Jobs

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

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

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

Pour renforcer l’équipe, 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.

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.
• 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 English. The command of French or 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.

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.

ASIT Biotech is a Belgian clinical-stage biotech company focused on the development of breakthrough immunotherapy products for the treatment of allergies.

Thanks to its innovative technology platform, ASIT Biotech currently holds a leading and unique position on the market. This innovation results in a short treatment, expected to improve patient compliance and quality of life. ASIT Biotech’s product pipeline targets to significantly expand the current immunotherapy market. For more information about the company, please vist www.asitbiotech.com.

With a headcount of 25 staff members, ASIT Biotech is located in Liège, Belgium. In order to support its high-potential developments, we are looking for a (m/f):

Head of Regulatory Affairs

Responsibilities:

As a Head of RA, you lead and drive the execution of ASIT global regulatory and quality assurance strategy. Reporting to the CEO, you are responsible for regulatory affairs, quality assurance, and compliance activities across the company. You define and implement the quality and regulatory policies in line with applicable directives, guidelines and legal requirements.

Your main responsibilities are as follows:

• Develop, propose and implement the company regulatory & quality strategy.
• Manage regulatory documents submissions for clinical studies, and product approvals.
• Implement an efficient quality system and a continuous improvement culture within the company.
• Interact with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, and follow-up of
submissions.
• Support and advise project teams on regulatory and quality issues.
• Provide technical review of data and reports for regulatory submissions.
• Draft product labelling, instruction leaflets and packaging.
• Participate in internal/external audits, inspections and provide post-inspection
follow-up.
• Write and update SOP, work instructions, and policies.

Profile:

• Master or PhD in life sciences or equivalent through experience.
• 10 years experience in a RA and/or a QA management position in the Biotech/Pharma sector.
• Track record in developing quality systems from EU/US clinical developments to product approval.
• Thorough knowledge of ICH guidelines, GxP and related regulatory guidances.
• Proven track record of building strong relationships with internal and external stakeholders.
• Ability to maintain multiple projects and meet timelines, including change management skills.
• Client-centered and solution-oriented, with hands-on and pragmatic mindset.
• Excellent leadership, communication and interpersonal skills.
• Familiar with MS Office solutions.
• Fluency in English.

Offer:

• A challenging leading position within a stimulating and dynamic work environment.
• A variety of interesting contacts with international exposure.
• The opportunity to have direct impact on the results of a high-potential biotech company.
• An attractive compensation package in line with the position responsibilities and your experience.

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

Responsibilities :

Reporting to the Laboratory Manager and working closely with Principal Scientists, the Research Assistant will 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.

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 :

The applicant must 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 and demonstrate a relevant laboratory experience. Theoretical and practical knowledge of techniques related to cellular and humoral immunology is required. Experience in cell culture and handling infectious materials in BL2+ environment is an asset.

The applicant must :

• Demonstrate excellent organisational skills.
• Demonstrate schedule adaptability and flexibility.
• Be willing to actively participate to the generation, the implementation and the continuous improvement of laboratory processes.
• Be willing to work in a Quality environment (ISO17025, GCLP, GMP) and apply good documentation procedures (GDP).
• Be functional in French (spoken and written) and have a functional knowledge of written English. Knowledge spoken English is an asset.

Offer :

• Full time permanent contract, with possibility of rapid start.
• Diversified tasks and responsibilities and interesting projects.
• A professional, dynamic and stimulating work environment.
• Training and development opportunities.
• A competitive salary package including benefits, adapted to your experience and the context.

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

For its site in Gosselies and in the context of its growing immune monitoring service offering, Caprion is looking for a (m/f) :

Principal Scientist

Responsibilities :

Reporting to the Director of Scientific Operations and working closely with the laboratory personnel, the Principal Scientist will work within a team focusing on the characterization of the cellular and humoral immune response, using various types of assays such as flow cytometry (phenotypic, ICS, etc) ELISPOT, ELISA, Luminex and viral neutralization tests.

