Jobs

PaHRtners est une entreprise belge de consultance en Ressources Humaines (RH). Nos bureaux sont situés à Woluwe-Saint-Lambert (Bruxelles), à Gosselies 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, 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 Woluwe-Saint-Lambert ou à Gosselies 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.

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):

Business developer – Smart-cities

Responsibilities:

Reporting to the Business Development Manager, you expand SmartNodes’ business on an international scale, mainly in Germany and DACH region. In your assigned region, you develop the attractiveness of the brand on the market, and you reach the company’s sales targets.

Your main responsibilities are:

• You analyse the market evolution, and identify business growth opportunities and risks.
• You propose relevant sales actions plans in order to meet the sales objectives.
• You initiate positive relations with prospects, customers and sales channels.
• You lead all the sales process, including response to call for tender and deal closing.
• You build, support and motivate an efficient sales network of local partners.
• You develop adapted local marketing tools and actions.
• You report work evolution on a regular basis.

Profile:

• Master degree in Business, Engineering or equivalent through experience.
• Ideally first level experience in a sales & marketing position with technical products. Junior profiles are also welcome.
• Results and customer oriented, rigorous, autonomous and flexible.
• Willing to deal with public sector oriented sales activities.
• You are ready to travel around 50% of your work time.
• Fluent in English and German. The command of French and any other language is an asset.

Offer:

• A challenging business development position 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 including a stock options plan.

Miracor Medical is a class IIb/III medical device company specialized in improving clinical outcome of patients with impaired cardiac function, active in interventional cardiology. The company has developed a high potential proprietary technology that consists of hardware, software and catheter(s).

The technology is in advanced clinical stages, with various potential therapeutic applications (among others acute infarct and heart failure). More than 190 patients have been treated with the recent version of the technology. The company aims at getting CE Mark and approval from FDA to run a pivotal study in the next 2 years. 

Miracor Medical’s offices are based in Awans, Belgium. The company is now looking for talented and enthusiastic talents to expand its international team. For additional information about the company and its technology, please visit www.miracormedical.com.

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

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

Clinical Application Specialist

Responsibilities:

• You support clinical trial site selection and qualification of investigators.
• You facilitate and support patient recruitment, selection and enrollment.
• Geographic focus: UK and occasionnally other EU countries
• You assist in clinical cases and ensure that physicians and staff are well trained and educated with regards to patient selection, treatment planning, optimum use of system, etc.
• You work closely with the research team to ensure that all protocol required procedures and visits occur according to protocol specified guidelines and timely entry of the data in the electronic database.
• You represent the company in all regulatory and third party audit requests for clinical trial information.
• You deal with product-related site request and solve issues.
• You engage with physicians and clinical staff, build relations and credibility to be a high level spokes partner.
• You create and maintain effective partnerships with KOL.
• You report results and work evolution on a regular basis to your line manager.

Profile:

• Master’s degree in Biomedical Sciences, Bioengineering or any related field.
• 3-5 years minimum in the management of pre- and post-market medical device studies (class III) at country or European level.
• Hands-on experience in clinical support for cardiovascular medical devices, and ability to direct cases in cath lab.
• Experience introducing disruptive technology, which somehow changes the way clinicians operate.
• Experience in directing, training physicians and staff to stand-alone level.
• Flexible, roll-up-sleeves attitude, self-directed and willing to travel frequently.
• Keen interest in scientific and technical issues related to clinical study.
• Ability to work and collaborate effectively with internal and external actors to achieve company objectives.
• Fluency in English, ideally living in the UK.

Offer:

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

NOVADIP-BIOSCIENCES is an innovative biotech company, based in the Walloon Region (Mont-Saint-Guibert), with a strong expertise in the development of novel regenerative medicines. This human-sized structure is a leader in first-in-class treatments for hard and soft tissues.

If you are sharing their vision of developing life-improving and life-saving products and if you are looking for new challenges amongst a dynamic and innovative team, consider collaboration with their fast growing company.

