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Medical Director - Bio-Pharma/Biotech - Liège

Founded in April 2014 in Grenoble (France) as a spin-off of the French Blood Bank (Etablissement Français du Sang, EFS), PDC*line Pharma is a Belgian-French biotech company that is developing a novel class of off-the-shelf cancer immunotherapies based on a proprietary Plasmacytoid Dendritic Cell line (PDC*line) pre-loaded with peptides that are derived from target tumor antigens.

After a first-in-human feasibility clinical study in melanoma, PDC*line Pharma is focusing on lung cancer with a new candidate in phase 1b/2 clinical trial (PDC*lung) and neoantigens (PDC*Neo).  The company currently comprises f 20 people and has an experienced management team. In March 2019, PDC*line signed a licensing deal with a leading Korean pharmaceutical company for the development and commercialization of PDC*lung cancer vaccine for lung cancer. The total deal value is 108M€ (123M$) plus significant tiered royalties on net sales in Asia.

In order to strengthen the management team located in Liege, we are actively looking for a:

Medical Director

Responsibilities:

As a Medical Director, you are responsible for providing medical and scientific input into the Study Team and into the Project Teams. You are in charge of planning, designing, developing, executing and interpreting clinical studies. Your main responsibilities are:

  • Design clinical development plans, optimize and execute them efficiently and effectively.
  • Drive the selection of sites for clinical studies, identify investigators and opinion leaders.
  • Write or review study synopsis, protocols, reports and documents (g. CRF, ICF and TMF) for regulatory agencies.
  • Ensure medical monitoring of clinical studies.
  • Responsible in evaluating adverse events and handling safety information as appropriate, for the management of safety review boards, CROs and other vendors for study and/or safety-related issues.
  • Serve as the primary medical liaison to the investigators, opinion leaders, clinical leaders and medical teams of pharma partners.
  • Develop and maintain a network of medical experts in the field and represent PDC*Line in interactions with investigators, at meetings and conferences.
  • Provide direction on all clinical matters to the PDC*line teams.
  • Provide review and query of overall clinical data sets, clinical laboratory and author reports.
  • Participate in medical writing of regulatory documents (IND, briefing documents, etc).
  • Coordinate and oversee the execution of drug safety process. In collaboration with the clinical team and CRO, you are responsible for safety documentation for clinical trials.
  • Participate in the development plan strategy with the other members of management and in the R&D plan development lead by the CSO.
Profile:
  • Medical Degree (MD) with strong scientific background and medical practice experience, a fellowship or equivalent in (immuno-)oncology is a plus.
  • Experience in a pharmaceutical or biotech company, especially in early stage, exploratory clinical development of drugs and biologics.
  • At least 5 years’ experience in performing early development clinical activities and safety assessment activities.
  • At least 2 years of successful experience managing and directing a study or project team.
  • Working knowledge of GCP, ICH guidelines, EMA and FDA regulations.
  • Ability to work in a small, yet international environment with complex issues.
  • Excellent organizational, communication and interpersonal skills.
  • Effective time, cost and resource management skills.
  • Ability to lead and motivate personnel.
Offer:
  • An interesting position within a high-potential clinical stage biotech company.
  • The opportunity to work in a human-sized and multicultural team environment.
  • A variety of interesting contacts with international exposure.
  • An attractive salary package in line with the position responsibilities and your experience. 

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Senior Scientist - Bio-Pharma/Biotech - Mont-Saint-Guibert

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

Based in Mont-Saint-Guibert (30km from Brussels) and reinforced by its 21 million euros fundraising success, A-Mansia is searching for a dynamic and enthusiastic person to strengthen the team.

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

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

Senior Scientist

As a Senior Scientist, you report to the Head of Pharma Development and to the CEO in order to lead the company’s therapeutic protein development program(s) from preclinical to clinical stage. You are responsible for performing experiments and managing the project. You bring the company’s promising investigational product to clinical proof of concept by combining internal and external resources.

