Offres d’emploi

Pharmacien d’Industrie

Responsabilités :

Rattaché(e) au Responsable du laboratoire, vous participez à l’ensemble des tâches liées à l’assurance qualité des activités du groupe.

Vos responsabilités principales sont de :

• Définir l’ensemble des flux : produits, personnel, matériel, consommable, déchets…
• Mener les analyses de risque relatives à l’ensemble des processus du laboratoire.
• Adapter et compléter le système documentaire aux exigences Eu GMP / BPF.
• Mener le PVD (Qualification locaux et équipements), avec le service qualité du groupe.
• Mettre en place le processus de vérification et de validation des rapports d’essais en conformité avec les exigences règlementaires.
• Intégrer les procédés, la qualité du produit et la sécurité du personnel dans la conception des bâtiments et des équipements.
• Auditer régulièrement le système en cours de mise en place afin d’en évaluer l’efficacité.
• Se tenir informé(e) des nouvelles règlementations
• Informer l’équipe du laboratoire des nouvelles règlementations.
• Maintenir à jour le système documentaire, les processus et les modes opératoires.
• Garantir la qualité au niveau des réalisations des processus.

Profil :

• Vous êtes Pharmacien d’Industrie.
• Vous disposez éventuellement d’une première expérience en industrie.
• Vous démontrez une passion pour l’assurance qualité et les environnements GMP.
• Vous êtes rigoureux/se, autonome, analytique, proactif/ve, et organisé(e).
• Vous êtes orienté(e) résultats, solutions, client et travail en équipe.
• Vous disposez d’une bonne connaissance des outils informatiques.
• Vous possédez une très bonne connaissance du français et de l’anglais. La connaissance du néerlandais est un atout.

Offre :

• Une fonction diversifiée comprenant de nombreuses responsabilités.
• L’opportunité de rejoindre une entreprise professionnelle et conviviale, et de contribuer à sa forte croissance.
• Des possibilités de formation, de développement et de coaching.
• Un contrat à temps plein et à durée indéterminée, assorti d’un package salarial adapté à votre profil et à votre niveau d’expérience.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

European Projects Manager – Green Technologies

Responsabilités :

En tant que European Projects Manager, vous coordonnez les projets européens dont GreenWin est partenaire. En outre, vous assurez la participation du pôle et de ses membres dans divers réseaux et groupes de travail européens.

• Coordonner les projets européens avec les partenaires industriels et académiques, et l’équipe du pôle.
• Prospecter et cartographier les acteurs de l’économie biosourcée en Wallonie.
• Transposer les projets européens au niveau régional et explorer les chaines de valeur qui peuvent être développées en Wallonie.
• Participer aux activités de communication sur les projets.
• Réaliser les rapports d’activité et reportings financiers des projets vers les institutions concernées.
• Représenter le pôle et ses membres au sein des réseaux et groupes de travail européens.
• Au sein de ces réseaux européens, identifier les appels à projets pour les membres du pôle et créer les synergies adéquates afin d’obtenir les financements européens et de lancer les projets.

 Profil :

• Vous disposez d’un diplôme d’Ingénieur, scientifique ou équivalent.
• Vous bénéficiez d’environ 5 ans d’expérience dans la gestion de projet d’innovation. Des connaissances en projets européens sont un atout.
• Vous démontrez un intérêt pour les technologies vertes : chimie, construction et environnement.
• Vous êtes un(e) excellent communicateur et disposez d’une réelle aisance relationnelle.
• Vous etes proactif(ve), pragmatique et orienté service. Vous faites également preuve d’un esprit d’équipe développé.
• Vous maîtrisez le français et avez de bonnes connaissances en anglais (niv.B2 minimum).

Offre:

• Une fonction variée au sein d’une équipe dynamique et d’une organisation au service du développement économique de la Wallonie.
• Un accompagnement vous permettant d’exprimer progressivement vos talents dans un contexte d’innovation.
• Un salaire attractif assorti d’avantages extra-légaux en phase avec votre expérience.
• Un contrat à durée indéterminée à temps plein.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Senior Project Leader – Preclinical Development

As a Sr Project Leader, you will report to the CEO and advance the company’s lead program from target validation through to preclinical development.

