning et de qualification/validation, tant sur les modifications d’installations existantes, que sur la construction de nouvelles installations/unités/nouveaux bâtiments.

Les responsabilités suivantes vous sont confiées :

  • Participer à la définition des projets en intégrant les exigences règlementaires (GMP Eudralex, 21 CFR Part 211, … ).
  • Concevoir et rédiger/revoir les documents liés aux activités de validation :
    • les exigences utilisateurs (URS) ;
    • les évaluations d’impact ;
    • les analyses de risques ;
    • les plans de validation et les protocoles IQ-OQ-PQ et fiches de tests associées.
  • Revoir/ approuver la documentation des fournisseurs.
  • Coordonner les projets sur les activités de validation avec les fournisseurs et les départements utilisateurs.
  • Exécuter et/ou vérifier l’exécution des tests de validation réalisée par les fournisseurs et/ou les utilisateurs.
  • Gérer des anomalies et des déviations des tests de validation/qualification.
  • Rédiger et/ou vérifier les rapports de validation/qualification.
  • Assurer la passation des systèmes de l’équipe projet au détenteur du système.
  • Assurer que les nouvelles installations sont auditables et participer aux audits externes (clients et Autorités de la Santé).
  • Réaliser le suivi et le reporting des indicateurs des projets Q/V.
Profil :
  • Vous êtes Ingénieur ou Master, ou équivalent par expérience.
  • Vous disposez d’environ 10 années d’expérience dans la qualification d’installations et de bâtiments pharmaceutiques.
  • Vous maîtrisez la conduite de projets en laboratoire pharmaceutique dans le respect des exigences réglementaires : GMP et autres normes FDA.
  • Vous appréciez les milieux industriels sous contraintes de qualité et de productivité.
  • Vous jouissez d’une très bonne connaissance du français. Une bonne connaissance de l’anglais est attendue.
  • Vous êtes orienté(e) résultats, rigoureux/se, pragmatique, autonome, doté(e) d’une forte capacité organisationnelle et relationnelle.
  • Vous êtes disposé(e) à vous déplacer ponctuellement.
Offre :
  • Une fonction diversifiée incluant des responsabilités et des projets intéressants.
  • Des défis professionnels et humains enrichissants.
  • L’opportunité d’intégrer une structure industrielle renommée et innovante en pleine croissance.
  • Un salaire attractif reprenant des avantages extra-légaux, en ligne avec votre expérience.

Compliance Specialist - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences, a contract research organisation with facilities in Montreal (Canada), Gosselies (Belgium) and Freemont (USA), 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.

In the context of its growing immune monitoring service offering, Caprion is looking to hire a Compliance Specialist, for its site in Gosselies, Belgium.

Compliance Specialist

Function :

Reporting to the Director of Scientific Operations, the Compliance Specialist (a) monitors and regularly verifies study data to ensure compliance to Caprion SOPs, (b) implements, manages, and maintains procedures for the verification of study data and reports, (c) works closely with Operations and QA to ensure scientific team members and analysts are aware of, and adhere to process updates, (d) provides compliance expertise and guidance to analysts and study directors to ensure the Global Compliance organizational processes are fully optimized.

Tasks include :

  • Work independently to monitor and regularly verify study data to ensure compliance to Quality requirements, and ensure corrections are made appropriately according to Caprion SOPs through data review and in-life audits.
  • Liaise with Operations and QA to identify root cause and resolve anomalies, using existing solutions or creating new ones.
  • Implement, manage and maintain procedures for the verification of study data and reports, including periodic data verifications and review to ensure report accuracy.
  • Train staff on procedures and processes to ensure compliance.
  • Implement procedures in partnership with Operations and QA to streamline and improve documentation/QC process.
  • Use best practices and knowledge to identify opportunities to improve business processes and performance, and advise Operations possible technical solutions.
  • Act as a resource and trainer.
Profile of the applicant :

The applicant must hold a bachelor or master degree (or the equivalent) in a life science discipline such as biology, medical biology or biochemistry/biotechnology.  The applicant must have a minimum of 5 years working in a GLP environment or in an equivalent Quality System.  Auditing experience is an asset.

The applicant must :

  • Have a thorough knowledge of GLP-GDP regulations;
  • Demonstrate excellent oral and written communication skills;
  • Demonstrate excellent organization skills and ability to multi-task to meet deadlines in a fast-paced, changing environment;
  • Be able to work independently, autonomously and as part of a team;
  • Be detailed and process-oriented, meticulous and show commitment to achieve good quality work.
  • Be functional in French and English (spoken and written).
Offer :
  • Full time permanent contract, with possibility of rapid start.
  • A professional, dynamic and stimulating work environment.
  • A competitive salary package including benefits, adapted to your experience and the context.

