If you are passionate about science, strive for new challenges in a fast-pace environment, and ready to work in a highly collaborative organization, join CellCarta and help shape the future of precision medicine.
We are a leading global CRO laboratory with headquarters in Canada. Our mission is to map precision medicine by providing comprehensive testing solutions and biomarker research to the top global pharmaceuticals and biotech companies. We are committed to providing superior science through proactive partnerships with our clients.
More than your traditional CRO, we have a scientist-to-scientist approach and our culture is one of flexibility, accessibility, and service excellence. We are looking for science enthusiasts driven by innovation and eager to join a diversified team of scientists.
At CellCarta we are committed to giving our team the very best. Join us as we continue to expand internationally and be part of the future of precision medicine.
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Location: Montreal , Quebec
The Quality Control Reviewer incumbent will perform quality control activities which are relevant to his/her field of expertise and linked to assigned projects.
Key Responsibilities
Education
Required Experience and Skills
Location: Montreal , Quebec
Le technicien de contrôle qualité est chargé d’effectuer une variété de tâches liées au contrôle de la qualité.
Principales Responsabilités
Éducation
Expérience et compétences requises
Location: Montreal , Quebec
Summary
Reporting to the Assistant Controller, the Accountant - Accounts Payable is responsible for supporting the accounts payable process from receipt of invoices to payment. The Accountant - Accounts Payable controls expenses by receiving, verifying, processing and reconciling invoices with the purchase orders and receiving slips. The ideal candidate enjoys working in a friendly atmosphere, has a good attention to detail and has strong organizational skills.
Main Responsibilities
Education
Main Requirements
Location: Montreal , Quebec
Résumé du poste
Relevant du contrôleur adjoint, le comptable, comptes créditeurs est responsable du soutien des processus des comptes créditeurs depuis la réception des factures jusqu’au paiement. Le candidat (la candidate) contrôle les dépenses (réception, vérification, traitement et rapprochement des factures) avec les bons de commande et les bordereaux de réception. Le candidat (la candidate) idéal(e) aime travailler dans une atmosphère conviviale, possède un souci du détail et de solides compétences organisationnelles.
Responsabilités principales
Formation
Exigences principales
Location: Greater Boston Area , MA
Summary
CellCarta is looking for a digital marketing specialist to help grow its businesses and client base. Reporting to the Marketing Director, you will lead and execute all digital campaigns using marketing automation and CRM tools. The ideal candidate is a self-starter and strives on delivering business results while continuously improving. If you are dynamic and creative and can coordinate deliverables in a fast-pace environment in a rapidly growing industry, this role is for you. As a member of the Sales Operations and Marketing team, you will also help educate and support our internal teams on new digital advertising/marketing platforms initiatives and provide support to the marketing team on various campaigns and advertisements initiatives to promote breakthrough work in the CRO industry.
Main Responsibilities
• Work closely with the Marketing Director and Scientific Content Specialist to develop and execute all digital campaigns
• Lead our marketing automation efforts, manage the execution of B2B digital campaigns to achieve CellCarta’s key objectives using Salesforce and PARDOT
• Support and execute B2B digital media campaigns (SEM/SEO, Paid Social & Display, Email Marketing and Social Medias) to increase web traffic and lead generation
• Develop and maintain campaign architecture in PARDOT for various business scenarios
• Use automation to plan and execute PARDOT drip campaigns to support our lead nurturing strategy
• Create and manage automation workflows and segment lists to tailor campaigns for targeted audiences across specific market segments
• Analyze and report campaign performance; develop A/B test plans to improve response.
• Collaborate with marketing team to develop and maintain a global campaign calendar
• Develop unique creative digital content in various formats (videos, animated gif, banners, infographics) and ability to edit content with calls to action that drives engagement
• Responsible for the development, maintenance, and improvements of the corporate website, and provide recommendations to improve customer journey
• Report on key campaign metrics, including creating ad hoc and monthly reports
• Perform campaign management tasks as needed
Qualifications and Requirements
• Bachelor’s degree in Marketing, Digital Marketing or relevant field
• Minimum of 2-4 yrs of experience in a full time B2B digital /inbound marketing role
• Expert Pardot/Salesforce user
• Experience in creating and executing multiple campaigns with understanding of customer journey (understanding of the drug development process is an asset)
• Knowledge of the pharmaceutical industry and CRO industry, a strong asset
• Strong experience in executing and analyzing SEO/SEM, display/paid media, social media (LinkedIN, Facebook, Instagram, Twitter, YouTube, Vimeo) and email marketing campaigns
• Strong expertise in web development project management experience, CMS experience (WordPress and other CMS)
• Well versed in data analytics (e.g., Google Analytics, Google Search Console, SEMRush etc.)
• Google Analytics Certification and Google Ads Certification a plus
• Advanced HTML/CSS knowledge
• Strong expertise with Adobe Creative Suite/Creative Cloud – Photoshop, Illustrator, InDesign
Skills
• Ability to take direction with minimal supervision, work independently and is a positive team player
• Track record of strong execution and delivery of commitments
• Ability to write, edit and adapt compelling content for digital channels (an asset)
• Strong attention to detail and ability to respond to situations quickly
• Strong analytical and project management skills
• Excellent verbal and written communication skills
Location: Montreal , Quebec
Sommaire du poste
Caprion est à la recherche d’un scientifique très motivé et enthousiaste possédant une solide formation et une expérience pratique dans le domaine des immunoessais (MSD et ELISA). Le candidat ou la candidate jouera un rôle essentiel dans l'analyse d'échantillons d’une variété de fluides biologiques et d'échantillons d'étude de tissus en suivant les procédures normalisées d’exploitation (PNE) et les bonnes pratiques de laboratoire (BPL). Il ou elle devra également procéder à l'optimisation/qualification et à la validation des méthodes.
Responsabilités principales
Compétences et expérience requises
Location: Montreal , Quebec
Position Summary
The Data Analyst performs a variety of analytic functions within the CellCarta Precision Medicine Inc. Flow Cytometry Department. These functions include analysis and reporting of flow cytometry data and data from other platforms as needed. The analyst works under the supervision of the Associate Director of the Data Analysis Unit to ensure accurate and timely completion of data analysis. Maintains study-related documentation as per GLP/GCLP and regulatory guidance.
The position requires to be available two weekends per month, from Wednesday to Sunday on the day shift
Key Responsibilities
Education
M.Sc. or PhD in immunology.
Required Expertise and Skills
Location: Montréal , Québec
Sommaire
L’analyste de données en immunologie occupe différentes fonctions au sein du département d'analyse de données. C’est fonctions incluent l’analyse et la production de rapports concernant les données en cytométrie en flux et de données provenant de d’autres plateformes. Le titulaire du poste se doit de maintenir la documentation en lien avec les différentes études à jour, selon les normes réglementaires tel que GLP/GCLP. Finalement, l’analyste de données relèvera de la directrice adjointe de l’unité d’analyse.
