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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.

Console System Engineer - Medical Device - Awans (Liège)

Founded in 2009, CryoTherapeutics is an early stage European innovative company that is now establishing its operations in Awans (Liège). 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 Liège, we are looking for a (m/f) :

Console System Engineer

Responsibilities:

As a Console System Engineer, the candidate will be involved in planning, specifying, designing, developing and testing future versions of the console which controls the catheter operation and provides the user interface.. Reporting to the Project Manager you play a key role in the R&D/innovation activities.

The position’s main responsibilities are:

  • Collaborate with colleagues and physicians in both pre-clinical and clinical environments to evaluate system performance and identify opportunities to improve the technology and its ease of use.
  • Plan and execute design verification testing for consoles and the full console/catheter system.
  • Design improvement and manufacturing of the current generation console, including design evaluation, specification of design changes, design verification and validation, and design support during manufacturing transfer .
  • Support the design of future generation consoles.
  • 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 ensure adherence to timely execution
Profile:
  • Mechanical, Electronic or Biomedical Engineering Masters degree.
  • 5 years experience in electronic system design, development, testing and industrialization, including at least 2 years experience of medical device development.
  • Relevant technical expertise in multi-disciplinary engineering of electro-mechanical systems with software control.
  • Familiar with medical device regulatory requirements, Quality Management Systems and design control processes
  • Experience of working with and managing component vendors and contract manufacturers..
  • 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 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.

Office Manager - Belgian Brewery - Peruwelz

Située à Péruwelz, la Brasserie Caulier produit fièrement ses propres bières depuis plus de 20 ans. L’entreprise garde son esprit familial, tout en bénéficiant d’une nouvelle dynamique entrepreneuriale forte.

L’équipe actuelle, composée de 24 passionnés, brasse des bières vivantes, de caractère et 100% naturelles, appliquant des méthodes de fabrication artisanale. Depuis quelques années la Brasserie Caulier connait une forte croissance et vient de débuter un large programme d’investissements visant à tripler sa capacité de production.

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

Office Manager

Responsabilités :

Rattaché(e) au CFO, vous apportez votre support aux différents services en termes d’administration et d’organisation, et vous contribuez à l’amélioration de l’environnement de travail et à l’accueil des visiteurs.

En tant qu’Office Manager, vous jouez un rôle central dans le fonctionnement de la brasserie.

Vos responsabilités principales sont :

  • Réaliser diverses tâches :
    • administratives : suivi du respect des procédures, mise en page de documents, suivi des échéanciers administratifs et légaux, etc.
    • liées à la comptabilité : suivi des fournisseurs, encodage, classement, archivage, etc.
    • liées aux ressources humaines : entrées, sorties, prestations, fiches de paie, etc.
  • Assurer le suivi de la boite mail générale et des communications téléphoniques.
  • Accueillir et orienter les visiteurs au sein de la Brasserie.
  • Prendre en charge les demandes liées aux locaux, et réaliser les commandes de matériel et fournitures.
  • Organiser des réunions, team-buildings, évènements et des déplacements/voyages/salons/foires.
Profil :
  • Vous êtes titulaire d’un Bachelier ou d’un Master, ou équivalent par expérience.
  • Vous disposez au moins d’une première expérience dans une fonction comparable.
  • Vous vous épanouissez dans un rôle de support à l’équipe.
  • Vous démontrez une certaine aisance avec les outils informatiques (MS Office, Gmail, etc) et un ERP.
  • Vous maitrisez le français et possédez un très bon niveau en anglais et/ou néerlandais (oral et écrit).
  • Vous gérez adéquatement les priorités et avez le sens de l’organisation.
  • Vous êtes rigoureux(se), flexible et autonome. Vous faites preuve d’initiatives et êtes proactif(ve).
  • Vous disposez d’une excellente communication et faites preuve d’une bonne résistance au stress.
Offre :
  • Une fonction diversifiée au sein d’une PME familiale en forte croissance.
  • L’opportunité de rejoindre un environnement à taille humaine, dynamique et professionnel.
  • L’opportunité d’apporter un support efficace qui sera apprécié par toute l’équipe.
  • Un contrat à durée indéterminée à temps plein, avec possibilité de débuter par un temps partiel.
  • Un package salarial attractif en phase avec votre expérience.

Laboratory Manager - FMCG, Food Services - Spa

Leader du marché dans le Benelux, SPADEL est spécialisé dans la production et la commercialisation d’eaux minérales naturelles, d’eaux de source, d’eaux aromatisées et de limonades. Spadel doit notamment son succès à ses marques Spa et Bru.

En tant qu’entreprise familiale indépendante belge, la société compte plus de 1.300 collaborateurs actifs dans 4 pays (Belgique, France, Royaume-Uni et Bulgarie). Rejoindre Spadel, c’est rejoindre une équipe une équipe dont les valeurs sont Togetherness, Agility, Ownership et Excellence.