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.

Expert Qualité Produit - Aéronautique - Sars-et-Rosières

Née d’un projet industriel commun de deux leaders mondiaux de l’industrie aéronautique, Air France Industries KLM E&M et Safran Aircraft Engines, Airfoils Advanced Solutions est une usine 4.0 mettant en œuvre des hautes technologies dans ses procédés industriels et dans ses systèmes d’information. Ce site unique en Europe est dédié à la réparation d’aubes de compresseurs haute-pression de moteurs d’avions de ligne (GE90, CFM56, GP7200).

Implantée sur le Parc d’Activités de Sars-et-Rosières, à 25 min de Lille, Airfoils Advanced Solutions emploie actuellement 50 personnes, avec l’objecitf d’atteindre le cap des 200 employés à l’horizon 2022.

Afin de renforcer son équipe, nous sommes activement à la recherche d’un (h/f) :

Expert Qualité Produit

Responsabilités :

En tant qu’Expert Qualité Produit, vous assurez aux clients de l’entreprise des produits et services de classe mondiale en termes de sécurité, de qualité, de fiabilité et de performance. Rapportant au Responsable Qualité & Sécurité, vous contribuez au développement de la culture qualité et sécurité de l’entreprise.

Vos principales responsabilités sont :

  • Mettre en place les indicateurs, les outils qualité et les procédures de contrôle appropriées.
  • Coordonner les moyens de suivi de la qualité des produits livrés aux clients et de leur conformité pendant les phases d’industrialisation et de production.
  • Assurer l’amélioration continue de la qualité du produit, collecter les problématiques produit/process rencontrées et suggérer des recommandations pour améliorer les instructions et la qualité du produit.
  • Organiser un programme de surveillance (Sondages, Self audits) en vue de vérifier la conformité des produits aux procédures en vigueurs.
  • Être le garant du respect des exigences réglementaires internes/externes et des spécifications normatives applicables.
  • Animer, promouvoir et garantir le respect de la politique Qualité et Sécurité de l’entreprise pour assurer la confiance des clients.
  • Organiser des actions de sensibilisation et de formation du personnel aux problèmes de la qualité.
Profil :
  • Vous possédez 10 ans d’expérience dans les technologies industrielles, telles que la fabrication et/ou la réparation de pièces de moteurs d’avion. A ce titre, vous avez acquis de solides compétences techniques liées aux activités de la maintenance moteurs d’avions.
  • Vous démontrez de bonnes connaissances des activités relatives à la qualité produit/process ainsi qu’une maitrise des outils de qualité (8D ; AMDEC, PDCA, audit,…).
  • Vous disposez d’une réelle aisance relationnelle.
  • Vous appréciez le travail en équipe et êtes capable de mobiliser et fédérer.
  • Vous êtes organisé(e), analytique et faites preuves de bonnes capacités de synthèse et rédactionnelles.
  • Vous êtes disposé(e) à vous déplacer en France.
  • Vous communiquez aisément en français et en anglais.
Offre :
  • Une fonction diversifiée incluant des projets intéressants.
  • Intégrer un site unique en Europe à la pointe du développement.
  • Un salaire attractif assorti d’avantages extra-légaux, en phase avec votre expérience.
  • Un contrat à durée indéterminée à temps plein.

Industrial Pharmacist - Services - Tournai

Our client is a company from Tournai’s area offering a range of laboratory and consultancy services to its clients from pharma, biotech, medtech and hospital areas. Even if mainly active in Wallonia, their expertise and professionalism is already internationally recognized.

To support the company growth, we’re actively looking for an (m/f) :

Industrial Pharmacist

Responsibilities:

Reporting to the Laboratory Manager, you take part to all tasks in relation with the group activities quality assurance.