Principales Responsabilités
Éducation
Expérience
Location: Montreal , Quebec
Sommaire du poste
CellCarta recrute un(e) technicien(ne) expérimenté(e) et qualifié(e) en logistique d’échantillons pour travailler en étroite collaboration avec les équipes opérationnelles sur la logistique et le suivi des envois internationaux liés à des essais cliniques.
Principales responsabilités
Formation
Principales exigences du poste
Location: Montreal , Quebec
Position Summary
CellCarta is seeking a Sample Logistics Technician to work closely with the Operations teams for the logistics and tracking of international clinical trial shipments.
Main Responsibilities
Education
Main Requirements
Location: Montreal , Quebec
Conseiller juridique
Relevant du vice-président des affaires juridiques, du conseiller juridique et du secrétaire général, le conseiller juridique joue un rôle stratégique en soutenant 1) la croissance de l’entreprise en donnant une variété de conseils sur diverses questions juridiques et réglementaires en rapport avec les initiatives de croissance stratégique ; et 2) les activités quotidiennes et les opérations mondiales dans divers secteurs juridiques. Le conseiller juridique joue également un rôle essentiel dans la structuration et le développement de cette nouvelle fonction juridique.
Si vous êtes un joueur d’équipe motivé et que vous possédez une formation en droit commercial et un sens aigu des affaires, cette l’occasion est pour vous!
Responsabilités
Exigences
___________________________
Legal Counsel
Reporting to the VP Legal Affairs, General Counsel & Corporate Secretary, as Legal Counsel, you will play a strategic role in supporting 1) growth of the business by advising on various legal and regulatory matters in connection with strategic growth initiatives; and 2) day-to-day activities and global operations in various areas of laws. The Legal Counsel will also be instrumental in structuring and growing this new legal function.
If you are a motivated team player with a commercial legal background and a keen business sense, this is the perfect opportunity for you!
Responsibilities
Requirements
Location: Montreal , Quebec
Caprion Biosciences Inc. is a leading clinical research organization (CRO) laboratory in immune monitoring, protein characterization and tissue pathology solutions for immunotherapy and drug development. Located in Montreal, California, Chicago, Belgium, UK, Australia and soon in China. Employees at Caprion are true scientific partners working together to enhance people’s health and quality of life.
SUMMARY
Caprion is seeking a highly motivated and enthusiastic Scientist with strong background and hands-on experience n immunoassays (MSD and ELISA). This individual will play a key role in analyzing samples on a variety of biological fluids and tissue study samples following Standard Operating Procedures (SOP) and Good Laboratory Practices (GLP). He will also be required to perform method optimization/qualification and validation.
MAIN RESPONSIBILITIES
EDUCATION
EXPERIENCE AND SKILLS REQUIRED
Location: Montreal , Quebec
Position Summary
Reporting to the Group Leader, the incumbent will work within a team dedicated to the characterization of cellular ( various flow cytometry assays such as PBMC phenotyping, and the detection of intracellular cytokines, etc.) and humoral (ELISA tests, Luminex, viral neutralization tests, etc.) response.
Main responsibilities:
Required skills and experience
Work conditions
Rotating schedules between evening and weekend shifts:
-Evening: Monday to Friday, from 1:00 pm to 9:00 pm
-Weekend: Wednesday to Friday, from 1:00 pm to 9:00 pm AND Saturday to Sunday, from 9:00 am to 5:00 pm
Location: Montréal , Québec
Sommaire du poste
Se rapportant au gestionnaire de laboratoire, le titulaire du poste travaillera au sein d’une équipe dédiée à la caractérisation de la réponse immunitaire cellulaire (ELISPOT et essais de cytométrie en flux variés tels que phenotypage de PBMC, et la détection de cytokines intracellulaires, etc) et humorale (tests ELISA, Luminex, tests de neutralisation virale, etc.).
Horaire: Mercredi au Vendredi de 13h à 21h et le samedi et dimanche de 9 à 17h
Principales responsabilités
Compétences et expérience requises
Location: Montreal , Quebec
Laboratory Technician
Summary
The laboratory technician provides support in experiment preparation (solutions, consumables, labels) and in samples and solution preparation. He participates in the maintenance and upkeep of equipment, in the reception of reagent and material, and inventories. The laboratory technician is working in a GLP environment.
Main Responsibilities
• Performs sample preparation such as cell isolation from blood sample, cryopreservation, thawing, counting;
• Provides general support in experiment preparation such as plastic identification and labels preparation;
• Prepares solutions and reagent aliquots;
• Performs equipment maintenance, calibration, and cleaning;
• Replenishes stocks materials and perform inventories;
• Performs files archiving.
Education
• DEC in Laboratory Technology, preferably with a biotechnology specialization.
Main Requirements
• 1-year experience in laboratory;
• Experience in working with a biological safety cabinet using sterile conditions;
• Experience in working with PBMC (isolation by Ficoll or CPT, cryopreservation, thawing, counting with hemocytometer);
• Experience in a GLP/GCLP environment an asset;
• Organized and rigorous in the conduct of their work;
• Good record keeping skills and attention to detail;
• Dynamic, and motivated.
Location: Montreal , Quebec
Technicien de laboratoire
Sommaire du poste
Le technicien de laboratoire fournit un soutien dans la préparation d’expériences (solutions, consommables, étiquettes) et dans la préparation d’échantillons et de solutions. Il/elle effectuera des expériences en laboratoire conformément aux méthodes PON. Les tâches supplémentaires comprendront également (mais sans s’y limiter) l’entretien, la maintenance des équipements, la réception des réactifs et du matériel, ainsi que l’inventaire. Le technologiste médical travaillera dans un environnement BPL et CAP/CLIA.
Principales responsabilités
• Prépare les échantillons selon différentes techniques: isolation cellulaire à partir d’échantillons sanguin, comptage, décongélation, cryopréservation;
• Apporte un support général dans la préparation des expériences tel que l’identification des plastiques et la préparation des étiquettes;
• Prépare les solutions et les aliquotes de réactifs;
• Fait la maintenance, la calibration et le nettoyage des équipements;
• S’assure de remplir les stocks lorsque vide et fait l’inventaire;
• S’occupe de l’archivage.
Formation requise
• DEC en Technique de laboratoire, d’analyse biomédicale ou équivalent.