Spadel dispose d’un laboratoire de référence dans le domaine de l’eau et des limonades. Ce laboratoire, basé à Spa, est animé par une équipe de huit personnes.

Afin de renforcer la pétillante équipe de Spadel, nous sommes à la recherche d’un (m/f) :

Laboratory Manager

Responsabilités :

En tant que Laboratory Manager, vous dirigez le laboratoire, ses opérations quotidiennes ainsi que son équipe. Vous participez à la définition et la mise en œuvre des méthodes d’analyse utilisées. Vous supervisez une équipe de 6 analystes de laboratoire.

Vos principales responsabilités sont les suivantes :

  • Organiser les activités du laboratoire en s’adaptant aux délais et aux besoins des autres départements.
  • Fournir un support technique aux membres de l’équipe dans les analyses.
  • Interpréter et exploiter des résultats d’analyses et des données statistiques.
  • Définir et adapter des procédures et méthodes d’analyses de contrôle.
  • Veiller à la bonne gestion budgétaire du matériel de laboratoire (remplacement et fonctionnement des équipements).
  • Identifier et diagnostiquer les dysfonctionnements et/ou les anomalies et proposer des solutions pertinentes.
  • Travailler en étroite collaboration avec les membres de tous les laboratoires de Spadel.
Profil :
  • Vous êtes titulaire d’un Master en (micro)-Biologie, Chimie ou Biochimie.
  • Vous possédez une expérience réussie de 5 à 10 ans dans un laboratoire.
  • Vous possédez une excellente maitrise de la norme ISO 17025.
  • Vous êtes familier(ère) aux principes d’analyse (ex : HPLC, ICPNS, microbiologie pathogène, etc.).
  • Vous êtes autonome, rigoureux(se) et organisé(e).
  • Vous êtes habitué(e) à travailler dans un environnement structuré et exigeant.
  • Vous communiquez aisément en français et en anglais (oral et écrit).
  • Vous êtes ouvert(e) à vous déplacer ponctuellement vers les autres laboratoires du Groupe (2 à 3 fois/an).
Offre :
  • Une fonction challengeante au sein d’un laboratoire doté d’un matériel à la pointe de la technologie.
  • Intégrer une entreprise aux fortes valeurs qui priorise le développement durable.
  • Un contrat à durée indéterminée à temps plein.
  • Un salaire attractif assorti d’avantages extra-légaux, en phase avec votre expérience.

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.

Développeur Python – Junior - Electronique automobile, Engineering - Perwez

Créée en 2008, ShifTech Engineering est une entreprise spécialisée dans le domaine de la préparation de moteur sur banc de puissance. Composé d’une équipe de 15 personnes, ShifTech Engineering est actuellement présent en Belgique, en France, au Luxembourg et en Chine, et jouit d’une renommée internationale pour la qualité de ses réalisations et services destinés aux particuliers. Pour plus d’informations sur l’entreprise, veuillez consulter www.shiftech.eu.

Shiftech Engineering souhaite renforcer son équipe, à Perwez, pour consolider son expertise. Dans ce cadre, nous sommes activement à la recherche d’un (m/f) :

Développeur Python – Junior

Responsabilités :

En collaboration avec le motoriste et l’ingénieur en R&D, vous participez aux activités de développement d’outils innovants pour l’entreprise. Vos principales responsabilités sont :

  • Analyser, développer et améliorer les outils informatiques déjà existants permettant la recherche de modèles, séquences et données dans un fichier binaire issu de données d’un calculateur moteur. Cette recherche utilise des outils mathématiques de la librairie Numpy.
  • Etre en charge du développement du logiciel (Python) et de la librairie.
  • Rapporter et présenter de manière structurée, rigoureuse et adaptée les résultats des activités.
Profil :
  • Vous êtes Bachelor ou Master en IT.
  • Vous disposez idéalement de 1 à 3 années d’expérience dans une fonction IT en milieu industriel. Les profils juniors sont également les bienvenus.
  • Vous possédez une bonne maîtrise de Python. Maitriser Javascript, MatLab et Numpy est un atout.
  • Vous faites montre d’un bel intérêt pour l’esprit start-up qui encourage la créativité et l’innovation.
  • Vous aimez les challenges et vous montrez de réelles affinités pour l’automobile.
  • Vous communiquez aisément en français et, idéalement, en anglais aussi.
  • Vous êtes analytique, proactif(ve), autonome, organisé(e) et rigoureux(se).
Offre :
  • Une fonction technique stimulante dans une petite équipe jeune et dynamique.
  • Intégrer une structure en pleine expansion, renommée dans le domaine automobile pour la qualité de ses services.
  • Un cadre de travail agréable et d’accès aisé, et la possibilité de homeworking une à deux fois par semaine.
  • Un contrat à durée indéterminée à temps plein en Belgique (Perwez).
  • Des opportunités de formations et de développement.
  • Une offre salariale attrayante, assortie d’avantages extralégaux compétitifs comprenant entre autres une voiture de société.