In order to support its exciting development, we are looking for a (m/f):

Senior Process Optimization Engineer

Responsibilities :

As a Senior Process Optimization Engineer, you will be involved from design to validation, in the development of new manufacturing processes adapted to innovative cell therapy products.

Your main responsibilities are:

• Provide leadership to work on development and continuous improvement of the manufacturing process.
• Define industrial requirement for process automation in cGMP environment (technical and functional specifications).
• Consulting engineering and/or equipment suppliers for development of automated close systems in production and quality control of cell-based therapies.
• Set-up of development projects, coordination of external and internal dedicated team (ensure that industrial requirements and biological constraints are well understood), follow-up of projects execution, budget and reporting.
• Contribute in implementation of new technologies and establish process validation plan in accordance with quality requirements and guidelines.
• Set-up comparability studies to increase the operational scale of autologous manufacturing process (scale-out).
• Ensure technology watch of the state-of-the-art technologies in process industrialization and automation of Advanced Cell Therapy Medicinal Products.
• Manage selection of technologies and act as a scientific expert to ensure good decision making within the department.

Profile :

• Engineer or PhD in Biology, Biochemistry, Biomedical Sciences or other related scientific field.
• At least 5 years of relevant experience in the GMP biotech/pharmaceutical industry.
• At least 5 years of relevant experience in process development in the field of cell therapy.
• Strong knowledge of stem cell biology and processes for cell culture.
• Strong knowledge of industrialization strategies and automation solution for cell therapy production.
• Strong knowledge of quality requirements (GMP, clinical trials, comparability studies, process validation, aseptic practices) and working knowledge of requirements for aseptic manufacturing.
• Ability to provide leadership and to manage priorities, follow assignments through to completion and meet deadlines.
• Ability to work in a team and collaboratively in a matrix organization (R&D, QC, QA, RA).
• Flexible for travelling, organized and pro-active.
• Excellent oral and written communication skills in English, and ideally also in French.

Offer:

• A diversified full-time permanent position within a high-potential innovative biotech company.
• To work in a human-sized, dynamic, respectful and professional environment.
• The opportunity to take part in a challenging scientific and business growth.
• An attractive salary package in line with the position responsibilities and your experience.

Headquartered in Liège, Dim3 develops and markets innovative eHealth software and devices in the area of Clinical nutrition to facilitate medical decisions and enhance the life of patients.

Dim3’s technologies bring a great knowledge of healthcare and clinical biometry together with disruptive 3D scanning and software engineering experience. Dim3’s clinical nutrition management tools and connected products integrate automatic medical data collection, interpretation and visualization to give healthcare professionals clear and objective information in real-time.

For more information, please visit: www.dim3.com

In order to support Dim3’s development, we are actively looking for a (m/f):

Product Specialist

Responsibilities:

As a Product Specialist, you guide Dim3’s products to even higher levels. You have a key role in the team. You deal with medical practitioners, customers and partners in order to determine the future direction of Dim3’s applications including specific features, functionality and business models. You deeply understand the pains patients feel and invent ways to translate their needs into smart software.

Reporting to the CTO, you work in close cooperation with customers, the Management Team, Product Development, Clinical Affairs and Sales. Your main responsibilities are:

• You initiate the product roadmap and strategy in line with market needs and business priorities.
• You define the pricing strategy and constantly analyze market trends and competitors’ evolution.
• You support the Sales team in analyzing customers project requirements, in defining adapted technical solutions, and in developing written and oral commercial proposals.
• You define new products specifications or improvements in an efficient way.
• You manage the release process in collaboration with the other departments.
• You develop adapted local marketing tools and actions.
• You report work evolution on a regular basis.

Profile:

• Master’s degree in Business, Engineering or equivalent through experience.
• 5 years of experience in a Product Management position with technical products. Experience in medical software and/or devices is a plus. Experience in nutrition is also an asset.
• Results and customer oriented, rigorous, autonomous and flexible.
• Analytical, organized, team player, open-minded with a start-up mind-set.
• Fluent in French and in English. The command of any other language is an asset.
• Strong oral and written communication.
• Willing to travel for short periods (20% of your time) on a regular basis.