Compétences et expérience requises
• 1 an d’expérience en laboratoire;
• Expérience de travail avec une armoire de sécurité biologique dans des conditions stériles;
• Expérience de travail avec les PBMC (isolement par Ficoll ou CPT, cryoconservation, décongélation, comptage avec hémocytomètre);
• Expérience dans un environnement BPL/GCLP, un atout;
• Être organisé et rigoureux dans son travail;
• Capacité à bien documenter son travail et souci du détail;
• Dynamique, et motivé.
Location: Wilrijk , Antwerpen
As a global Research Organization to the biopharmaceutical industry, CellCarta (formerly Caprion – HistoGeneX) provides access to a broad offering of biomarker platforms and services. We partner with our clients to address the most complex scientific testing needs, delivering customized biomarker testing solutions to further the limitless potential of precision medicine.
We offer our services on a global scale through our laboratories in USA, Canada, Belgium, China and Australia. Combining expertise in histopathology, immune monitoring, proteomics, genomics and sample logistics, we support pharmaceutical and biotechnology companies in the research and development of innovative new medicines for the treatment of cancer and immune diseases. Working under stringent quality and regulatory requirements, we strive to make a difference in the future treatment options offered to patients.
CellCarta leverages its strong expertise in cancer to support the entire spectrum of biomarker services including biomarker discovery in the research phase, tumor profiling and biomarker monitoring in clinical studies and companion diagnostics registration studies, patient diagnostics and development of new techniques and tests for tumor analysis and prediction of treatment response. The company bridges the gap between research, clinical studies and diagnostics.
We are currently recruiting a Business/technical IT Analyst (Software implementation)
Department: IT
Based in
Wilrijk, Antwerp (Belgium)
Function
We are looking for a Business/technical IT Analyst (Software implementation) who will focus on translating the needs from the operational teams to requirements for the LIMS development team. This role will play a crucial part in the build out of our company’s LIMS system.
Major responsibilities
Background
What we can offer
Location: Wilrijk , Antwerpen
As a global Research Organization to the biopharmaceutical industry, CellCarta (formerly Caprion – HistoGeneX) provides access to a broad offering of biomarker platforms and services. We partner with our clients to address the most complex scientific testing needs, delivering customized biomarker testing solutions to further the limitless potential of precision medicine.
We offer our services on a global scale through our laboratories in USA, Canada, Belgium, China and Australia. Combining expertise in histopathology, immune monitoring, proteomics, genomics and sample logistics, we support pharmaceutical and biotechnology companies in the research and development of innovative new medicines for the treatment of cancer and immune diseases. Working under stringent quality and regulatory requirements, we strive to make a difference in the future treatment options offered to patients.
CellCarta leverages its strong expertise in cancer to support the entire spectrum of biomarker services including biomarker discovery in the research phase, tumor profiling and biomarker monitoring in clinical studies and companion diagnostics registration studies, patient diagnostics and development of new techniques and tests for tumor analysis and prediction of treatment response. The company bridges the gap between research, clinical studies and diagnostics.
We are currently recruiting a Quality Assurance Manager
Department: Quality Assurance
Based in
Wilrijk, Antwerp (Belgium)
Function
The QA Manager works as member of the Quality Assurance team, ensuring that all activities are performed in accordance with GCP, GCLP, CAP/CLIA and ISO15189.
Major Responsibilities
• Assist in defining quality procedures in conjunction with the operational teams (SOPs, forms, work instructions, policies)
• Assist in administrative duties related to the QA section
• Perform internal audits
• Participate in sponsor audits and regulatory inspections (preparation, hosting and follow-up actions)
• Participate in review of non-conformities, deviations and complaints and support to related investigations
• Participate to the CAPA review process
• Work with relevant departments to ensure timely closure of quality action plans
• Actively contribute to continuous improvement and quality awareness initiatives
• Contribute to the implementation of new quality standards (ISO13485)
• Ensure registration of QA related training
• Contribute to the preparation of management reviews
• Assist in the follow-up of KPI’s
• Contribute actively in the risk management activities of the company
Background
• Bachelor or Master Degree in life sciences with preferably 3 years of experience in a quality assurance role in a laboratory or an IVD manufacturing environment
• Advanced knowledge, orally and in writing of English, knowledge of Dutch and French is a plus
• Excellent organizational skills
• Dynamic personality, a true team player with good interpersonal skills
• Analytical thinker with a process-oriented mindset
• Ability to work independently
• Good documentation skills (accurate, attention to details)
• Experience related to quality and regulatory aspects of in vitro diagnostic devices (ISO13485, IVDD, IVDR and/or FDA IDE and PMA regulations) is an advantage
• Willingness to travel
What can we offer
• A dynamic and rapidly changing global environment allowing personal growth
• A company that is fit for the future
• A competitive salary and benefits
• A great team you can work with
Location:
As a global Research Organization to the biopharmaceutical industry, CellCarta (formerly Caprion – HistoGeneX) provides access to a broad offering of biomarker platforms and services. We partner with our clients to address the most complex scientific testing needs, delivering customized biomarker testing solutions to further the limitless potential of precision medicine.
We offer our services on a global scale through our laboratories in USA, Canada, Belgium, China and Australia. Combining expertise in histopathology, immune monitoring, proteomics, genomics and sample logistics, we support pharmaceutical and biotechnology companies in the research and development of innovative new medicines for the treatment of cancer and immune diseases. Working under stringent quality and regulatory requirements, we strive to make a difference in the future treatment options offered to patients.
CellCarta leverages its strong expertise in cancer to support the entire spectrum of biomarker services including biomarker discovery in the research phase, tumor profiling and biomarker monitoring in clinical studies and companion diagnostics registration studies, patient diagnostics and development of new techniques and tests for tumor analysis and prediction of treatment response. The company bridges the gap between research, clinical studies and diagnostics.
We are currently recruiting an IT Senior Director MSP Governance Validation & Lab End User Support
Department: IT
Based in
Preferably Naperville (US). Alternatively Montréal (Canada) or Wilrijk, Antwerp (Belgium)
Major responsibilities
Background
What can we offer
Location: Wilrijk , Antwerpen
Als globale onderzoeksorganisatie in de biofarmaceutische industrie, voorziet CellCarta (Vroeger: Caprion – Histogenex) toegang tot een breed aanbod van biomarker platforms en services. Wij werken samen met onze partners om de meest complexe wetenschappelijke testen uit te voeren. Zo leveren we persoonlijke biomarker oplossingen om steeds verder te gaan in de eindeloze mogelijkheden van precieze medicatie.
Wij bieden onze services op globale schaal aan via onze laboratoria in de US, Canada, België, China en Australië, waar we expertise hebben op vlak van histopathology, immune monitoring, proteomics, genomics en sample logistics. Wij ondersteunen farmaceutische en biotechnische bedrijven in het onderzoek en de ontwikkeling van nieuwe innovatieve medicatie voor de behandeling van kanker en immuniteitsziektes.