Your main responsibilities are as follows:
  • Lead the scientific program of the investigational product development by performing experiments.
  • Develop new processes to test in vitro the investigational product(s).
  • Coordinate in vivo preclinical experiments with external collaborators/providers/CROs.
  • Report results at R&D/Comex meetings.
  • Manage scientific reporting for obtained grants and find new grant opportunities.
  • Provide CSO/Head of Pharma with innovative R&D projects to develop product portfolio.
Profile:
  • You are Ph.D, Vet.D or M.D with at least 5 years of experience in pharma developments.
  • You have an experience and expertise in protein development as IMPD.
  • You are experienced with cell-based assays and in vivo experimentation
  • Knowledge of quality control processes and microbiota field would be a plus
  • Rigorous, detail-oriented, autonomous, committed and flexible.
  • Excellent oral and written communication skills in English and French.
  • 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 – Virology and Serology - Bio-Pharma/Biotech - Gosselies

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.

In the context of its growing immune monitoring service offering, Caprion is looking to hire a Research Assistant for its flow cytometry and serology platforms, for its site in Gosselies, Belgium.

Research Assistant – Virology and Serology

Function :

Reporting to the Associate Director, Operations and working closely with Principal Scientists, the Research Assistant, Virology and Serology, will work within a team focusing on the characterization of the cellular and of the humoral immune response. The main responsibilities will include the development and execution of viral neutralization assays, foci forming unit assays, Luminex and ELISA assays.

Tasks include :

  • Perform viral and other serological assays 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 Research Assistant Level 2 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 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. A minimum of three (3) years demonstrated experience in techniques related to virology and humoral immunology is required.

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.

CHIMISTE R&D Peintures UV - Industry - Lens-Saint-Servais

Basée à Lens-Saint-Servais, la société DSCOLOR est spécialisée dans le développement et la production de peintures décoratives uniques et innovantes sur plastique pour les secteurs de l’automobile et de la cosmétique.

Avec deux sites de production en Belgique et en Allemagne, la société utilise de réelles technologies innovantes telles que : Holoptique, MetaLazer, Holographique 3D, Chrome effect, Vernis UV dual cure, Vernis SoftFeel, Vernis Polyurethane et plus encore. DSCOLOR collabore avec de nombreux acteurs industriels reconnus comme : Dior, Nokia, BMW, Philips… La société a d’ailleurs été nominée aux Global Industrie Awards dans la catégorie « Nouvelle Technologie ».

Pour plus d’informations, veuillez visiter le site http://www.dscolor.com/

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

Chimiste R&D
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 êtes titulaire d’un Master/ Ingéniorat ou Doctorat en chimie ou équivalent par expérience.
  • Vous disposez d’une forte expérience en formulation de peintures photo-réticulables (photo-polymérisation) et UV DUAL CURE 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.

CMC Manager - Biotechnology - Gosselies

Minoryx is a clinical stage biotech company leading the development of new therapies for X-ALD and other rare diseases with a high unmet medical need. The company’s leading program is MIN-102, a novel, orally bioavailable and selective PPAR gamma agonist with a superior profile for central nervous system-related diseases. It is currently in an ongoing phase 2/3 clinical trial for the treatment of adrenomyeloneuropathy (AMN) in EU and US. The trial enrolls adult male patients affected by AMN, the most frequent phenotype of X-linked adrenoleukodystrophy (X-ALD), in Europe and the US, with results expected in 2020. Please visit http://www.minoryx.com/.

Minoryx is expanding its activities and potential indications for MIN-102 and is now launching a clinical trial in a second orphan CNS indication (Friedreich’s Ataxia). Recently the company opened a second R&D site at the i-Tech Incubator (Brussels South Biopark – Charleroi, Belgium). The company is backed by a syndicate of experienced investors and has support from a network of other organizations. Minoryx was founded in 2011 and has raised more than €50M, including a €21.3M Series B closed in September 2018.

