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.
GO FURTHER
MOVE WITH CONFIDENCE
MAKE A DIFFERENCE
Click here for job opportunities at our Lake Forest site in California!
Location: Gosselies , Wallonie
Research Associate – ATU
Summary
The incumbent will be involved in the optimization and qualification of flow cytometry and ELISpot assays. He/She will prepare and review procedures and experimental documentation for methods. Finally, the incumbent will lead all aspects of a given development study.
Who we are
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.
What we offer
Main Responsibilities
Education
Main Requirements
Location: Gosselies , Wallonie
Talent Acquisition Specialist (Hybrid or Remote)
Join a dynamic and fast-growing biotech company as a Senior Talent Acquisition Specialist! As part of the HR team, you will have the exciting opportunity to build and shape the company's future by attracting top scientists and researchers in the field of immunology. With your expertise and drive, you will play a crucial role in helping the company reach new heights and drive innovation in the biotech industry.
Summary
To support the growth, we are seeking a Senior Talent Acquisition Specialist for our team in Gosselies, Belgium. In this role, you will work closely with the other members of Human Resources with the prime function being talent acquisition. The Senior Talent Acquisition Specialist plays a leadership role in the attraction and hiring of new talent while being an ambassador of our values. This role is an opportunity for a dynamic individual who is people-oriented, possesses excellent influencing skills and customer service, combined with the ability to adapt to change and changing priorities.
Main Responsibilities
Must have
Benefits
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
We offer a wide range of benefits including:
About Us
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Montreal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Relevant à la Directrice de gestion de programmes, le Gestionnaire de programme organise et coordonne 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.
Responsabilités principales
Éducation
Compétences et experience requis
Conditions de travail
______________________
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
Reporting to the Director, Program Management, the Program Manager organizes and coordinate scientific programs. The Program Manager provides strategic guidance to teams and Principal Scientists to align with the company’s objectives, as well as Sponsors’ needs.
Responsibilities
Education
Main Requirements
Working Conditions
Location: Gosselies , Wallonie
Junior IT Operations Specialist
Looking for an exciting opportunity to kick-start your IT operations career in a fast-paced, dynamic environment? Do you have a strong background in IT operations and a desire to make a real impact in the world? If so, we have the perfect opportunity for you! Join our team at CellCarta, a global biotech company at the forefront of cutting-edge research and innovation. As a Junior IT Operations Specialist, you will play a critical role in supporting the smooth functioning of our technology systems and ensuring the seamless delivery of vital services to our customers.
We are currently recruiting a Junior IT Operations Specialist.
Department: IT
Location: Gosselies (Charleroi) and Wilrijk (Antwerp) – Global role from Belgium
Summary
The Junior IT Operations Specialist works as member of the global CellCarta IT team, providing first-line IT support and ensuring that all IT infrastructure activities are performed according to CellCarta procedures. Besides the IT support, this job function also expects to liaison with the Global CSV team for Computer System Validation activities to ensure applications and devices are tested, qualified and / or validated for their intended use, in accordance to the company’s global CSV process.
The Junior IT Operations Specialist reports to the Team Manager End-User, Cloud and Platform Services Europe-Asia.
Main responsibilities
The Junior IT Operations Specialist contributes in following IT tasks:
Main Requirements
What can we offer
About Us
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Montréal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 1,000 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé
Le/la spécialiste de l'amélioration de la qualité devra (i) gérer la documentation des exceptions (par exemple, les enquêtes, les déviations, les CAPA), (ii) compiler les données et effectuer des analyses de tendances et d'autres analytiques, (iii) créer des tableaux de bord pour suivre les performances, (iv) proposer des améliorations pour renforcer la robustesse des processus et des systèmes, minimiser les erreurs répétées et favoriser l'amélioration continue des opérations.
Responsabilités
Formation
Exigences principales
Location: Gosselies
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 1,000 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé
Le/la spécialiste de l'amélioration de la qualité devra (i) gérer la documentation des exceptions (par exemple, les enquêtes, les déviations, les CAPA), (ii) compiler les données et effectuer des analyses de tendances et d'autres analytiques, (iii) créer des tableaux de bord pour suivre les performances, (iv) proposer des améliorations pour renforcer la robustesse des processus et des systèmes, minimiser les erreurs répétées et favoriser l'amélioration continue des opérations.