Werkend onder strenge kwaliteit en wettelijke vereisten, streven wij ernaar om een verschil te maken in de toekomstige behandelingen die we aan patiënten kunnen bieden.
CellCarta maakt gebruik van zijn sterkte ervaring in kankeronderzoek om het hele spectrum te ondersteunen van biomarker services, inclusief biomarker ontdekking in de onderzoeksfase, tumor profilering en biomarker monitoring in klinische studies en registratiestudies voor begeleidende diagnostiek, patiënten diagnoses en de ontwikkeling van nieuwe technieken en testen voor tumor analyses en de voorspelling van behandelingsrespons. Het bedrijf is de brug tussen onderzoek, klinische studies en diagnoses.
Momenteel zijn we op zoek naar een Laboratorium Technoloog (m/v) om ons team te versterken.
Departement: IHC en FISH waar de immuno-histochemische en fluorescente in situ hybridisatie technieken worden toegepast.
Gebaseerd in
Wirlijk, Antwerpen (Belgie)
Belangrijkste taken (Na een interne opleiding zal je worden ingezet voor)
• het uitvoeren van gespecialiseerde immunohistochemische en fluorescente kleuringen, en in situ hybridisatie analyses en dit zowel manueel als op verschillende automatische kleurtoestellen
• de controle over de werking van de toestellen en het signaleren van storingen
• het opvolgen van de laboprocessen en de registratie van gegevens in het labo informatiemanagementsysteem (LIMS)
• de documentatie van het uitgevoerde labowerk
• het assisteren bij de data interpretatie
Profiel
• Je heb een diploma Professionele bachelor (Medische, Farmaceutische of Biomedische laboratorium technologie of Biochemie)
• Voorafgaande ervaring in een laboratorium is een pluspunt • Je kan vlot met de computer overweg (Word, Excel)
• Ervaring met een LIMS systeem is mooi meegenomen
• Je bent flexibel, communicatief en werkt graag in teamverband
• Basiskennis Engels is noodzakelijk
• Je zal werken binnen een ISO kwaliteitssysteem, wat vereist dat je nauwkeurig en gedocumenteerd kan werken
Aanbod
• Contract van onbepaalde duur
• Tijdregeling: Voltijds
• Dienstregeling: Dagwerk
• Je komt in een dynamisch groeiend bedrijf terecht waar we werken volgens de 38 uren werkweek
• Om de woon/werk balans in evenwicht te helpen houden geven we je, boven het wettelijk verlof, nog extra vakantiedagen
• Je krijgt een competitief loon en extralegale voordelen
Location:
As a global Research Organization to the biopharmaceutical industry, CellCarta (formerly Caprion – HistoGeneX) provides access to a broad offering of biomarker platforms and services. We partner with our clients to address the most complex scientific testing needs, delivering customized biomarker testing solutions to further the limitless potential of precision medicine.
We offer our services on a global scale through our laboratories in USA, Canada, Belgium, China and Australia. Combining expertise in histopathology, immune monitoring, proteomics, genomics and sample logistics, we support pharmaceutical and biotechnology companies in the research and development of innovative new medicines for the treatment of cancer and immune diseases. Working under stringent quality and regulatory requirements, we strive to make a difference in the future treatment options offered to patients.
CellCarta leverages its strong expertise in cancer to support the entire spectrum of biomarker services including biomarker discovery in the research phase, tumor profiling and biomarker monitoring in clinical studies and companion diagnostics registration studies, patient diagnostics and development of new techniques and tests for tumor analysis and prediction of treatment response. The company bridges the gap between research, clinical studies and diagnostics.
We are currently recruiting an IT Manager Security
Department: IT
Based in
Global role - Preferably Wilrijk, Antwerp (Belgium) or Montréal (Canada)
Major responsibilities
Background
What can we offer
Location: Wilrijk , Antwerpen
As a global Research Organization to the biopharmaceutical industry, CellCarta ( formerly Caprion – HistoGeneX) provides access to a broad offering of biomarker platforms and services. We partner with our clients to address the most complex scientific testing needs, delivering customized biomarker testing solutions to further the limitless potential of precision medicine.
We offer our services on a global scale through our laboratories in USA, Canada, Belgium, China and Australia. Combining expertise in histopathology, immune monitoring, proteomics, genomics and sample logistics, we support pharmaceutical and biotechnology companies in the research and development of innovative new medicines for the treatment of cancer and immune diseases. Working under stringent quality and regulatory requirements, we strive to make a difference in the future treatment options offered to patients.
CellCarta leverages its strong expertise in cancer to support the entire spectrum of biomarker services including biomarker discovery in the research phase, tumor profiling and biomarker monitoring in clinical studies and companion diagnostics registration studies, patient diagnostics and development of new techniques and tests for tumor analysis and prediction of treatment response. The company bridges the gap between research, clinical studies and diagnostics.
We are currently recruiting an IT Manager Data Reporting & Analysis
Department: IT
Based in
Wilrijk, Antwerp (Belgium)
Major responsibilities
Background
What can we offer
Location: Montreal , Quebec
Sommaire du poste
Caprion est actuellement à la recherche d’un technicien(ne) chevronné(e) de la gestion des échantillons pour travailler en étroite collaboration avec les équipes des Opérations à, recevoir et gérer les échantillons ainsi que les réactifs et le matériel.
Principales Responsabilités
Formation
Exigences principales
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Position Summary
Caprion is seeking a Sample Management Technician to work closely with the Operations teams, receiving and managing samples as well as reagents and materials.
Main Responsibilities
Education
Main Requirements
Location: Montreal , Quebec
Sommaire
Relevant du gestionnaire aux approvisionnements, le spécialiste aux approvisionnements est responsable des achats de matériels et réactifs de laboratoire. Le spécialiste examine les demandes afin de valider les besoins de matériels et réactifs, prépare les commandes et calculs les coûts. Il aide aux inventaires et fait le suivi des commandes afin de s’assurer de recevoir la marchandise commandée dans les délais requis.
Responsabilités
Formation Académique
Expérience et Compétences
_________________________________
Summary
Reporting to the Procurement Manager, the Procurement Specialist is responsible for purchasing laboratory supplies and reagents. The Procurement Specialist reviews purchase requests to validate the needs for reagents and laboratory supplies, prepares the orders and establishes costs. The Procurement Specialist will assist in managing inventories levels as determined by the needs of the business. This individual will be responsible for follow ups with all vendors to ensure orders are received in a timely fashion.
Responsibilities
Education
Experience and skills
Location: Chicago , IL
Summary
The Associate Director of Supplier Quality is responsible for developing and deploying quality processes and systems associated with managing suppliers. This involves developing policies, processes, procedures and systems for approving and maintaining an approved list of qualified suppliers.