In a matrix organisation, your main responsibilities are as follows:

• Define, validate, implement and lead the program’s objectives, resources, and risks.
• Coordinate in-vitro/ex-vivo/in-vivo preclinical developments with external collaborators/providers.
• Report the program’s evolution to the stakeholders in a structured and detailed way.
• Manage the program from target validation to development.
• Manage scientific reporting for obtained grants and find new grant opportunities.
• Provide CSO/CEO with innovative R&D projects to develop product portfolio.
• Compile data, analyse, summarise and present results.

Profile:

• You are PhD with 5 to 10 years’ experience in cancer small molecules drugs preclinical development.
• You have experience with cell-based assays, in-vivo/ex-vivo pharmacology, including working knowledge of in-vivo PK, PD and efficacy studies.
• You show leadership in experimental design and data analysis.
• You demonstrate good understanding of in-vitro cellular and biochemical assays, including reporter assays, siRNA/shRNA knockdown, CRISPR-mediated genome editing & qPCR.
• You are rigorous, detail-oriented, autonomous, committed and flexible.
• You show excellent oral and written communication skills in English.
• You have strong team spirit and excellent interpersonal skills.

Offer:

• A challenging 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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Research Assistant – A-Mansia

Responsabilités:

En tant que Research Assistant, vous réalisez les tâches de logistique et de recherche, l’assistance et la réalisation de projets de recherche variés. Vous évoluez au sein d’une équipe pluridisciplinaire travaillant sur le développement de compléments alimentaires et de médicaments.

Vos principales responsabilités sont les suivantes :

• Élaborer, valider et exécuter des essais expérimentaux à l’aide de procédures opératoires normalisées.
• Analyser et rapporter les résultats expérimentaux au sein de l’équipe.
• Soutenir la mise en œuvre d’essais dans le cadre de plusieurs projets cibles.
• Collaborer avec les intervenants des projets et discuter des résultats d’analyse avec eux.
• Compiler des données, analyser, résumer et présenter des résultats expérimentaux.
• Rendre compte régulièrement de l’évolution de votre travail.

Profil:

• Vous êtes titulaire d’un Bachelier en Biotechnologie ou Technologue de laboratoire. Idéalement, vous possédez un Master en Sciences Biomédicales.
• Vous disposez de 2 à 5 ans d’expérience dans un environnement pharma ou biotech.
• Vous possédez de bonnes connaissances en biochimie, dosages enzymatiques et immunologiques, Elisa et Western Blot.
• Vous démontrez également de bonnes connaissances en culture cellulaire, biochimie immunohistochimie et moléculaire (PCR ; RT-PCR, Extraction ARN, ADN).
• Vous êtes doté(e) d’un bon esprit d’équipe et d’un esprit d’initiative et faites preuves de compétences organisationnelles développées.
• Vous êtes rigoureux(se), polyvalent(e), précis(e) et fiable.
• Vous maîtrisez les outils informatiques classiques, dont la suite Microsoft.
• Vous communiquez aisément en français (oral et écrit). La maîtrise de l’anglais est un plus.

Offre:

• Une fonction diversifiée au sein d’une jeune start-up en plein développement.
• L’opportunité de rejoindre un environnement à taille humaine, dynamique, innovant et professionnel.
• Un contrat à durée indéterminée à temps plein.
• Un package salarial attractif en phase avec votre expérience.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

(Senior) R&D Engineer

Responsibilities:

As a (Senior)-R&D Engineer, you lead and take care of designing, developing and testing the next generation of iStar implants and delivery systems, from the concept phase to human use. In collaboration with other team members, you identify innovative and reliable product designs. Reporting to the VP R&D, you play a key role in the R&D/innovation activities.

Your main responsibilities are:

• You conceptualize, design and develop the delivery systems, including design requirements, prototype developments, feasibility evaluations, pre-clinical and clinical assessments.
• You perform and document literature reviews to support customer requirements/design inputs identification, protocol design, pre-clinical studies.
• You support the development of new test methods, tooling and equipment procurement, and executing long term testing for the delivery tool.
• You manage R&D projects, within budget and agreed upon timelines
• You identify and manage suppliers to develop new products.
• You collaborate with colleagues and physicians in clinical developments in order to evaluate technology and to have a better understanding of ocular anatomy.
• You work with team members and external partners to deliver key technical objectives of the projects.
• You report results and work progress on a regular basis to the top management.
• You take ownership and responsibility for tasks assigned to you.