Head of Pharma Development - Bio-Pharma/Biotech - Mont-Saint-Guibert

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

Based in Mont-Saint-Guibert (30km from Brussels) and reinforced by its 21 million euros fundraising success, A-Mansia is searching for a dynamic and enthusiastic person to strengthen the team. For more information about the company and the technology, please contact us via recruitment@pahrtners.be.

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

Head of Pharma Development

As a “Head of Pharma”, you lead the company’s therapeutic protein development program(s) from preclinical to clinical stages. Reporting to the CEO, you are responsible for strategic initiatives to bring our very promising investigational product to clinical proof of concept by combining internal and external resources.

Your main responsibilities are as follows:
  • Lead A-Mansia’s pharmaceutical development and manage its drugs development portfolio.
  • Manage regulatory preclinical and early clinical development of company’s lead products.
  • Manage internal scientific team and external collaboration to achieve A-Mansia’s strategic results.
  • Participate in the crafting of business development messages and packaging of the scientific data in view of potential Pharma partnerships.
  • Promote innovation and interact with research teams (internal and external)
  • Be part of the COMEX, which requires offering help and advice on all of the company’s projects and strategic questions, and report to Board of Directors on the strategic development of operations
Profile:
  • You are Ph.D, DVM or MD with at least 10 years of experience in pharma development.
  • You have an experience and expertise in protein development as IMPD.
  • You have already led ‘translational’ development program(s) from preclinical to early clinical stages.
  • You are recognized as a pragmatic and result driven manager and you look for a hands-on position in a cutting-edge scientific field.
  • Knowledge of the microbiota field would be a plus.
  • Rigorous, detail-oriented, autonomous, committed and flexible.
  • Excellent oral and written communication skills in English and French. The command of Dutch is a plus.
  • Strong team spirit and excellent interpersonal skills
Offer:
  • A strategic and leading position with a high potential innovative and young biotech company
  • To work in a human-sized, collaborative and respectful environment
  • To take part in a challenging and cutting-edge development program
  • An attractive compensation package in line with the position’s responsibilities and your experience.

Software Engineer - Green-Tech - Liège

SmartNodes is a Belgian innovative green-tech start-up active in the smart cities’ sustainable development.

Based in Liège, SmartNodes develops smart street lighting solutions based on high-tech controllers to power street lighting only in presence of road users.  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 City networks. Please visit www.smartnodes.be.

SmartNodes’ customers are cities, regions and distribution network companies, worldwide. In order to develop its business, we are actively looking for an (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.
  • 3 to 5 years’ experience in a software engineer position within the industry.
  • Good understanding of Linux environments.
  • 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.
Offer:
  • A diversified and challenging technical position within a dynamic 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.

Production Manager - 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

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.

Research Assistant – ChromaCure - Chemicals, R&D Medical & Science - Gosselies

ChromaCure is a biotech company focusing on oncology drugs development. The mission of ChromaCure is to provide innovative solutions based on small molecules therapeutics.

Based in Gosselies (40km from Brussels) and reinforced by its 17 million euros fundraising success, ChromaCure is searching for a dynamic and enthusiastic person to strengthen the team. For more information about the company and the technology, please contact us via recruitment@pahrtners.be.

ChromaCure offers a French and English-speaking environment, culturally diversified and located in the heart of Europe, in Belgium, within easy reach of several European Capitals.

To strengthen the team in Gosselies, we’re looking for an (m/f):

Research Assistant

As a Research Assistant, you execute cellular and molecular biology in order to contribute to ChromaCure’s drug development program from target validation to development of innovative cancer immunotherapies.

Your main responsibilities are as follows:
  • Maintain, amplify, and transfect mammalian cell lines
  • Develop, validate and run in vitro assays.
  • Run western blots, cell lysis, and immunoprecipitations
  • Perform routine molecular biology (RNA extraction, DNA cloning)
  • Collaborate and contribute to the ongoing activities and with other team members
  • Compile data, analyse, summarise and present experimental results.
  • Report work evolution on a regular basis.
  • Perform bibliographic research.
Profile:
  • You hold a Bachelor’s or Master’s degree in biology and biomedical sciences.
  • You have preferably 3 years of experience in the biotech/pharma industry.
  • You will have an excellent knowledge and hands-on experience with cell culture, molecular biology, and assay development.
  • You are rigorous, detail-oriented, autonomous, committed and flexible.
  • You show good oral and written communication skills in English (and ideally also in French).
  • You have strong team spirit and excellent interpersonal skills.
Offer:
  • A diversified scientific position within a high-potential innovative biotech company.
  • To work in a human-sized, innovative, collaborative and respectful environment.
  • To take part in a challenging and cutting-edge development program.
  • An attractive compensation package in line with the position’s responsibilities and your experience.