Minoryx is actively looking for a candidate for the position of CMC manager (m/f). The candidate will be located in the Belgian subsidiary but would be expected to maintain close contact with the team located at the HQ in Mataró (Barcelona, Spain) and will be reporting to the Director of CMC. The position includes travels to visit CDMOs as needed.

CMC Manager

Responsibilities:

As a CMC Manager, you support day-to-day CMC internal and external activities in terms of process, technical expertise and operational trouble shooting. You coordinate CMC operations in collaboration with other departments and suppliers.

Your main responsibilities are:

  • Monitor in-house and external CMC activities.
  • Provide technical expertise for the drug substance (DS) synthesis and processability.
  • Support drug product (DP) technical and planning activities.
  • Attend both drug substance (DS) and drug product (DP) key productions.
  • Identify potential analytical, processing, stability and compliance issues. Troubleshooting.
  • Review certificate of analysis, batch records and other technical documents.
  • Participates in the regular communications with the CDMOs and technology providers, discussing data, planning.
  • Liaise with other departments to provide them the requested CMC information.
  • Support in writing and reviewing CMC sections of the IMPD.
Profile:
  • BSc or MSc degree in Chemistry. Knowledge of pharmaceutical technology will be a plus.
  • 3 -5 years CMC experience in small molecules, mainly in drug substance (DS).
  • Solid experience in analytical, manufacturing and GMP.
  • Good understanding of synthesis, process development and process transfers implementation.
  • Agility, rapid response to changes.
  • Ability to work autonomously and to collaborate with a group in a goal- and team-oriented setting.
  • Effective communication skills.
  • Fluency in English (written and spoken).
  • Prepared to travel to the Spanish site and the CDMO sites around 15% of your work time.
Offer:
  • An interesting position within a high-potential clinical stage biotech company.
  • The opportunity to work in a human-sized and multicultural team environment.
  • A variety of interesting contacts with international exposure.
  • An attractive salary package in line with the position responsibilities and your experience.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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

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

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

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

Head of Pharma Development

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

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

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

R&D Engineer - Biotechnology - Wavre

Founded in 2011 and currently employing 18 people, iSTAR Medical is a clinical-stage medical technology company that aims to provide leading patient care through the design, manufacturing and marketing of novel ophthalmic therapies.

iSTAR Medical develops innovative ophthalmic implants for patients with glaucoma. The ophthalmic implants are made from proprietary STAR® material, a technology from the University of Washington in Seattle (USA). For additional information about the company and the technology, please visit http://www.istarmed.com/

In order to support the development of the company, we are currently looking for a (m/f) :

R&D Engineer

Responsibilities:

As a 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 Operations/R&D Director, 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 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 project’s technical objectives.
  • You report results and work evolution on a regular basis to the top management.
Profile:
  • Mechanical or Biomedical Engineering Master’s degree.
  • Around 5 year’s experience in design, development and industrialization of medical products.
  • Experience in medical device design (implant and/or instruments), usability engineering and manufacturing is an asset.
  • Familiar with FDA, GMP, QSR and ISO13485 requirements is a plus.
  • 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.
  • 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.

Senior Project Manager - Medical Device - Liège

Founded in 2016, Oncoradiomics is an innovative and ambitious start-up based in Liège. Oncoradiomics‘s strategic goal is to « revolutionize precision medicine”, by applying advanced artificial intelligence to clinical imaging.

Oncoradiomics focuses on tailoring cancer care to the clinical, imaging, biological and genetic characteristics of an individual patient so that the best outcome can be achieved.

Oncoradiomics holds several international grants and patents and is continuously developing and connecting with leading industrial and academic players to advance healthcare and the life sciences.