Profile:

• Mechanical or Biomedical Engineering Master’s degree, PhD is a plus but not required.
• Minimum of 5 years industrial experience in design, development, scale-up and commercialization of medical products.
• Experience in medical device design (implant and/or instruments), usability engineering and manufacturing is required.
• Understanding and knowledge of Design Control, familiar with FDA, GMP, QSR and ISO13485 requirements.
• 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. Another language is a plus.
• You are prone to travel worldwide up to 15% of your work time to support product development and clinical investigation trials.

Offer:

• A full-time permanent position within a high-potential medical device company with direct impact on the lives of patients.
• A professional, dynamic and stimulating work environment.
• A variety of interesting contacts with international exposure.
• An attractive compensation package in line with the position responsibilities and your experience.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Clinical Research Associate/Manager

Responsibilities:

Reporting to and working closely with the Chief Medical Officer, as Clinical Research Associate/Manager, you are responsible for the operational management and the oversight of clinical trials according to the clinical strategy.

Your main responsibilities are :

• Support and manage clinical trials for company, including protocol writing, clinical investigation reports, site selection and qualification of investigators.
• Facilitate and support physician training for initiation of the trial, Site Initiation Visits, patient enrollment according to protocol inclusion criteria and site monitoring.
• 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.
• Site monitoring, including scheduled visits, events reporting and documented interactions with clinical sites
• Compiles required clinical documentation for regulatory submissions including patient consent forms, contracts and monitoring plans.
• 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.
• Represent the company in all regulatory and third party audit requests for clinical trial information.
• Deal with product-related site request and solve issues.
• Engage with physicians and clinical staff, build relations and credibility to be a high level spokes partner.
• Create and maintain effective partnerships with KOL.
• 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.
• 4-7 years minimum in the management of pre- and post-market medical device studies (class III) at country or European level.
• Experience in clinical trial protocol writing, support for cardiovascular medical devices, and ability to manage 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.
• Excellent oral and written communication skills in English. Any other language is a plus.
• Up to 30% 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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Senior R&D Engineer – Catheter

Responsibilities:

As a Senior 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.
• 5 to 10 years experience in catheters design, development and industrialization within medical device companies.
• 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
• 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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Product Regulatory Affairs Specialist

Responsibilities:

As Product Regulatory Affairs Specialist, you are in charge of writing the technical documentation to support clinical study applications, CE marking and FDA registration. You insure compliance of product technical files with regulatory standards and provide support to ensure that regulatory standards are part of the Product Development Process.

Your main responsibilities are:

• Write technical documentation including Investigator Brochures, Clinical Protocols, Product Risk Analysis, Biocompatibility Risk Assessments.
• Prepare technical files for Clinical Studies filings, CE-Mark applications and FDA registrations.
• Maintain technical documentation to ensure compliance with internal QMS and Regulatory Standards.
• Support R&D and Manufacturing to define the product/process validation strategies in compliance with Regulatory Standards.
• Ensure that normative and regulatory changes are identified in a proactive manner and coordinate actions plans.
• Manage product registration processes.
• Report work evolution on a regular basis.

Profile:

• Master’s degree or Ph.D. degree in Science or equivalent through experience.
• About 3 years of experience supporting Regulatory Affairs for Class II & III Medical Devices.
• Strong technical writing skills (Investigator Brochures, Clinical Study Protocols, Risk Management).
• In-depth knowledge of regulatory requirements, MDR’s and EU ISO regulations and US FDA Quality System Regulations 21 CFR Part 820 and Part 11 (preferred).
• Excellent interpersonal, communication and presentation skills.
• High level of attention to detail, excellent organizational skills and time management, flexibility.
• Fluent in English, written and spoken. Knowledge of another language is an asset.
• Willing to travel abroad occasionally.

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

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Regulatory Affairs Manager

Responsibilities:

As Regulatory Affairs Manager, you are in charge of writing the technical documentation to support clinical study applications, CE marking and FDA registration. You insure compliance of product technical files with regulatory standards and provide support to ensure that regulatory standards are part of the Product Development Process.

Your main responsibilities are:

• Write technical documentation including Investigator Brochures, Clinical Protocols, Product Risk Analysis, Biocompatibility Risk Assessments.
• Prepare technical files for Clinical Studies filings, CE-Mark applications and FDA registrations.
• Maintain technical documentation to ensure compliance with internal QMS and Regulatory Standards.
• Support R&D and Manufacturing to define the product/process validation strategies in compliance with Regulatory Standards.
• Ensure that normative and regulatory changes are identified in a proactive manner and coordinate actions plans.
• Manage product registration processes.
• Report work evolution on a regular basis.