Responsabilités
Formation
Exigences principales
Location: Montreal , QC
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 1,000 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The Quality Improvement Specialist will (i) manage exception documentation (e.g., investigations, deviations, CAPAs) (ii) compile data and perform trend analyses and other analytics, (iii) build dashboards to track performance, (iv) propose improvements to enhance robustness of processes and systems, minimizing repeat errors and drive continuous improvement in the operation.
Responsibilities
Education
Main Requirements
Location: Montreal , QC
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The Group Leader is responsible for the day-to-day management of DAU clinical analysts. In this role, the incumbent is responsible for planning analysis work for all ongoing studies. He/she ensures that the staff is properly trained and competent with all the analytical processes used and monitors the performance of the staff. He/she also monitors the quality of the analysis and documentation to ensure compliance with applicable requirements.
Responsibilities
Education
Main Requirements
Location: Naperville , IL
CellCarta, a leading integrated pathology laboratory and global contract research organization, is seeking a full-time Laboratory Technologist at their Naperville Illinois location to support their offerings in single and multiplexed immunofluorescence & immunohistochemistry and molecular pathology services to pharmaceutical companies and biotechs worldwide. If you want to develop your career path, with the potential to move into other related areas to enhance your skill sets, then our rapidly growing organization might be the next step you need to take!
Job responsibilities
Qualifications
Benefits
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
We offer a wide range of benefits including:
About Us
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Supplemental Information
Candidates must be legally authorized to work in the United States on a permanent basis. Verification of employment eligibility will be required at the time of hire. Visa sponsorship is not available.
Location: Naperville , IL
Position Summary
CellCarta is seeking an entry-level Bio Sample Shipping Clerk to work closely with the Laboratory Section Head of Bio Sample Management for the logistics and tracking of clinical trial shipments.
Main Responsibilities
Education & Required Qualifications
Location: Montréal , QC
Résumé
En tant qu'organisme de recherche mondial pour l'industrie biopharmaceutique, CellCarta (anciennement Caprion - HistoGeneX) donne accès à une large sélection de plateformes et de services de biomarqueurs. Nous nous associons à nos clients pour répondre aux besoins les plus complexes en matière de tests scientifiques, en proposant des solutions personnalisées de tests de biomarqueurs afin de faire progresser le potentiel illimité de la médecine de précision.
Nous proposons nos services à l'échelle mondiale grâce à nos laboratoires aux États-Unis, au Canada, en Belgique, en Chine et en Australie. En combinant notre expertise en histopathologie, en surveillance immunitaire, en protéomique, en génomique et en logistique des échantillons, nous soutenons les entreprises pharmaceutiques et biotechnologiques dans la recherche et le développement de nouveaux médicaments innovants pour le traitement du cancer et des maladies immunitaires. Travaillant dans le cadre d'exigences strictes en matière de qualité et de réglementation, nous nous efforçons de faire la différence dans les futures solutions de traitement proposées aux patients.
CellCarta s'appuie sur sa forte expertise dans le domaine du cancer pour soutenir l'ensemble des services liés aux biomarqueurs, notamment la découverte de biomarqueurs dans la phase de recherche, le profilage des tumeurs et le suivi des biomarqueurs dans les études cliniques et les études d'enregistrement des diagnostics compagnons, le diagnostic des patients et le développement de nouvelles techniques et de nouveaux tests pour l'analyse des tumeurs et la prédiction de la réponse au traitement. L'entreprise comble le fossé entre la recherche, les études cliniques et les diagnostics.
Dans le cadre de l'équipe LIMS Ecosystem, CellCarta est à la recherche d'un(e) analyste technique, basé dans la région de Montréal (Canada). Au sein de l'équipe, vous vous concentrerez sur le LIMS (StarLims) et les applications connexes. Ce rôle est essentiel pour permettre à l'entreprise d'évoluer et d'offrir une certaine flexibilité, car le LIMS est l'un des principaux piliers de l'entreprise.