Your main responsibilities are :

  • Define all flows : products, material, edibles, consumables, wastes.
  • Conduct risk analysis relating to the whole laboratory process.
  • Adapt and complete the documentary system to EU GMP / BPF requirements.
  • Conduct the PVD (rooms and equipments qualification), with the group’s quality service.
  • Implement the verification and validation process of assay reports in accordance with regulatory requirements.
  • Integrate the processes, product quality and staff security in facilities and equipment conception.
  • Audit the system being set up to assess its efficiency on regular basis.
  • Keep informed about new regulations.
  • Inform the laboratory team about new regulations
  • Keep the documentary system, the processes and the operating modes up to date.
  • Ensure quality about processes realization.
Profile :
  • You are an Industrial Pharmacist.
  • You have potentially a first experience in industry.
  • You are passionate about quality assurance and GMP environments.
  • You are rigorous, autonomous, analytic, proactive and organized.
  • You are results, solutions and customer oriented, and like team work.
  • You have a good knowledge of informatic tools.
  • Fluent in English and Dutch. Good knowledge of French is an asset.
Offer :
  • A diversified position with many responsibilities.
  • The opportunity to join a professional and friendly company, and to take part to its strong growth.
  • Significant training, coaching and development opportunities.
  • Full time permanent contract, with a salary package adapted to your profile and experience.

Industrieel Apotheker QP - Bio-Pharma/Biotech - Estaimpuis

HeX Group, opgericht in 2013, is een dienstverlenend bedrijf dat laboratorium- en consultancyoplossingen biedt aan zijn klanten in de farmaceutische, biotechnologische, medtech- en ziekenhuissector. HeX Group is voornamelijk actief in het Waalse Gewest, en zijn expertise en professionaliteit zijn internationaal erkend.

HeX LAB biedt een complete dienstverlening aan met betrekking tot de analyse van microbiologische stalen, of de validatie van materialen, apparatuur en processen voor decontaminatie, desinfectie en sterilisatie. Om meer te weten te komen over de beschikbare expertise, bezoek https://www.hex-group.euof neem contact met ons op via recruitment@pahrtners.be.

Om het Hex LAB-team in Estaimpuis te vervoegen, zijn we op zoek naar een (m/v)

Industrieel Apotheker QP

Verantwoordelijkheden:

Je bent betrokken bij alle taken die verband houden met de kwaliteitswaarborg van de activiteiten van de groep en rapporteert aan de Laboratoriummanager.

Je belangrijkste verantwoordelijkheden zijn:

  • De hele workflow definiëren: producten, personeel, apparatuur, verbruiksgoederen, afval, …
  • Het uitvoeren van risicoanalyses met betrekking tot alle laboratoriumprocessen.
  • Aanpassen en aanvullen van het documentatiesysteem aan de vereisten van de Eu GMP / BPF.
  • De PVD uitvoeren (kwalificatie lokalen en uitrusting), met de kwaliteitsafdeling van de groep.
  • Implementeren van het verificatie- en validatieproces van testrapporten in overeenstemming met de wettelijke vereisten.
  • Processen, productkwaliteit en veiligheid van medewerkers integreren in het ontwerp van gebouwen en apparatuur.
  • Regelmatig het systeem dat wordt ingevoerd controleren om de doeltreffendheid ervan te beoordelen.
  • Op de hoogte blijven van nieuwe regelgeving.
  • Het laboratoriumteam informeren over de nieuwe regelgeving.
  • Het documentatiesysteem, de processen en de werkprocedures up-to-date houden.
  • Instaan voor de kwaliteit bij de uitvoering van processen.
Profiel:
  • Je bent een industrieel apotheker.
  • Je hebt een QP-nummer.
  • Je hebt een passie voor kwaliteitswaarborg en GMP-omgevingen.
  • Je bent nauwkeurig, autonoom, analytisch, proactief en georganiseerd.
  • Je bent resultaatgericht, oplossingsgericht, klant- en teamgericht.
  • Je hebt een goede kennis van informaticatools.
  • Je hebt een zeer goede kennis van het Nederlands, het Frans en het Engels.
Wat wij bieden:
  • Een gediversifieerde functie met veel verantwoordelijkheden.
  • De mogelijkheid om te werken voor een professioneel en aangenaam bedrijf en bij te dragen aan een sterke groei.
  • Opleidings-, ontwikkelings- en coachingmogelijkheden.
  • Een voltijds contract van onbepaalde duur met een salarispakket dat is aangepast aan uw profiel en ervaringsniveau.

Andere loopbaanmogelijkheden

45 resultaten

Senior R&D Project Leader - 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):

Senior R&D Project Leader

Responsibilities:

As a Senior R&D Project Leader, the candidate will lead strategic R&D projects, including software and hardware components and equipment. Reporting to the CTO, the candidate will lead innovation throughout the company.