Offer:

• A challenging position with direct impact on patients’ health and quality of life.
• The opportunity to jump into an innovative medical software engineering company, a fast-growing start-up environment where teamwork, results and patient care are very important.
• Varied contacts with professionals on an international scale.
• Significant learning and evolution opportunities.
• An attractive salary package.

Known as one of the 5 « Supermajors », our client is a top player in the global oil and gas industry, as well as a leader in industrial chemistry.

In an increasingly competitive environment due to imports of commodity products, and in order to protect its intellectual property and secure its catalytic developments, our client has decided to develop, produce and sell metallocene catalysts.

In order to ensure the development of our client’s polymer plant located in the south of Brussels, we are actively looking for a (m/f):

Manufacturing and Industrialization Manager

New Generation Catalysts

Responsibilities:

As a Manufacturing and Industrialization Manager of New Generation Catalysts, you coordinate the start-up of the production unit of these catalysts. Reporting to the Executive Committee, you are the technical referent and you supervise the production team.

The following responsibilities are entrusted to you:

• Coordinate and optimize catalyst production in terms of resources, process and results, according to the required specifications.
• Optimize the application of new process and catalytic versions, in close collaboration with the research and the process department.
• Maximize the production unit financial profitability by ensuring cost reduction (debottlenecking, solvent recovery, etc.).
• Implement and ensure compliance with quality (QC/QA) and safety standards.
• Implement a procedure and ensure performance monitoring.
• Collaborate closely with the supply chain.
• Be the technical responsible for the catalysts purchased from tollers.
• Ensure the customer follow-up worldwide in terms of performance.
• Supervise, motivate and develop the production team.

Profile:

• You have a Master’s degree/PhD in Chemistry.
• You have at least 10 years of experience in scale-up and industrial manufacturing of polyolefin catalysts. As such, you have acquired a solid knowledge in polymerization, and ideally in downstream applications.
• You have experience in the management of a catalyst operating team (pilot/industrial unit).
• You are comfortable with project management and you enjoy teamwork.
• You are autonomous, rigorous, with a strong ability in decision-making and leadership.
• You have a very good command of English.
• You are willing to travel occasionally on all continents.
• You are ready to relocate internationally.

Offer :

• A strategic and diversified position linked to innovative projects.
• Development opportunities and a structured evolution plan.
• Integrate an innovative and globally renowned industrial company.
• Professional and stimulating challenges, as well as rewarding human contacts.
• A competitive salary package, in line with your experience.

Dunkerque LNG est en charge de l’exploitation et de la commercialisation du terminal méthanier de Dunkerque, deuxième plus grand terminal méthanier d’Europe continentale.

Fort d’un chiffre d’affaire annuel de 190€ millions, Dunkerque LNG est un atout majeur dans le développement de la stratégie d’approvisionnement en gaz du groupe EDF en raison de son raccordement unique à deux marchés de consommation : la France et la Belgique.

La société est composée d’une vingtaine de collaborateurs répartis sur les sites de Dunkerque et de Paris La Défense.

Afin de renforcer l’équipe commerciale de Dunkerque LNG à Paris, nous sommes activement à la recherche d’un (h/f) :

Ingénieur Commercial Grands Comptes

Responsabilités :

En tant qu’Ingénieur Commercial Grands Comptes, vous participez activement au développement du terminal tant d’un point de vue commercial qu’opérationnel. Rapportant au Directeur Commercial, vous êtes responsable de la relation commerciale avec les clients et les différents partenaires de Dunkerque LNG.

Vos principales responsabilités sont les suivantes :

• Entretenir et développer la relation commerciale avec les clients de Dunkerque LNG, EDF et Total.
• Veiller au respect des contrats de réservation de capacité et de leur mise en œuvre opérationnelle.
• Supporter la Direction Commerciale dans le pilotage de la relation contractuelle et/ou opérationnelle des prestataires : suivi du contrat de service, lancement et réception de nouveaux développements, etc.
• Prospecter de nouveaux clients, notamment en participant à différents forums et salons industriels.
• Planifier et gérer l’activité du terminal : bateaux, émission, stock, etc.
• Rapporter de manière régulière la performance commerciale et opérationnelle du terminal.
• Participer aux astreintes de soutien à raison d’une semaine sur quatre.