Responsibilities
Education
Requirements
Location: Montreal , Quebec
Sommaire du poste
Caprion est à la recherche d'un gestionnaire de programme afin d'organiser et de coordonner les programmes scientifiques. Le gestionnaire de programme fournit aux équipes et aux scientifiques principaux une orientation stratégique afin de les aligner sur les objectifs de l'entreprise.
Principales Responsabilités
Éducation
Exigences Requises
--------------------------------------------------------------------------------------------------------------------------------------
Position Summary
Caprion is seeking a Program Manager to organize and coordinate scientific programs. The Program Manager provides strategic guidance to teams and Principal Scientists to align with the company’s objectives.
Main Responsibilities
Education
MSc in life science
Main Requirements
Location: Wilrijk , Antwerpen
Als globale onderzoeksorganisatie in de biofarmaceutische industrie, voorziet CellCarta (Vroeger: Caprion – Histogenex) toegang tot een breed aanbod van biomarker platforms en services. Wij werken samen met onze partners om de meest complexe wetenschappelijke testen uit te voeren. Zo leveren we persoonlijke biomarker oplossingen om steeds verder te gaan in de eindeloze mogelijkheden van precieze medicatie.
Wij bieden onze services op globale schaal aan via onze laboratoria in de US, Canada, België, China en Australië, waar we expertise hebben op vlak van histopathology, immune monitoring, proteomics, genomics en sample logistics. Wij ondersteunen farmaceutische en biotechnische bedrijven in het onderzoek en de ontwikkeling van nieuwe innovatieve medicatie voor de behandeling van kanker en immuniteitsziektes.
Werkend onder strenge kwaliteit en wettelijke vereisten, streven wij ernaar om een verschil te maken in de toekomstige behandelingen die we aan patiënten kunnen bieden.
CellCarta maakt gebruik van zijn sterkte ervaring in kankeronderzoek om het hele spectrum te ondersteunen van biomarker services, inclusief biomarker ontdekking in de onderzoeksfase, tumor profilering en biomarker monitoring in klinische studies en registratiestudies voor begeleidende diagnostiek, patiënten diagnoses en de ontwikkeling van nieuwe technieken en testen voor tumor analyses en de voorspelling van behandelingsrespons. Het bedrijf is de brug tussen onderzoek, klinische studies en diagnoses.
Momenteel zijn we op zoek naar een Biosample Operator om ons team te versterken.
Departement: Bio Sample Management
Gebaseerd in
Wirlijk, Antwerpen (Belgie)
Functie
Wij hebben voor jou de unieke mogelijkheid om als schoolverlater of laborant(e) met ervaring bij ons aan de slag te gaan in de afdeling ‘Biosample Management’. Binnenkomende stalen worden geregistreerd in het 'Labo informatie management systeem', verplaatst van en naar hun bewaarlocaties en terug gestuurd naar de klant na analyse. Je werk hier is dus de basis waarop andere teams hun moleculaire en immunohistochemische technieken gaan toepassen. Daarnaast wordt ook onderzoek gedaan naar de verschillende parameters die de kwaliteit van de weefselstalen beïnvloeden. Je begrijpt dat dit werk cruciaal is om achteraf correcte en zo goed mogelijke analyseresultaten te kunnen produceren.
Profiel
• Voorafgaande ervaring in een laboratorium of een studie Medisch Secretariaat is een pluspunt maar geen vereiste
• Je kan vlot met de computer overweg (Word, Excel) en met een database of je bent bereid dit te leren
• Je bent communicatief en werkt graag in teamverband
• Je zal werken binnen een kwaliteitssysteem (ISO 15189:2012), wat vereist dat je nauwkeurig en gedocumenteerd werkt
Jobgerelateerde competenties
• De stalen ontvangen en controleren: De datum, het tijdstip van de afname, de gegevens van de persoon met een zorgbehoefte, ... registreren
• Administratie en documentenbeheer uitvoeren
• Werkplaats en materiaal desinfecteren, ordelijk en net houden. Het afval afvoeren/vernietigen
Persoonsgebonden competenties
• Leervermogen hebben
• Samenwerken als hecht team
• Zich kunnen aanpassen aan veranderende omstandigheden (flexibiliteit)
• Omgaan met stress
• Klantgerichtheid
• Plannen (= ordenen)
• Zelfstandig werken
• Contactvaardig zijn
• Zin voor nauwkeurigheid hebben
• Creatief denken (Inventiviteit)
• Regels en afspraken nakomen
Aanbod
• Contract van onbepaalde duur
• Tijdregeling: Voltijds
• Dienstregeling: Dagwerk
• Je komt in een dynamisch groeiend bedrijf terecht waar we werken volgens de 38 uren
werkweek
• Je zal deel uitmaken van een snel groeiend en innovatief bedrijf met goede
doorgroeimogelijkheden
• Om de woon/werk balans in evenwicht te helpen houden geven we je, boven het wettelijk
verlof, nog extra vakantiedagen
• Je krijgt een competitief loon en extralegale voordelen
Location: Wilrijk , Antwerpen
Als globale onderzoeksorganisatie in de biofarmaceutische industrie, voorziet CellCarta (Vroeger: Caprion – Histogenex) toegang tot een breed aanbod van biomarker platforms en services. Wij werken samen met onze partners om de meest complexe wetenschappelijke testen uit te voeren. Zo leveren we persoonlijke biomarker oplossingen om steeds verder te gaan in de eindeloze mogelijkheden van precieze medicatie.
Wij bieden onze services op globale schaal aan via onze laboratoria in de US, Canada, België, China en Australië, waar we expertise hebben op vlak van histopathology, immune monitoring, proteomics, genomics en sample logistics. Wij ondersteunen farmaceutische en biotechnische bedrijven in het onderzoek en de ontwikkeling van nieuwe innovatieve medicatie voor de behandeling van kanker en immuniteitsziektes.
Werkend onder strenge kwaliteit en wettelijke vereisten, streven wij ernaar om een verschil te maken in de toekomstige behandelingen die we aan patiënten kunnen bieden.
CellCarta maakt gebruik van zijn sterkte ervaring in kankeronderzoek om het hele spectrum te ondersteunen van biomarker services, inclusief biomarker ontdekking in de onderzoeksfase, tumor profilering en biomarker monitoring in klinische studies en registratiestudies voor begeleidende diagnostiek, patiënten diagnoses en de ontwikkeling van nieuwe technieken en testen voor tumor analyses en de voorspelling van behandelingsrespons. Het bedrijf is de brug tussen onderzoek, klinische studies en diagnoses.
Momenteel zijn we op zoek naar een Laboratorium Technoloog Pre Analytische fase om ons team te versterken.