Responsibilities include:

• Overseeing experimental design of flow cytometry, ELISPOT and antibody-based assays through generation of study-specific workplans and supporting documentation
• Acting as a key resource to provide guidance and support in root cause analysis and impact assessment
• Overall conduct of studies in different immune-therapeutic areas, acting as primary contact to the client for communication of study progress
• Data interpretation, report generation and presentation of results to clients

Profile :

The applicant must hold a doctorate degree in life science, with strong knowledge of immunology, with post-doctoral experience (or equivalent) and have a deep expertise of flow cytometry analysis. The applicant must also have a minimum of two years of experience in the industry.

The applicant must :

• Be proficient with analysis software such as FlowJo, Pestle, Spice, Prism and Excel and be able to perform complex analysis of flow cytometry data such as Boolean analysis.
• Demonstrate excellent communication and organisational skills.
• Be abreast of latest immune monitoring methodologies
• Have an excellent knowledge and understanding of GCLP regulations and other regulatory guidelines sufficient to carry out GCLP studies.
• Be willing to work in a Quality environment (ISO17025, GCLP, GMP) and apply good documentation practices (GDP).
• Be fluent in English (written & spoken) and able to functionally communicate in French.

Offer :

• Full time permanent contract.
• Diversified tasks and responsibilities and interesting projects.
• A professional, dynamic and stimulating work environment.
• Development opportunities.
• A competitive salary package including benefits, adapted to your experience and the context.

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.

Under the implementation plan in the Walloon Brabant province, its future development and reinforced by a 21 million euros fundraising success, A-MANSIA is looking 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, a few hours from European Capitals.

To strengthen the team in Mont-Saint-Guibert, we’re looking for an (m/f):

Chief Operating Officer

Main responsibilities:

Reporting directly to the CEO and as part of the executive committee, you are in charge of the whole operations management for the fermentation process starting from the sourcing of raw materials to the commercialisation of finished products. You are the point of contact with the CMO(s) in charge of the outsourced manufacturing of microbial products.

Your main tasks are:

• Lead production projects and product launch on the market: sourcing of raw materials with the CMO, logistic, galenic development & packaging.
• Coordinate with R&D and marketing departments to oversee the whole operation process.
• Coordinate the whole outsourced production and supply chain.
• Be part of the COMEX and report to Board of Directors on the strategic development of operations.
• Define specifications, negotiate contracts and manage the collaboration with CMOs and third parties.
• Ensure raw materials compliance and control outsourced performances.
• Control and lead the Cog’s at the product launch and on a long-term basis.
• Manage the internal supply chain team.

Profile:

• You hold a Ph.D. or you are engineer in Nutrition or Life Sciences, or equivalent through experience.
• You have at least 10 years of industrial experience in production management related to the production of probiotics/food complements.
• You have experience in and knowledge of fermentation processes.
• You have hands on experience in or knowledge of CMO and third parties management.
• You show strong leadership skills combined with a strategic and hands-on approach.
• You are skilled in project management related to food complements launch on the market.
• You take advantages of an extended network in the industry.
• You are rigorous, flexible, hands-on, independent, dynamic and pro-active.
• You are fluent in English. The command of French and/or Dutch is an asset.

Offer :

• A diversified executive position within a high-potential start-up company.
• A key position for the development of the company.
• The opportunity to join a human sized, dynamic and professional environment.
• A permanent employment contract.
• An attractive compensation package in line with your experience.

Located in Gosselies (Belgium), MaSTherCell is a service company (CDMO) in biotechnology. MaSTherCell is specialized in production outsourcing, process development and quality management (QA/QC/QP) for cell therapy.

With around 140 employees, MaSTherCell supports its customers (big pharma, biotech, etc.) in the development and production of innovative medicines. MaSTherCell actively contributes to improving the quality of life and health of many patients. For more information, please visit http://www.masthercell.com.

To support MaSTherCell in its strong growth, we are actively looking for a (m/f):

Program Management Officer

Responsibilities:

Reporting to the Executive committee, you assist them in selecting and planning strategic internal projects/programs (including new sites integration), and in reporting on their progress.