For the expansion of the team in Liège and in order to manage key clients’ and internal R&D projects, we are looking for a (m/f):

Senior Project Manager

Responsibilities:

As a Senior Project Manager, you are responsible for the delivery of the projects. You coordinate people and processes to ensure that key customers’ projects are delivered on time and achieve the desired results. Regarding the R&D projects, you lead the team in order to meet strategic objectives and the company’s ambition.

Reporting to the CEO, you lead the innovation throughout the company. Your main responsibilities are:

  • You monitor multiple projects from initiation through delivery and ensure that all projects are delivered on time, within scope and budget.
  • You identify and clarify key projects requirements and customers’ needs, along with scientists, regulatory, sales and management expectations.
  • You work with key stakeholders and with the CEO to understand requirements, address business and system issues, in order to ensure that strategic goals are met.
  • You maintain schedules, track key milestones and program interdependencies and preempt risks.
  • You resolve conflicts in a timely manner to ensure that projects stay on track.
  • You oversee and manage the operational aspects of ongoing projects and serve as liaison between program management, planning and scientists’ team.
  • You review status of projects and budgets; you report results and work evolution on a regular basis to the top management.
Profile:
  • Bachelor’s or Master’s degree in IT, Engineering, Business, Mathematics or equivalent through experience.
  • Min. 7 years of experience in a project management position with technical products. Experience within a research environment or in medical imaging software and/or devices is a plus.
  • Experience with managing data solution, platform projects and AI technologies.
  • Experience in a Medical device or regulated industry and exposure to regulatory submissions. Understanding of FDA regulations including ISO 13485.
  • Project management methodology and Agile/Scrum Master certification are an asset.
  • Results and customer oriented, rigorous, structured, autonomous and flexible.
  • Analytical, organized, team player, open-minded with a start-up mind-set.
  • Strong transversal leadership and communication skills.
  • Perfect command in spoken and written French and English. Any other language is an asset.
  • Willing to travel for short periods, up to 20% of your time.
Offer:
  • A challenging and diversified position within a high-potential innovative start-up company.
  • To work in a dynamic, respectful and professional
  • International exposure, with learning and development opportunities.
  • An attractive compensation package in line with the position responsibilities and your experience.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Laboratory Logistics Coordinator - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences, a contract research organisation with facilities in Montreal (Canada), Gosselies (Belgium) and Freemont (USA), offers analytical services to biopharmaceutical companies for the characterization of the human immune response in pre-clinical and clinical samples.

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

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

Laboratory Logistics Coordinator

Function :

Reporting to the Associate Director, Operations, the Laboratory 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 – - Bio-Pharma/Biotech - Gosselies

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.

In the context of its growing immune monitoring service offering, Caprion is looking to hire a Research Assistant for its flow cytometry and serology platforms, for its site in Gosselies, Belgium.

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.

Pharmacien d’Industrie (QP) - Bio-Pharma/Biotech - Woluwé-Saint-Lambert

Située à Woluwe-Saint-Lambert, ß+ Pharma est une société spécialisée dans la production de radio-isotopes innovants à usage médical et destinés au diagnostic de maladies oncologiques, cardiologiques et neurologiques. Sa production couvre les besoins de ses clients sur le territoire du BeNeLux et une partie de la France.

Fondée en 2002 et composée de 11 collaborateurs, ß+ Pharma offre un environnement dynamique et un réel esprit d’équipe permettant l’épanouissement de tous ses employés.

ß+ Pharma fait partie du groupe Curium Pharma.

Afin de contribuer au développement de ß+ Pharma, nous sommes activement à la recherche d’un (h/f):

Pharmacien d’Industrie (QP)

Responsabilités:

En tant que Personne Qualifiée Adjointe, vous supervisez la production des radio-pharmaceutiques dans le respect des normes GMP et vous assurez la libération des lots. Vous rapportez directement à la Personne Qualifié Principale.