The positions’s main responsibilities are:

  • Lead strategic R&D projects from concept to commercialization including specifications, design, prototype, industrialisation, manufacturing, and commercial release of software driven electromechanical systems.
  • Ensure resources, processes, procedures and controls are adapted to the projects needs.
  • Lead internal and external project teams with respect to timelines, budgets, quality, safety and business requirements.
  • Analyse the market, select, lead and manage supppliers, vendors, contractors and external partners in order to meet the innovation goals.
  • Understand medical safety requirements, FMEA and risk analysis. Prepare validation plans in line with company documentation, CE and FDA requirements and industry standards.
  • Lead compliance to the Quality Management Systems (ISO 13485 environment).
  • Be a key person of contact for KOL, scientific experts and governmental authorities.
  • Develop appropriate test methods and write protocols and related reports,
  • Report results and work evolution on a regular basis to the top management.
Profile:
  • Engineering Master’s degree in Electronics, electromechanical or related fields.
  • At least 7 years experience in R&D positions within small and large medical devices companies.
  • Expertise in hard- and software technologies and, ideally, also in catheter engineering, including equipment and software validations
  • Excellent project management methodologies and tools.
  • Strong leadership and communication skills together with hands-on and pragmatic mind-set.
  • Proven record of dealing with vendors for electromechanical and software based systems for medical devices,
  • 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.
  • Prone to travel up to 20% of your work time.
  • Despite joining at senior level, be a hands-on person and can lead and manage the team as well as perform some of the work at task.
Offer:
  • A challenging position with a high potential innovative and young medical device company.
  • To work in a human-sized, collaborative and respectful environment
  • Work within a dynamic and experienced team that brings the best out of motivated potentials.
  • An attractive compensation package in line with the position’s responsibilities and your experience.

Inside Sales Engineer - Vente - Ghlin

Detandt-Simon is een familiebedrijf dat actief is in de distributie en installatie van HVAC-apparatuur voor professionals (B2B). Het bedrijf is gevestigd in Ghlin en kent een sterke groei. Detandt-Simon heeft meer dan 40 mensen in dienst, genereert een jaaromzet van meer dan 17 miljoen euro en beschikt ongeveer 25 000 referenties.

Detandt-Simon heeft een uitstekende reputatie op de markt, wordt erkend voor de kwaliteit van zijn diensten en zijn kwalitatieve klantenservice. Voor meer informatie over het bedrijf kunt u terecht op www.detandt.com.

Om zijn Studiebureau te versterken, zijn we actief op zoek naar een (v/m):

Inside Sales Engineer

In samenwerking met de verkopers die actief zijn in het Vlaamse Gewest, speelt je een centrale rol in het Studiebureau en bij Nederlandstalige klanten. Je identificeert technische oplossingen en maakt offertes op basis van de behoeften van de klanten. Je beheert verschillende projecten op basis van jouw vaardigheden.

Verantwoordelijkheden:
  • De bestekken analyseren en passende technische oplossingen voorstellen
  • Specifieke ramingen uitwerken op basis van de verwachtingen en behoeften van de klant.
  • Technisch advies geven aan zowel klanten als interne teams.
  • Deelnemen aan de indienstelling van bepaalde producten, klantentraining en after-sales service.
  • Zorgen voor een adequate follow-up van de ramingen die naar de klanten worden gestuurd.
  • Nauw samenwerken met verkopers die actief zijn in Vlaanderen.
  • Gestructureerd verslag uitbrengen over de voortgang van de projecten en de gevolgde aanpak.

Afhankelijk van jouw affiniteit en vaardigheden kan je meer verantwoordelijkheden krijgen.

Profiel:
  • Je hebt een technisch diploma of gelijkwaardig door ervaring.
  • Je hebt een eerste ervaring in de bouwsector, bij voorkeur in een vergelijkbare functie.
  • Je spreekt vloeiend Nederlands en hebt een goede kennis van het Frans.
  • Je hebt een affiniteit met het schrijven van technische specificaties en met klantenservice.
  • Ervaring in het schrijven van specificaties is een echte troef.
  • Je gebruikt Microsoft Excel en bent in staat om te werken aan een ERP.
  • Je bent nauwgezet, klantgericht en een goede teamspeler.
Aanbod:
  • Een interessante en gediversifieerde functie binnen een erkend bedrijf.
  • De mogelijkheid om deel uit te maken van een dynamisch, aangenaam en professioneel team
  • De mogelijkheid om te werken aan het stimuleren van HVAC-projecten.
  • Een aantrekkelijk salarispakket in lijn met uw ervaring en extralegale voordelen.
  • De mogelijkheid om in Ghlin te werken, of tot 80% van uw tijd thuis te werken.
  • Een voltijds contract van onbepaalde duur.