Ce rôle suppose une connaissance approfondie de l'entreprise, une coordination des différentes activités commerciales, un solide contexte technique, une communication étendue avec les responsables commerciaux, ainsi qu'avec les responsables informatiques internes et externes, dans un environnement modial. Si vous souhaitez contribuer à façonner l'avenir d'une entreprise en pleine croissance, en combinant des compétences techniques en informatique avec un environnement de laboratoire intéressant, ce poste est fait pour vous ! L'agilité et la valeur ajoutée effective pour l'équipe et l'entreprise sont des critères essentiels.
Le ou la candidat(e) idéal(e) a une formation en (bio-) informatique et montre un grand intérêt pour l'apprentissage et le développement de son exposition au laboratoire ; il ou elle fait preuve d'un esprit analytique et d'excellentes aptitudes à la communication, a la capacité d'avoir une vue globale et peut démontrer son expérience à un niveau opérationnel et tactile.
Responsabilités
Le ou la candidat(e) idéal(e)
Ce que nous offrons
Lieu de base
Location:
QUALITY COMPUTER SYSTEM VALIDATION SPECIALIST
Join a dynamic and innovative biotech company as a System Validation Specialist! As an experienced professional, you will have the opportunity to leverage your expertise in software quality assurance and computer system validation. Your contributions will play a key role in ensuring the quality and reliability of mission-critical systems, and you will have the satisfaction of knowing that your work is making a difference in the lives of people.
Summary
The Quality Computer System Validation Specialist supports the Software Quality Assurance/validation of computer systems, software applications, and lab equipment used at CellCarta. This position can be based anywhere in Belgium or France.
This position participates in Software Quality Assurance, system validation projects company wide, provides instruction and guidance on validation, supports lab equipment qualification, facilitate system change management and interfaces with subject matter experts, users, project managers, Compliance, and QA. The position is also involved in the development of a software quality framework.
Main Responsibilities
Education
Main Requirements
Additional Requirements
Benefits
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
We offer a wide range of benefits including:
About Us
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Montreal , QC
Background
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.
As part of the LIMS Ecosystem team, CellCarta is looking for a Technical Analyst, based in the Montreal area (Canada). As part of the team, you will be focusing on the LIMS (StarLims) and related applications. This role is critical to allow the company to scale and provide flexibility as LIMS is one of the major backbones of the company.
This role assumes a profound business acumen coordinating the different business activities with a strong technical background, extensive communication with business, as well as IT internal and external stakeholders, in a global environment. If you want to shape the future of a rapidly growing company, combining technical IT skills with an interesting lab environment, this role is a match for you! Agility and effective added value to the team and the company are key criteria.
The ideal candidate has an (Bio-) IT background, and shows a genuine interest in learning and developing their lab exposure; s/he demonstrates an analytical mind and great communication skills, has the ability to see the big picture, and can prove experience at an operational and tactical level.
Responsibilities
The Ideal Candidate
What We Offer
Base Location
Location: Wilrijk , Antwerp
Team Manager IT Infra & Service Management Europe-Asia
CellCarta is looking for a Team Manager IT Infra & Service Management Europe-Asia.
Heading your team as a technical and people manager, you will report to the Senior Director IT Europe & Asia. You will make sure that your team is focusing on a variety of Infrastructure and (ITIL) service management areas in our locations Europe and Asia. Your main location is our European HQ in Antwerp (Wilrijk). You need to be well versed in Infrastructure environments including deployment and service management automation related to these services. Service Management supporting the people on site and remotely is a crucial part of your time. Experience in areas like server, storage and hybrid cloud environments is an add-on. Apart from your IT technical and people focus, you will liaise with the local businesses in day to day support but also tactical improvements.