Your main responsibilities are:

• You implement project management tools, project control processes, procedures and policies.
• You monitor and control the internal program/project throughout their entire lifecycle.
• You select program/project and you argue program/project closedown if necessary.
• You assess the relative priority of internal projects and programs.
• You set up performance reporting and program/project governance for customer and internal projects.
• You lead the project financial tracking with the business controller.
• You provide support to project teams and task planning.
• You report your work on a regular basis.

 Profile:

• Master’s degree or equivalent through experience.
• Minimum 5 years experience in a project management officer position.
• A project management professional certification is an asset.
• Strong 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.
• Good oral and written communication skills in English. Any other language is a plus.
• Computer skills:  Microsoft office, Digital document management system and Project management IT tools.

Offer:

• A challenging and diversified position within a high-potential innovative biotech company.
• To work in a human size, dynamic, respectful and professional environment.
• A variety of interesting contacts with international exposure.
• An attractive compensation package in line with the position responsibilities and your experience.

Dunkerque LNG (Dunkerque Liquefied Gaz Naturel) est une filiale à 65 % du groupe EDF SA, 25 % de l’opérateur belge Fluxys et 10 % de Total. L’exploitant du terminal méthanier de Dunkerque est Gaz-OPALE, filiale d’exploitation de Dunkerque LNG.

GAZ-OPALE est en charge de la conduite, de la maintenance et du respect des exigences HSE (Hygiène Sécurité et Environnement). Le terminal méthanier est un site ICPE (Installation Classée pour la Protection de l’Environnement) qui suit la directive SEVESO III seuil haut.

Responsable QHSE

Responsabilités :

En tant que Responsable QHSE, votre mission est de définir et coordonner la politique «qualité, hygiène, sécurité et environnement» de l’ensemble du terminal méthanier. Pour ce faire, vous pouvez compter sur une équipe de 2 personnes et sur un réseau de partenaires externes. Rapportant au Directeur d’Exploitation, vous faites partie du Comité de Direction de Dunkerque LNG.

Vos principales responsabilités sont les suivantes :

• Implémenter et coordonner le système de gestion de la sécurité : élaboration des plans d’urgence et mise en œuvre d’exercices.
• Coordonner la sécurité du site, gérer et analyser les événements et incidents.
• Évaluer et sensibiliser aux risques des postes de travail.
• Participer au Comité d’Hygiène, de Sécurité et des Conditions de Travail (CHSCT).
• Obtenir la triple certification Iso 9001, 14001, OHSAS 18001 par la mise en œuvre de documents contrôlés.
• Garantir la mise en œuvre des évolutions réglementaires et assurer la gestion des déchets.
• Veiller à la bonne application des règles d’accès au site.
• Participer aux astreintes de la cellule de crise opérationnelle à raison d’une semaine sur cinq.

Profil :

• Vous êtes titulaire d’un Bac+5 QHSE, scientifique, ou équivalent par expérience.
• Vous possédez une expérience réussie de 5 à 10 ans en tant que Responsable QHSE d’un site industriel type SEVESO. Une première expérience en management est un plus.
• Vous communiquez aisément en français et en anglais.
• Vous êtes autonome, rigoureux(se) et faites preuve d’un esprit d’ouverture, d’écoute et de synthèse.
• Vous appréciez le travail d’équipe et possédez une grande aisance relationnelle.
• Vous êtes habitué(e) à travailler dans un environnement structuré et exigeant (ISO 9001-14001, OHSAS 18001).
• Vous êtes basé(e) dans les environs de Dunkerque et êtes disposé(e) à vous déplacer ponctuellement en France et à l’étranger (Bruxelles, Zeebrugge, etc.)

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.

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):

Junior Product Specialist

Responsibilities:

As a Junior 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. In order to take on these responsibilities successfully, you’ll benefit from broad training and individual coaching.

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.
• report work evolution on a regular basis.

Profile:

• Master’s degree in Business, Engineering or equivalent through experience.
• Ideally first level experience in Product Management. Experience in medical software and/or devices is a plus. Experience in nutrition is also an asset. New graduates are also welcome.
• Results and customer oriented, rigorous, autonomous and flexible.
• Analytical, organized, team player, open-minded with a start-up mind-set.
• Fluent in English. The command of French or 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.
• Coaching and training path adapted to your needs.
• An attractive salary package and evolution opportunities.