Departement: Pre Analytics
Gebaseerd in
Wirlijk, Antwerpen (Belgie)
Functie
In de sectie ‘Pre-Analytische fase’ kunnen we een paar extra handen gebruiken. Hier worden binnenkomende stalen van verschillende oorsprong verwerkt die dan verder gekleurd en geanalyseerd worden in onze andere units. Je werk is dus de basis waarop andere teams hun moleculaire en immunohistochemische technieken gaan toepassen. Daarnaast wordt ook onderzoek gedaan naar de verschillende parameters die de kwaliteit van de stalen beïnvloeden. Je begrijpt dat dit een cruciale fase is om achteraf zo goed mogelijke analyseresultaten te kunnen produceren. We werken voornamelijk in het kader van klinische studies waarmee we onze bijdrage trachten te leveren in de ontsluiering van het kankerproces.
Profiel
· Voorafgaande ervaring in een laboratorium is een pluspunt; Voorafgaande ervaring met microtomie is een groot pluspunt
· Je kan vlot met de computer overweg (Word, Excel) en met een (LIMS-) database of je bent bereid dit te leren
· Je bent communicatief en werkt graag in teamverband
· Je zal werken binnen een kwaliteitssysteem (ISO 15189:2012), wat vereist dat je nauwkeurig en gedocumenteerd werkt
· Kandidaten gelijkwaardig in ervaring komen ook in aanmerking voor deze vacature
Jobgerelateerde competenties
· Talenkennis: NEDERLANDS (zeer goed) ENGELS (in beperkte mate)
· Werkervaring: beperkte ervaring
Persoonsgebonden competenties
· werkinstructies volgen
· bereid zijn tot leren
· nauwkeurig werken
· samenwerken
Aanbod
· Contract van onbepaalde duur
· Tijdregeling: Voltijds
· Dienstregeling: Dagwerk
· Je komt in een dynamisch groeiend bedrijf terecht waar we werken volgens de 38 uren werkweek
· Om de woon/werk balans in evenwicht te helpen houden geven we je, boven het wettelijk verlof, nog extra vakantiedagen
· Je krijgt een competitief loon en extralegale voordelen
Location: Fremont , CA
Summary
Supports drug discovery across the biotechnology industry by performing complex cellular assay services on samples from patients, healthy donors, and various animal species. Most assays involve analyzing immune cells by flow cytometry to evaluate pre-clinical therapeutics, biomarkers, or drug activity in patients. Primarily involves hands-on laboratory work and documenting protocols, with additional time spent planning experiments, analyzing data, and presenting results as experience is gained.
Responsibilities
Education
Experience and Skills
Location: Montreal , Quebec
Summary
The Manager of the Flow Cytometry is responsible for ensuring that appropriate and efficient systems and procedures for the flow cytometry platform are in place and followed. The incumbent is the technical resources for flow cytometry instruments and data acquisition. Acts as technical resource for laboratory and scientific team using the flow cytometry platform. Manages the day-to-day activities of the cytometry unit. Implements new technologies to ensure the cutting-edge advantage of CellCarta is maintained
Main Responsibilities
Education
Main Requirements
Location: Montreal , Quebec
Summary
The R&D Product Manager is responsible for the management of the global R&D project portfolio, which includes the development and evaluation of new R&D project proposals, management of active projects, coordination with external and internal collaborators, as well as post-mortem analyses and lifecycle management for completed projects. The position will report to the Vice-President, R&D.
Principal Responsibilities
Education
Experience and Skills Required
Location: Montreal , Quebec
English description to follow
Sommaire du poste
CellCarta est à la recherche d’un spécialiste LIMS pour travailler en étroite collaboration avec le scientifique d’application LIMS avec l’objectif de mettre en œuvre de nouvelles études et de transférer les études existantes dans un nouveau LIMS.
Responsabilités principales
Compétences et expérience requises
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Position Summary
CellCarta is seeking a LIMS Specialist to work closely with the LIMS Application Scientist, helping to implement new studies and transfer existing studies into a new LIMS.
Main Responsibilities
Required skills and experience
Location: Fremont , CA
Position Summary
Caprion is seeking a Program Manager to organize and coordinate scientific programs. The Program Manager provides strategic guidance to teams and Principal Scientists to align with the company’s objectives.
Main Responsibilities
Education
Main Requirements
Location: Montréal , Québec
Sommaire du poste
Sous la gestion de la chef d’équipe, le titulaire du poste préparera les billes et fera les compensations des expériences dans le logiciel et assurera la mise en marche et la vérification des cytomètres de la plateforme selon les procédures en vigueur.
Ce poste est un travail de fin de semaine du mercredi au dimanche de 9h à 17h.
Principales responsabilités
Formation Requise
Expérience et compétences requises
Location: Montreal , Quebec
Le formateur est responsable de : a) la formation du personnel sur les méthodes spécifiques, les pratiques de travail, la documentation et les procédures Caprion, b) la formation sur le site clinique par l’intermédiaire de webinaires et de formation sur place, c) la fourniture de renseignements et de commentaires sur le rendement du personnel et les possibilités d’amélioration, d) la révision et la mise à jour des procédures opérationnelles normalisées (PON) selon les besoins, et e) le développement et le maintien du programme de formation selon les procédures établies par Caprion.
Responsabilités principales
Formation
Expérience et compétences
Conditions spéciales du poste actuel
Location: Fremont , CA
Position Summary
Reporting to the Director of Quality Assurance, the QA Manager has the overall responsibility for maintaining as well at enhancing the Quality Systems and providing support for standardization of procedures within the company for the assigned site/s in collaboration with QA Management. The position will oversee and manage Quality Assurance activities, ensuring GLP, GCP, Quality Processes, Training and Qualification. She/he is also responsible for conducting and or scheduling internal (Facility, Study-Specific) and hosting external audits to assess compliance with regulations, and company procedures. In addition, she/he will serve as the Quality/GxP resource for supporting project teams at the assigned site/s in collaboration with QA Management.
Main Responsibilities
Required Expertise and Skills
Location: Montreal , Quebec
Position Summary
Reporting to the Laboratory Manager (Global Services team), you will be responsible for performing and/or managing tasks related to equipment maintenance and management of laboratory equipment.
Key Responsibilities
Education
Experience
Knowledge and Skills
Location: Montreal , Quebec
Sommaire
Sous la gestion de la Gestionnaire de Laboratoire (équipe des Services Globaux), le titulaire du poste sera responsable d’exécuter et/ou de superviser des tâches liées à la maintenance et à la gestion des équipements de laboratoire.
Principales Responsabilités
Éducation
Expérience
Connaissances et aptitudes
Location: Montreal , Quebec
Position Summary:
Reporting to the Manager, Proposal Development, the Proposal Specialist will be responsible for assisting Business Development and Proposal Development teams with the preparation of budget estimates for service proposals, as well as answering RFPs/RFIs. The Quotation Specialist will work closely with the scientific, operations, and business development functional groups.