Field Service Engineer - Medical Device - Belgium

Founded in 1997, Ashby Gorman Baker (AGB) is an independent service organisation that specialised in the maintenance and servicing of Radiology equipment within hospital environment throughout the UK and Belgium and in some other countries around the World. The majority of the business is within Nuclear Medicine, ie the support of gamma cameras and associated workstations.

Ashby Gorman Baker has facilities in the UK and in Belgium (Lokeren). It is one of the largest independent medical imaging support Companies in Europe.

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

Field Service Engineer

Responsibilities:

After an extensive in-house training within AGB’s UK training center, Belgium workshop and by shadowing engineers during their on-site interventions, you provide an excellent customer-oriented service. Reporting to the Belgium Engineering Supervisor, you are home-based and you perform on-site interventions for AGB’s customers based in Belgium.

Your main responsibilities are:

  • Providing service and support for medical imaging equipment. Ensuring that the hospitals have operating medical equipment to treat patients.
  • Performing the routine preventative maintenance on customer’s systems.
  • Attending and rectifying any breakdown as and when they occur and carrying out the appropriate corrective action to provide an optimal service for hospitals’ patients.
  • Performing maintenance operations by repairing system components and fully test them within AGB’s workshop in Lokeren.
  • Conveying and demonstrating the company’s views and philosophy to the customer at all times.
Profile:
  • You hold a Bachelor or Engineer Degree in electronical/electro-mechanical fields.
  • You have excellent practical electronic skills with regard to understanding/reading complex circuit diagrams, soldering skills, use of electronic equipment.
  • You have a good computing and networking knowledge, as well as mechanical engineering.
  • You are fluent in French and English. A good knowledge of Dutch is an asset.
  • You are ready to travel around Belgium.
  • You are flexible concerning working hours, in order to get the job done.
  • You are able to work as part of a team as well as independently.
  • You are curious and eager to learn new engineering skills.
Offer:
  • A challenging and rewarding position within a prestigious branch of engineering.
  • The opportunity to join a company that help improve patients’ life quality in hospitals
  • Strong in-house training, both formal and practical.
  • To work in a young and dynamic company, with good opportunities for career development.
  • An attractive salary package in line with your experience.

Industrial Project Engineer / Project Manager - Technology - Wallonie

Based not far from the Brabant Walloon area, our client is a high-potential technology start-up with a worldwide ambition.

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

Industrial Project Engineer / Project Manager

Responsibilities:

As an Industrial Project Manager, you are responsible for the planning, procurement and execution of the company’s projects. You manage projects related to the core electromechanical business of the company, including new product, manufacturing, quality, and supply chain projects.

Your main responsibilities are:

  • Maintain an overview of the Projects portfolio – from queued to approved projects, budgets, risks, progress and delivery timelines.
  • Ensure project delivery by carefully (retro-)planning tasks, understanding obstacles and risks, and motivating people without direct supervision authority.
  • Perform engineering duties for various technological Design/Development/Field Applications assignments.
  • Lead the weekly sprint review meetings and prepare the project teams to present to the Executive team.
Profile:
  • Degree in Mechanical or Electronics Engineering, Science, or equivalent work experience.
  • At least 6 years of experience, ideally across multiple departments of industrial/technology companies.
  • Successful experience in project execution with demonstrable evidence of managing and successfully delivering technical project portfolios.
  • Affinity with B2B and mechanical engineering technology and components.
  • A project Management certification and/or previous experience with an ERP or CAD system are strong asset.
  • Excellent organisation and good analytical problem-solving skills.
  • Good entrepreneurial, adaptability, and achievement driven skills.
  • Fluency in English.
  • Willing to travel internationally (max 15-20% of the time), mainly in Europe and the USA.
Offer:
  • To join a most-promising Walloon scale-up company with attractive growth possibilities.
  • Opportunity to grow to Project Leader within an electro-mechanical SMB.
  • The opportunity to work in a human-sized, dynamic, respectful and professional environment.
  • An attractive package in line with the position responsibilities and the context.

Technical Advisor - Automotive - Brussels

Based in Brussels (Belgium), FIGIEFA is the European federation and political representative of the independent wholesalers and retailers of automotive replacement parts. Together with its 19 national European Member State members, it represents the interests of more than 30.000 companies trading with vehicle parts, components and accessories throughout Europe.

The aim of FIGIEFA is to safeguard a legislative environment in the EU that provides access to technical information, to the ‘connected vehicle’ and its in-vehicle data as well as to replacement parts/equipment as the basis for free and fair competition in the automotive aftermarket in a rapidly changing automotive technology environment.