Vos principales tâches sont :

  • Libérer les lots produits en veillant à respecter les délais et les normes de qualité.
  • Participer aux activités de fabrication des radio-pharmaceutiques.
  • Gérer le système de qualité en accord avec les normes GMP.
  • Assurer le bon fonctionnement des activités de maintenance, de qualification, de validation et d’approvisionnement du service.
  • Participer à la formation initiale et continue du personnel.
  • Participer aux audits fournisseurs ainsi qu’aux audits sur les autres sites de production européens.
Profil:
  • Vous disposez d’un Master en Pharmacie, d’un Master complémentaire en Pharmacie Industrielle ainsi que d’un numéro QP.
  • Vous possédez une expérience avérée dans le domaine en industrie (radio-/bio-) pharmaceutique. Les candidatures sortant fraichement des études sont également les bienvenues.
  • Vous êtes respectueux(se), digne de confiance et aimez le travail en équipe.
  • Vous êtes flexible et faites preuve de rigueur.
  • Vous êtes dynamique et proactif(ve) et disposez de bonnes capacités de communication.
  • Vous maitrisez l’anglais et le français à l’oral comme à l’écrit.
Offre:
  • Une fonction diversifiée au sein d’une société en développement.
  • L’opportunité de rejoindre un environnement à taille humaine, dynamique et professionnel.
  • Un parcours de formation dès l’entrée en fonction et tout au long de votre évolution.
  • Un contrat à durée indéterminé assorti d’un package salarial attractif.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Clinical Trial Manager - Biotechnology - Gosselies

Minoryx (www.minoryx.com/) is a clinical stage biotech company leading the development of new therapies for rare diseases affecting the central nervous system. The company is backed by strong international investors.

The company’s leading program is currently in an ongoing phase II/III clinical trial in EU and US, with results expected in 2020. In the upcoming months, Minoryx is planning to launch a clinical trial for a second orphan indication.

Founded in Spain, Minoryx is opening a subsidiary in Gosselies (Belgium). In order to strengthen the team in Belgium, we are currently looking for a (m/f):

Clinical Trial Manager

Responsibilities:

Reporting directly to the Director of Clinical Operations and working closely with the team in Spain, you are responsible for the operational management and the oversight of clinical trials according to the clinical strategy.

Your main responsibilities are:

  • Coordinate clinical trial in collaboration with selected CRO.
  • Visit clinical study sites regularly and interact with study members.
  • Ensure successful execution of the clinical trials on time and on budget.
  • Review study related documentation and materials.
  • Co-monitor clinical study for protocol adherence and safety with selected CRO.
  • Ensure that clinical trial activities are documented in accordance with regulatory requirement.
  • Create and maintain effective relationships with KOL.
  • Report results and work evolution on a regular basis to the Director of Clinical Operations.
Profile:
  • Master’s or bachelor’s degree in Life Science or equivalent through experience.
  • At least 5 years of relevant experience in clinical trials.
  • Extensive knowledge of all aspects of GCP and regulations.
  • Track record on managing clinical studies on time & on budget.
  • Good collaboration, documentation and presentation skills.
  • Flexibility, good time management, team-working skills, stress resistant, ability to work proactively and independently.
  • Well-developed communication skills, problem solving skills, creative and critical thinking.
  • Excellent command of Microsoft Office Tools (Excel, Word, PowerPoint).
  • Fluent in English. A good command of French or Catalan is an asset.
  • Prepared to travel to Spanish site regularly, clinical investigational sites, conferences and meeting with regulators.
Offer:
  • An interesting position within a high-potential clinical stage biotech company.
  • The opportunity to work in a human-sized and multicultural team environment.
  • A variety of interesting contacts with international exposure.
  • An attractive salary package in line with the position responsibilities and your experience.

Interested ?

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

Principal Scientist - Bio-Pharma/Biotech - Gosselies

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.

Nous traitons votre candidature rapidement et de manière strictement confidentielle.

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

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

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

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

Research Assistant – Flow Cytometry and Serology

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.

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