Key Responsibilities:
Education:
Experience:
Knowledge and Skills:
Location: Montréal , Québec
Caprion Biosciences est une entreprise globale en recherches contractuelles ayant des installations au Canada, en Belgique, aux États-Unis, en Angleterre, en Australie et en Chine. L’entreprise opère au niveau international et offre des services analytiques aux entreprises biopharmaceutiques.
Sommaire
Le spécialiste en propositions travaille étroitement avec les équipes des Ventes, Finance, Scientifiques et Approvisionnements, ainsi qu’avec les autres membres de l’équipe de préparation des soumissions afin de s’assurer que les soumissions de services de spectrométrie de masse soient générées à temps et selon les standards attendus. Le spécialiste en propositions est aussi responsable de la gestion et de la coordination des réponses aux demandes d’information (RFI) au niveau global.
Responsabilités
Formation Académique
Expérience et Compétences
Conditions de travail
Location: Montreal , Quebec
Summary
The Principal Scientist is responsible for the overall conduct of studies in different immune-therapeutic area, overseeing experimental testing design, as well as formulating conclusions and recommendations for next steps. The incumbent has the ability to present CellCarta capabilities to clients in a compelling way demonstrating value and differentiation as support function to Business Development activities as well as presentation of results to Sponsor and scientific meetings. The incumbent is ensuring that the timelines and milestones of a study are met by proactively assessing foreseeing challenges, assessing impact of deviations and overall quality of the study conduct.
Main Responsibilities
Education
Experience and Skills Required
Location: Montreal , Quebec
POSITION SUMMARY
The trainer is responsible for: a) training new staff on work practices, documentation and Caprion procedures b) monitor the laboratory work and documentation of the personnel, c) ensure that personnel have completed their documentation appropriately, d) bring support to team members as needed, e) provide input on improvement opportunities, f) review and update general SOPs as needed, and g) develop and maintain the training program at Caprion.
RESPONSIBILITIES
EDUCATION
REQUIREMENTS
Location: Gosselies
Position Summary:
The Laboratory Group Leader at Caprion is accountable for daily management of laboratory Research Assistants. In this role, he/she is responsible for scheduling laboratory work for all ongoing studies. The Laboratory Group Leader ensures that staff is appropriately trained and proficient with all techniques used and follows up on staff performance. The Laboratory Group Leader also monitors the quality of laboratory work and documentation to ensure compliance with applicable requirements.
Responsabilities:
Special Conditions of the Current Position:
Profile:
Knowledge Requirements:
Skill Requirements
Location: Gosselies
Résumé de la position:
Le chef de groupe de laboratoire de Caprion est responsable de la gestion quotidienne des assistants de recherche de laboratoire. Dans ce rôle, il / elle est responsable de la planification des travaux de laboratoire pour toutes les études en cours. Le chef du groupe de laboratoire s'assure que le personnel est correctement formé et compétent avec toutes les techniques utilisées et assure le suivi des performances du personnel. Le chef de groupe de laboratoire surveille également la qualité du travail et de la documentation du laboratoire pour garantir la conformité aux exigences applicables.
Responsabilités:
Conditions spéciales de la position:
Profil:
Connaissances requises:
Compétences requises:
Le masculin est utilisé par facilité.
Location: Pyrmont , Sydney
More than your traditional CRO, we have a scientist-to-scientist approach and our culture is one of flexibility, accessibility, and service excellence. We are looking for science enthusiasts driven by innovation and eager to join a diversified team of scientists.
At CellCarta we are committed to giving our team the very best. Join us as we continue to expand internationally and be part of the future of precision medicine.
Summary
The Principal Scientist is responsible for the overall conduct of studies in different immune-therapeutic area, overseeing experimental testing design, as well as formulating conclusions and recommendations for next steps. The incumbent has the ability to present CellCarta capabilities to clients in a compelling way demonstrating value and differentiation as support function to Business Development activities as well as presentation of results to Sponsor and scientific meetings. The incumbent is ensuring that the timelines and milestones of a study are met by proactively assessing foreseeing challenges, assessing impact of deviations and overall quality of the study conduct.
Main Responsibilities
Education
Experience and Skills Required
Location: Montreal , Quebec
Caprion – HistoGeneX est une société en pleine croissance et un laboratoire de recherche clinique de premier plan qui fournit des plateformes intégrées de pointe pour effectuer la surveillance immunitaire, la génomique, l’histopathologie et la protéomique à l’industrie pharmaceutique et biotechnologique. Nos laboratoires spécialisés favorisent le développement et l’évolution de la médecine de précision en prenant en charge l’ensemble du cycle de développement des médicaments, depuis les essais précliniques jusqu’aux essais cliniques de phase finale en passant par les diagnostics complémentaires, conformément aux accréditations de qualité et réglementaires rigoureuses.
Nos laboratoires situés au Canada (Montréal, Québec), en Europe (Anvers & Gosselies, Belgique), aux États-Unis (Californie & Chicago), en Australie et en Chine (Jining) nous permettent d’offrir nos services à l’échelle mondiale.
Le poste de directeur des ressources humaines (Canada) de Caprion - HistoGeneX est une occasion passionnante pour un responsable des RH chevronné d’aider une entreprise à passer au niveau supérieur. Vous serez, notamment responsable de l’élaboration et de la mise en œuvre des initiatives en matière de ressources humaines, en accord avec les objectifs stratégiques de l’entreprise.
Ce poste est orienté sur la pratique visant à équilibrer Les volets stratégiques et tactiques tout en gérant l’ensemble des programmes de RH, y compris l’acquisition et la gestion des talents, la rémunération et les avantages sociaux, le développement et l’engagement des employés, les politiques et la conformité.
Vous aurez à mettre à profit votre expérience, votre passion et votre connaissance des ressources humaines pour améliorer les processus et les politiques en matière de ressources humaines et vous servirez de partenaire à l’équipe de direction de Montréal en faisant preuve de créativité, d’empathie et d’intégrité.
Vous relèverez du vice-président mondial, ressources humaines, basé à Montréal.
Vos responsabilités principales seront les suivantes :
Exigences du profil:
Nous offrons un poste passionnant et stimulant dans un environnement multinational, axé sur le client et où l’innovation est valeur commerciale essentielle.
Location: Montreal , Quebec
Caprion - HistoGeneX is a fast growing company and is a leading clinical research laboratory providing state-of-the-art integrated platforms to perform immune monitoring, genomic, histopathology and proteomics to the pharmaceutical and biotechnology industry. Our specialized laboratories accelerate precision medicine supporting the entire drug development cycle, from preclinical through late stage clinical trials and companion diagnostics under stringent quality and regulatory accreditations.