In order to support the activities of its office in Brussels, we are currently looking for a (m/f):

Technical Advisor

Responsibilities:

As a Technical Advisor, you manage all technical and ‘connected vehicle’ IT-related dossiers and processes in connection with FIGIEFA’s activities in the area of the automotive aftermarket.

Your main responsibilities are:

  • Advise FIGIEFA in all technical and ‘connected vehicle’ IT-related matters.
  • Participate in meetings (in Brussels or EU) and take responsibility for the management of technical subjects and dossiers (e.g. telematics, EC type-approval legislation).
  • Support the FIGIEFA Secretariat in its information activities and meetings.
  • Advise and prepare answers on upcoming questions from the EU institutions and help in the preparation of position papers.
  • Liaise with FIGIEFA’s partner alliance AFCAR (Alliance for the Freedom of Car Repair in the EU).
  • Communicate with FIGIEFA legal/political experts and work out common strategies, statements, papers and positions.
  • Report results and work evolution on a regular basis.
Profile:
  • You are an experienced automotive technical expert or are experienced in vehicle-related IT technologies around the ‘connected vehicle’ (e.g. telematics and cybersecurity).
  • You are, preferably, specialised in vehicle communication, vehicle design/functionality, diagnostics or contemporary and developing vehicle technologies.
  • You have excellent oral and written communication skills in English and strong interpersonal skills.
  • You are flexible, proactive, and able to work on your own as well as in close cooperation with the FIGIEFA Secretariat.
  • You are able to assess the business consequences of new legislation, automotive technologies and vehicle related services.
  • You are ready to travel frequently to other European countries.
Offer:
  • A challenging position within a multi-national and political environment that tackles a wide range of technical issues.
  • The opportunity to support and promote free and fair competition in the automotive aftermarket and to safeguard a legislative environment at EU level.
  • Various contacts with European and international institutions while representing the interests of FIGIEFA members.
  • An attractive salary package in line with the position responsibilities and your experience.

Responsable d’Equipe - Industry - Mons

Fondée en 2009, JDC Airports est une société spécialisée dans l’intégration de systèmes « Aeronautical Ground Lights ». Leurs sièges opérationnels se trouvent à Harchies (Belgique) et Roissy (France).

Avec près de 70 collaborateurs, JDC Airports est l’un des leaders et un expert dans le balisage aéroportuaire. Leur offre s’étend depuis la conception (bureau d’études) jusqu’à la réalisation et la maintenance des installations.

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

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

Responsable d’Equipe 

Responsabilités :

Rapportant au Responsable Chantiers, vous êtes garant du respect du timing, du bon déroulement et de la qualité des travaux de votre équipe. Vous veillez à ce que tous les ouvriers s’attèlent correctement à leurs tâches au quotidien.

Vos responsabilités principales sont :

  • Préparer, diriger et surveiller le travail des ouvriers.
  • S’assurer de la bonne qualité du travail effectué par l’équipe.
  • Gérer et s’assurer de l’approvisionnement en consommables, machines et outillages.
  • Réaliser le carottage/décaissage, le tirage de câbles et la pose/dépose de feux.
  • Sceller des embases et remplir après rainurage au moyen d’une résine préalablement préparée.
  • Assurer les raccordements électriques et équiper les chambres selon les normes de sécurité.
  • Rapporter de manière hebdomadaire sur l’avancement des travaux.
Profil :
  • Vous êtes titulaire d’un A2 (Électricité, Électromécanique ou Construction) ou équivalent par expérience.
  • Vous possédez minimum 3 ans d’expérience.
  • Vous portez un grand intérêt au domaine de la construction, du balisage aéroportuaire, etc.
  • Vous faites preuve de leadership et êtes doté(e) d’un très bon relationnel.
  • Vous avez de bonnes compétences communicationnelles, tant à l’oral qu’à l’écrit.
  • Vous communiquez aisément en français (tant à l’oral qu’à l’écrit).
  • Vous êtes mobile et prêt(e) à vous déplacer sur les chantiers en Belgique et en France.
Offre :
  • Un challenge varié et socialement épanouissant au sein d’une PME en forte croissance et experte dans son domaine.
  • Opportunité d’intégrer une équipe valorisant votre esprit d’entreprendre.
  • Un contrat à durée indéterminée assorti d’une rémunération attractive ainsi que des avantages liés à votre fonction.

Senior/Principal Scientist - Biotech - Grenoble

Founded in 2014, PDC * line Pharma is a Belgian-French biotech company that is developing a novel class of off-the-shelf cancer immunotherapies. The technology developed by this spin-off of the French Blood Bank (Etablissement Français du Sang, EFS) can be applied to any type of cancer.