Profile:

• Master’s degree or Ph.D. degree in Science or equivalent through experience.
• 5 to 10 years’ experience in Regulatory Affairs for Class II & III Medical Devices.
• Strong technical writing skills (Investigator Brochures, Clinical Study Protocols, Risk Management).
• In-depth knowledge of regulatory requirements, MDR’s and EU ISO regulations and US FDA Quality System Regulations 21 CFR Part 820 and Part 11 (preferred).
• Excellent interpersonal, communication and presentation skills.
• High level of attention to detail, excellent organizational skills and time management, flexibility.
• Fluent in English, written and spoken. Knowledge of another language is an asset.
• Willing to travel abroad occasionally.

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

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Technicien
Peintures UV

Responsabilités :

En tant que Chimiste R&D, vous formulez des peintures photo-polymérisables (UV) adaptées aux supports plastiques pour développer la gamme de produits de DSCOLOR.

Vos responsabilités sont les suivantes :

• Développer et réaliser des formulations et nouvelles peintures photo-réticulables de DSCOLOR sur supports plastiques en laboratoire.
• Veiller à la qualification et validation des formulations en laboratoire selon les cahiers des charges de l’automobile et de la cosmétique.
• Réaliser les essais industriels, le scale-up et les validations sur le terrain (production).
• Prendre contact avec les fournisseurs de matières premières.
• Participer à différents salons de représentation.
• Rapporter l’évolution des démarches de manière régulière et structurée vers le responsable.

Profil :

• Vous disposez d’une forte expérience en formulation de peintures photo-réticulables (photo-polymérisation) sur des supports plastiques.
• Bonne connaissance des résines UV (uréthanes acrylates et polyesters acrylates) ainsi que des photoamorceurs UV pour systèmes pigmentés.
• Une expérience dans des systèmes 2K polyuréthanes est un plus.
• Expérience avérée dans le domaine des peintures pour pistolage industriel.
• Vous communiquez aisément en Français et disposez de bonnes connaissances en Anglais (oral et écrit).

Offre :

• Intégrer une entreprise reconnue internationalement et en pleine croissance.
• Une fonction challengeante avec un réel impact sur la société.
• Un salaire attractif accompagné d’une assurance hospitalisation et d’une assurance groupe.
• Un contrat à temps plein en CDI.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Laboratory Logistics Coordinator

Function :

Reporting to the Associate Director, Operations, the Laboratory Logistics Coordinator is responsible for the instrument logistics, biosafety, monitoring of instruments and facilities and overall management of laboratory area.

Tasks include :

• Scheduling and overseeing external maintenance and calibration of all instruments and equipments;
• Performing internal qualification of basic equipments (i.e. pipette calibration, balance calibration, thermal mapping of storage equipments);
• Ensuring that equipments are used, maintained and calibrated as per SOP;
• Ensuring that equipment log books are complete and properly maintained; ensuring that calibration reports are completed in a timely manner;
• Managing all instruments and equipment malfunctions and associated documentation as per SOP;
• Purchasing of new equipments (obtaining quotes, ensuring that IQ/OQ/PQ is performed and documented as per SOP);
• Management of the monitoring system for facilities and instruments;
• Ensuring laboratory areas are adequately maintained (planning of maintenance, repair, decontamination and cleaning of laboratory space);
• Managing Health and Biosafety for the site;
• Training laboratory personel on laboratory biosafety rules and equipment operations;
• Participating to the writing and review of laboratory equipment SOP;
• Ensuring that all above laboratory management activities are documented according to GDP procedures;
• Participating in client and/or regulatory agencies audits.

Profile of the applicant :

The applicant must hold a bachelor 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 in a similar position. Experience in working in a Quality environment is an asset.

The applicant must :

• Be meticulous, thorough and proactive;
• Demonstrate excellent organizational 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 (ISO15189, GCLP, GMP) and apply good documentation procedures (GDP).
• 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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Research Assistant – Flow Cytometry and Serology – Evenings and weekends

Function :

Reporting to the Associate Director, Operations 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. You will receive a strong training to further develop your skills in cellular and humoral immunology.

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;

Profile of the applicant :

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.  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.
• Must be able to work evenings and weekend hours.
• 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 of 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.
• Strong training and development opportunities.
• A competitive salary package including benefits (and premium for evenings and weekend hours), adapted to your experience and the context.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.