We offer our services on a global scale through our laboratories in Canada (Montreal, Quebec), Europe (Antwerp & Gosselies, Belgium), the USA (California & Chicago), Australia and China (Jining).
The Director, Human Resources (Canada) at Caprion – HistoGeneX is an exciting opportunity for an experienced HR manager to help take a company to the next level. You will be responsible for developing and implementing the HR initiatives in alignment with the strategic objectives of the organization
This role is expected to be hands-on and balance the strategic with the tactical while managing the full range of HR programs, including talent acquisition and management, compensation and benefits, employee development, employee engagement, policies and compliance.
You will use your experience, passion for, and knowledge of human resources to further improve HR processes and policies and will serve as a partner to the Montreal Management Team with creativity, empathy and integrity
You report to the Global VP, Human Resources, based in Montreal.
Your key responsibilities are:
Profile requirements
We offer an exciting and challenging position in a multinational environment where customer focus and innovation are key business values.
Location: Fremont , CA
Caprion Biosciences Inc. is a leading clinical research organization (CRO) laboratory in immune monitoring, protein characterization and tissue pathology solutions for immunotherapy and drug development. We are located in Montreal, California, Chicago, Belgium, UK, Australia and in China. Employees at Caprion are true scientific partners working together to enhance people’s health and quality of life.
Summary
The Principal Scientist is responsible for the overall conduct of studies in different immune-therapeutic area, overseeing experimental testing design, as well as formulating conclusions and recommendations for next steps. The incumbent has the ability to present Caprion capabilities to clients in a compelling way demonstrating value and differentiation as support function to Business Development activities as well as presentation of results to Sponsor and scientific meetings. The incumbent is ensuring that the timelines and milestones of a study are met by proactively assessing foreseeing challenges, assessing impact of deviations and overall quality of the study conduct.
Main Responsibilities
Education
Experience and Skills Required
Location: Gosselies
Position Summary
Leads method validation, assay transfer and sample analysis studies based on approved driving documents. Prepares and/or reviews experimental documentation for assigned studies. Prepares and/or fills associated documentation relevant to the studies as per appropriate SOP/CSP and applicable regulatory requirements. Writes and reviews method procedures (SOP/CSP). Responsible for binder submission to QA and answering of QA audit reports.
Responsabilities:
The applicant must :
Profile:
Location: Gosselies
Position Summary
Responsible for planning, organizing and overseeing the collection and shipping of biosamples to and from Caprion Biosciences S.A, to ensure timely delivery.
Responsibilities:
The applicant must :
Profile:
Location: Gosselies
Position Summary:
Performs quality control activities relevant to her field of expertise. Reviews study experimental documentation and data based on appropriate driving documents, SOP/CSP following GLP regulations and GCLP guidelines. Review procedures (SOP/CSP).
Responsabilities:
The applicant must :
Profile:
Location: Naperville , IL
Caprion HistoGeneX is currently recruiting a motivated HR Manager. You will be responsible for developing and implementing the HR initiatives in alignment with the strategic objectives of the organization.
You will be responsible for all aspects of HR (recruitment and talent management, people engagement payroll & benefits, remuneration packages and training and development,) and you provide HR support to our business leaders across two US sites (Fremont, California & Naperville, Illinois).
You report to the global VP, Human Resources, based in Montreal.
Your key responsibilities are:
Profile requirements
We offer an exciting and challenging position in a multinational environment where customer focus and innovation are key business values.
Location: Montréal , Québec
Établi au centre-ville de Montréal, avec des sites en Europe et aux États-Unis, Caprion est un chef de file en recherche sous contrat connaissant une forte croissance. Depuis notre fondation en 2000, nous fournissons des services spécialisés d’analyse bioanalytique et de découverte de biomarqueurs, mettant à profit notre expertise de pointe dans les domaines de la protéomique, de la surveillance immunitaire clinique, de l’immunologie et de la bio-informatique. En faisant équipe avec nos scientifiques, nos clients accèdent à une équipe scientifique unique et de calibre international.
Sommaire
Le scientifique principal chez Caprion Biosciences, au sein de l’unité d’affaire ImmuneCarta, est le lead scientifique pour les études en immune monitoring en support aux essais cliniques et aux études pré-cliniques. Le scientifique principal participe au design, au développement et à la validation des essais in vitro. De plus, il est le premier point de contact avec les Sponsors, leurs fournissant un sommaire des données, des présentations et des rapports. Il participe aussi au troubleshooting. Finalement, le scientifique principal est en charge des aspects scientifiques et réglementaires des études en immune monitoring.
Principales Responsabilités
Formation Requise
Expérience et Connaissances Exigées
Conditions de travail
Location: Gosselies
Function :
Reporting to the Associate Director, 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 (phenotyping, receptor occupancy, phosflow, ICS, etc) ELISPOT, ELISA, and viral neutralization tests.
Responsibilities include:
Profile of the applicant:
The applicant must hold a doctorate degree in life science, with strong knowledge of immunology, and preferably with post-doctoral experience (or equivalent). Experience in the industry is a strong asset.
The applicant must :
Offer :
Location: Gosselies
Function :
Reporting to the Laboratory Team Leader and working closely with Principal Scientists, the Research Assistant 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 flow cytometry assays, viral neutralization assays, foci forming unit assays, Luminex and ELISA assays.
Tasks include :
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. One or two years of demonstrated experience in techniques related to cellular and humoral immunology is preferred.
The applicant must :
Offer :
Interested?
Please, send your CV along with a short introduction letter. Additional information may be obtained by calling 071/96.23.36.
Your application and any information will be treated confidentially.
Location: Gosselies
Fonction :
Se rapportant au Chef d’Equipe du Laboratoire et travaillant en étroite collaboration avec les Scientifiques Principaux, l’Assistant(e) de Recherche travaillera avec une équipe se concentrant sur la caractérisation de la réponse immunitaire cellulaire et humorale. Les principales responsabilités incluront le développement et l’exécution de tests de cytométrie en flux, de neutralisation virale, des tests du type « Luminex » et des ELISA.
Les tâches incluent :
Profil du/de la candidat(e):
Le/la candidat(e) doit posséder un bachelier (ou équivalent) en sciences de la vie tel que biologie, biologie médicale ou biochimie/biotechnologie. Une expérience d’un an ou deux en techniques relatives à l’immunologie cellulaire et humorale est souhaitée.
Le/la candidat(e) doit :
Offre :
Intéressé(e) ?
Faites parvenir votre CV ainsi qu’une courte lettre de motivation adaptée. Tout renseignement complémentaire peut également être obtenu au 071/96.23.36.
Votre candidature et informations associées seront traitées de manière confidentielle.