After a first-in-human feasibility clinical study in melanoma, PDC*line Pharma is focusing on new candidates to fight other cancers, including lung cancer, with a new clinical trial underway. The company currently employs about 20 people and has an experienced management team. To date, the company has raised more than €17 million in capital and subsidies  and repayable advances.

In order to strengthen the team in Grenoble, we are actively looking for a:

Senior/Principal Scientist

Responsibilities:

Under the responsibility of the CSO, you are responsible for the activities of the PDC*line Pharma R&D laboratory in Grenoble, at both the organisational and scientific level.

Your main tasks are:

  • To continue the study of the mechanism of action of the PDC cell line (PDC*vac) and develop new generations of products
  • Define and validate the conditions of use of products from the PDC*vac in combination with other therapies, preferably immunotherapies
  • Ensure the drafting and validation of study plans, compliance with scheduled experiments, the collection and analysis of results and the drafting of study reports
  • Organize the management and quality of scientific and technical information
  • Contribute to the creation of regulatory dossiers, biological collections, GMO,…
  • Participate in the evaluation and monitoring of R&D partners and service providers, as well as in the development and monitoring of R&D budgets
  • Manage the other members of the R&D team
  • Ensure the company’s scientific monitoring system and participate in the development of the company’s R&D strategy
 Profile:
  • You have a PhD in Science with a minimum of 5 years of experience.
  • You are specialized in Cellular Immunology.
  • You have a good knowledge of antitumor immune response, dendritic cell physiology and cytotoxic cells.
  • You are familiar with the main technologies in cell biology, biochemistry and molecular biology.
  • You have a good knowledge of animal experimentation.
  • You have a strong experience in project management in an industrial environment.
  • You have a very good command of English (fluent English).
Offer:
  • A diversified and management position within a fast-growing start-up.
  • The opportunity to join a human-sized, dynamic and professional environment.
  • An open-ended contract and an attractive salary package in line with your experience.

Research Assistant – Flow Cytometry and Serology - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences is a contract research organisation with facilities in Montreal (Canada) and Gosselies (Belgium). Caprion Biosciences offers analytical services to biopharmaceutical companies ranging from mass spectrometry-based analytical services to the characterization of the human immune response in clinical samples.

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

In the context of its growing immune monitoring service offering in Gosselies (Belgium), we are looking for a (m/f):

Research Assistant – Flow Cytometry and Serology

Function :

Reporting to the Laboratory Manager and working closely with Principal Scientists, you work within a team focusing on the characterization of the cellular (ELISPOT and various flow cytometry assays such as phenotyping of PBMC, detection of intra-cellular cytokines, etc) and of the humoral (ELISA, Luminex, viral neutralization tests, etc) immune response.

Your tasks include :

  • Perform immunoassays according to current standard operating procedures;
  • Participate to the writing and/or to the review of method SOP and worksheets;
  • Manage reagents inventories and orders;
  • Participate to the technical management of the laboratory;
  • Perform work according to internal quality standards, apply relevant Quality System procedures and participate to the continuous improvement of Quality documents;
  • Attend relevant internal training activities;
  • Depending on the experience level of the candidate, additional tasks may include:
    • Act as a leader in the laboratory for specific studies;
    • Work with the Principal Scientist to prepare experimental plans needed for the conduct of immune monitoring assays;
    • Participate in the development and qualification/validation of complex methods;
    • Participate in experiment planning and problem solving.
Profile:
  • You hold a bachelor degree or a master’s degree (or the equivalent) in a life science discipline such as biology, medical biology or biochemistry/biotechnology
  • You demonstrate a relevant laboratory experience.
  • You have theoretical and practical knowledge of techniques related to cellular and humoral immunology. Experience in cell culture and handling infectious materials in BL2+ environment is an asset.
  • You demonstrate excellent organisational skills.
  • You demonstrate schedule adaptability and flexibility.
  • You are willing to actively participate to the generation, the implementation and the continuous improvement of laboratory processes.
  • You are willing to work in a Quality environment (ISO17025, GCLP, GMP) and apply good documentation procedures (GDP).
  • You are functional in French (spoken and written) and have a functional knowledge of written English. Knowledge spoken English is an asset.
Offer :
  • Diversified tasks and responsibilities and interesting projects.
  • A professional, dynamic and stimulating work environment.
  • Continous training and development opportunities.
  • A competitive salary package including benefits, adapted to your experience and the context.
  • Full time permanent contract, with possibility of rapid start.