The business as well as the IT technical area are in great transition. We grow both organically and non-organically via acquisitions. If you want to shape the future of a rapidly growing leader in Precision Medicine, combining technical IT skills with an interesting lab environment, then this role is a match for you. As we are still a mid-size company you will have the ability to get additional skills with overarch end-user. With the implementation of an acquisition amalgamation strategy, you will not only have the ability to work with the newest tools and environments, you will also be able to advise. Agility and added value to the team and the company are key criteria. The ideal candidate has an analytical mind and good communication skills, experience at the operational technical level, and a proven experience in managing and engaging teams. Experience in managing teams remotely is a must.
Major responsibilities:
The ideal candidate:
What can we offer:
About Us:
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Dartmouth , NS
Clinical Logistics, a CellCarta company was founded in 2002. Clinical Logistics has supported clinical trials in over 50 countries. The company has earned a reputation for quality and customer service excellence with some of the largest pharmaceutical companies, biotechs and CROs. Answering an unmet need in the marketplace for high quality handling of critical samples from clinical trial sites to the laboratory, CLI is positioned as a key player in clinical trial logistics with a focus on specialty specimens. Clinical Logistics services also include assembly and distribution of kits for pharmacokinetic / pharmacodynamic (PK/PD) and pharmacogenomic (PG) sample collection and shipping.
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
As a member of CellCarta's logistics SSTP team, this role reports to the Director of Quality Assurance, Logistic Division; the incumbent in this role supervises a team of employees in a sample shipment tracking and processing department. The main objective of the role is to monitor daily performance, handle issues, and ensure the team meets its goals and deadlines.
Responsibilities
Qualifications
Working Conditions
Benefits
Location: Gosselies , Wallonie
Technicien(ne) chargé(e) de la paie (à temps partiel)
CellCarta est un laboratoire de recherche clinique (CRO) leader dans le domaine de la surveillance immunitaire, de la caractérisation des protéines et des solutions de pathologie tissulaire pour l'immunothérapie et le développement de médicaments. Nous sommes situés à Montréal, en Californie, à Chicago, en Belgique, en Australie et en Chine. Les employés de CellCarta sont de véritables partenaires scientifiques qui travaillent ensemble pour améliorer la santé et la qualité de vie des gens.
Nous recherchons un(e) technicien(ne) de la paie qui serez responsable de l'administration des salaires et du programme d'avantages extra-légaux de l'entreprise Wallonie et France. Vous serez le principal point de contact pour les employés et les secrétariat sociaux en ce qui concerne les questions relatives aux avantages sociaux et à la paie et pour la résolution de problèmes.
Principales responsabilités
Qualifications et exigences
Location: Charleroi , Charleroi
ABOUT US
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
MISSION
KEY RESPONSIBILITIES
QUALIFICATIONS REQUIRED
Location: Wilrijk , Antwerp
Functie
Wij hebben voor jou een unieke mogelijkheid om aan de slag te gaan in onze afdeling “Biosample Management”. Binnen deze afdeling van zo’n 35 collega’s worden binnenkomende stalen geregistreerd in het Labo informatie management systeem (StarLIMS), 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. Je begrijpt dat dit werk cruciaal is om achteraf correcte en zo goed mogelijke analyseresultaten te kunnen produceren.
Als “Logistiek Teamleader (Head Biosample Operator)” ondersteun je het afdelingshoofd Biosample management, vooral qua interne en externe staal- en reagentialogistiek, bij het identificeren van procesverbeteringen samen met de biosample operators. Deze gaan van het oplossen en vermijden van terugkerende issues, over het zorgen dat CellCarta compliant is en blijft met de internationale shipping and customs regulation, tot algemene administratieve procesvereenvoudigingen en optimalisaties. Je zal mee helpen bij de motivatie van deze procesverbeteringen, ook naar budgetten en resources toe. Tot slot zal je mee helpen bij het introduceren en opvolgen van deze procesverbeteringen binnen het team van biosample operators, zodat deze globaal gealigneerd zijn en blijven. Jij houdt hen scherp, weet hen te motiveren en versterkt hun verantwoordelijkheidszin en dit team kan op je rekenen qua technische ondersteuning.