Profil :

• Vous êtes titulaire d’un Bac+5 de type école de commerce, d’ingénieur ou universitaire.
• Vous disposez de 10 ans d’expérience dans une fonction commerciale dans le secteur gazier.
• Vous êtes orienté(e) clientèle, résultats et solutions, et doté(e) d’un très bon relationnel.
• Vous êtes flexible, autonome, organisé(e), analytique et rigoureux(se).
• Vous communiquez aisément en Français et en Anglais.
• Vous êtes basé(e) à Paris La Défense et disposé(e) à vous déplacer de manière régulière à Dunkerque et ponctuellement à travers le monde.

Offre :

• Une fonction stimulante au sein d’un environnement diversifié.
• L’opportunité de rejoindre un acteur majeur dans l’industrie du gaz en Europe.
• Des challenges et des contacts variés au sein et en dehors de l’organisation.
• Des opportunités de développement et de formations.
• Un salaire attractif reprenant des avantages extra-légaux avantageux.

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.

Our client is one of the world’s leading and most-trusted suppliers to the pharmaceutical, biotech and specialty ingredients markets. They harnesse science and technology to create products that support safer and healthier living and that enhance the overall quality of life.

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

Team Leader – Quality Control

Cell Culture

You lead the QC team in a GMP environment on projects related to cell therapy and regenerative medicine. You manage the routine business of the Quality Control laboratory in accordance to GMP conditions. You lead and supervise all activities associated with their quality control stream and ensure all such relevant activities comply with all GMP and regulatory requirements.

Responsibilities:

• Ensure laboratory objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to customers.
• Support management in quality department planning and objectives.
• Schedule routine day-to-day laboratory operations and lab operation validation activities.
• Coordinate and supervise all analytical activities within the QC Laboratory ensuring all activities are carried out in a timely manner.
• Promote and support continuous improvement activities to position your team for future challenges.
• Oversee and develop a team of Quality Control Associate.

Profile:

• Bachelor’s or Master degree in Biotechnology, Biology or any related field.
• Minimum 5 years of experience in QC management positions with GMP standard in industrial environment.
• Experience with basic microbiological (gram stain, sterility), and/or analytical (RT-qPCR, FACS, ELISA) techniques.
• Strong leadership, project management and communication skills together with hands-on and pragmatic mind-set.
• Very good organizational, analytical and problem solving skills.
• Good proficiency in English.

Offer:

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

Our client is one of the world’s leading and most-trusted suppliers to the pharmaceutical, biotech and specialty ingredients markets. They harnesse science and technology to create products that support safer and healthier living and that enhance the overall quality of life.

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

Quality Assurance Officer

Cell Culture

You are responsible for planning and execution of daily quality assurance activities while ensuring compliance with international quality requirements as defined by the applicable guidelines (e.g. FDA, EMA, ICH) and all existing GMP standards in the area of responsibility.

Responsibilities:

• Plan and execute quality assurance activities (document management, batch records and label issuance, batch record review, equipment and supplier qualifications etc.) including documentation.
• Write, review and approve documentation (SOP’s, manufacturing and quality instructions, validation of protocols and reports, non-conformities, change requests).
• Monitor compliance with all applicable GMP and safety standards.
• Prepare data for trending (QRB, Annual Product Review) and support internal and external audits.
• Handle, distribute and archive controlled documents.
• Support the Qualified Person in his role, including audits and quality training.

Profile:

• Bachelor’s or Master degree in Biotechnology, Chemistry or any related field.
• 2 years of experience with GMP standard in industrial environment.
• Excellent technical writing, communication, and organizational skills.
• Proactive thinking team-player, accurate, attentive to detail, flexible, self-organized.
• Good proficiency in English.

Offer:

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