Production Manager – Medicinal plants - Agro- & Bio-Innovations - Ath

Founded in 2011, BOTALYS is a start-up company specialized in the horticultural production of highly bioactive and innovative medicinal plants.

BOTALYS has developed a unique cultivation method inspired by vertical farming and hydroponics that allows growing better plants. The company produces the most bioactive form of Red Ginseng available at scale and currently explores the possibilities to expand the technology to other bioactive medicinal plants. BOTALYS’ clients include key players from the nutraceutical, cosmetic, food and pharmaceutical industries.

In order to meet BOTALYS’ future challenges, we are currently looking for a (m/f):

Production Manager – Medicinal plants

Responsibilities:

As a Production Manager, you support the company’s fast expansion and you adapt the production capacities. Reporting directly to the CEO, you lead the company’s production plants. You manage and federate the team and make sure the production objectives are met, with respect to costs, timing, health, safety, environment and quality.

Your main responsibilities include:

  • You develop and implement the company’s production short- and long-term strategy.
  • You lead the production teams and you develop your team members.
  • You plan the production needs and you adapt the production capacities and processes.
  • You define the production budgets with the CFO, and you ensure a rigorous follow-up.
  • You manage the suppliers and subcontractors in order to meet the production’s objectives.
  • You implement a continuous improvement plan within the production.
  • You collaborate with the clients and other departments: R&D, Industrialization, and Quality.
  • You report work evolution and results to the management committee.
Profile:
  • You hold a master’s degree in biotechnology, bioengineering or equivalent via experience.
  • You have 5 to 10 years’ experience in a relevant production management position.
  • You have excellent leadership, communication and organizational skills.
  • You show strong analytical skills, applying them to drive strategies and results.
  • You are ideally proficient in working with ERP software.
  • You are rigorous, flexible, able to work autonomously and to multitask.
  • You are fluent in French and English.
Offer:
  • A key position with a lot of challenges, people management and direct impact on the results.
  • To join and evolve in a high potential start-up company.
  • The opportunity to work for a company with ethical values.
  • A full-time permanent contract, with a competitive salary package.

Senior R&D Project Leader (PK-PD) - Biotech, Biotechnology - Gosselies

Founded in 2018, Apaxen develops a unique and innovative class of anti-inflammatory therapeutics with a primary focus on pulmonary arterial hypertension (PAH).

The company plans to perform the preclinical development of its lead compound for the treatment of PAH through the clinics. Concurrently, Apaxen will design and develop the 2nd and 3rd generation of its lead compound in the field of chronic inflammation, oncology and neurology. Apaxen products has the potential to revolutionize the standard of care of PAH and other diseases related to chronic inflammation.

Apaxen has recently raised 3,3 million € through a Serie A funding process and is located in the Brussels South Charleroi Biopark.

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

Senior R&D Project Leader (PK-PD)

Responsibilities:

As Senior Project Leader in charge of non-clinical activities you identify the relevant studies for Apaxen drug candidates. You work closely with external partners, like CRO, to carry on the non-clinical PK/PD and safety studies on Apaxen drug candidates in the best possible manner l. You report to the CEO.

Your main responsibilities are as follows:

  • You define, plan and monitor all the PK-PD and safety studies necessary for the CTA/IND filing of the lead Apaxen drug candidate.
  • You manage the non-clinical PK-PD-safety studies, mostly performed by CRO, and collaborating research centers. This will include:
    • Proposing the studies, reviewing and challenging the proposed study protocols,
    • Closely monitoring the progresses of the studies,
    • Reviewing and the challenging of the draft study reports.
  • You take part in the writing of regulatory documents and take the lead on the non-clinical part for CTA/IND filing.
  • You maintain close interactions with the team in charge of the CMC part of the project
  • You actively monitor research projects (outsourced) of Apaxen.
Profile:
  • You hold a PhD or PharmD or MD.
  • You have a strong knowledge of drug development, with 5 to 15 years of experience.
  • You have experience in carrying NCE up to CTA/IND filing.
  • You are willing to work within a start-up and dynamic structure, a previous experience in the biotech industry is a plus.
  • You are a team player with strong interpersonal skills.
  • You are result-oriented and focus on your objectives.
  • You are rigorous, independent, pro-active with a problem-solving mindset.
  • You are a team player with a good oral and written communication.
  • You are fluent in French and English.
Offer:
  • A challenging and rewarding position within a Start-up.
  • The opportunity to join a company developing a unique and innovative anti-inflammatory for pulmonary diseases.
  • To work in a human-sized, innovative, collaborative and dynamic company.
  • An attractive salary package in line with your experience.