Profiel
Location: Montreal , QC
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 1000 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The Lab Data Reviewer (LIMS) is responsible to a) migrate data from previously used inventory systems to StarLIMS while maintaining all appropriate documentation; b) communicate with the laboratory and other teams to complete data migration from previously used inventory systems to StarLIMS; c) review the sample reception data entry in StarLIMS; d) dispose and organize samples in storage units, in link with data migration.
Responsibilities
Education
Main Requirements
Working Conditions
Location: Montréal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 1000 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le réviseur de données de laboratoire (LIMS) est chargé(e) de : a) migrer les données des systèmes d'inventaire précédemment utilisés vers StarLIMS tout en conservant toute la documentation appropriée ; b) communiquer avec le laboratoire et les autres équipes pour achever la migration des données des systèmes d'inventaire précédemment utilisés vers StarLIMS ; c) revoir la saisie des données de réception des échantillons dans StarLIMS ; d) disposer et organiser les échantillons dans les unités de stockage, en lien avec la migration des données.
Responsabilités principales
Éducation
Compétences et expérience requis
Conditions de travail
Location: Montreal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le chef de groupe est responsable de la gestion quotidienne des analystes cliniques de l'UAD. À ce titre, il est responsable de la planification du travail d'analyse pour toutes les études en cours. Il/elle s'assure que le personnel est correctement formé et compétent pour tous les processus analytiques utilisés et contrôle les performances du personnel. Il/elle contrôle également la qualité de l'analyse et de la documentation afin de garantir la conformité aux exigences applicables.
Responsabilités principales
Éducation
Compétences et experience requis
Location: Montreal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le chercheur scientifique I est chargé d'assurer la qualité de l'analyse, de l'examen et de l'interprétation des données ; il effectue l'analyse des données afin de garantir l'intégrité scientifique, la conformité aux SOP/CSP et aux exigences réglementaires applicables. Le chercheur scientifique I travaille en étroite collaboration avec les superviseurs de l'unité d'analyse des données, l'équipe scientifique et le spécialiste de la cytométrie en flux pour résoudre les problèmes techniques/scientifiques et les problèmes généraux du projet ; il interagit avec l'assurance qualité pour résoudre les problèmes de qualité.
Responsabilités principales
Éducation
Compétences et experience requis
________________________________
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The Research Scientist I is responsible for ensuring high-quality analysis, review and interpretation of data; They perform the analysis of data to ensure scientific integrity, compliance with SOP/CSP and applicable regulatory requirements. The Research Scientist I works closely with the supervisors of the Data Analysis Unit, the Scientific Team, and the Flow Cytometry Specialist to address technical/scientific and general project issues; They interact with Quality Assurance to address quality issues.
Responsibilities
Education
Main Requirements
Location: Dartmouth , NS
Clinical Logistics, a CellCarta company was founded in 2002. Clinical Logistics has supported clinical trials in over 50 countries. The company has earned a reputation for quality and customer service excellence with some of the largest pharmaceutical companies, biotechs and CROs. Answering an unmet need in the marketplace for high quality handling of critical samples from clinical trial sites to the laboratory, CLI is positioned as a key player in clinical trial logistics with a focus on specialty specimens. Clinical Logistics services also include assembly and distribution of kits for pharmacokinetic / pharmacodynamic (PK/PD) and pharmacogenomic (PG) sample collection and shipping.
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
As a member of CellCarta's logistics Operations team, this role reports to the General Manager, Logistic Division the incumbent in this role improves operational management systems and is responsible for production KPI’s. The Production Manager is responsible for overseeing the operations process in a manufacturing environment, ensuring that goods are produced efficiently, on time, within budget, and to the required quality standards.
Key Responsibilities
Qualifications
Physical Demands
Working Conditions
Other
Although the duties outlined constitute the bulk of what a Production Manager is responsible for, due to the nature of our business all Logistics employees are cross trained in operations and quality control to ensure timely, high-quality products and service for our customers.
Benefits
Location: Naperville , IL
Join a dynamic and innovative biotech company as a System Validation Specialist! As an experienced professional, you will have the opportunity to leverage your expertise in software quality assurance and computer system validation. Your contributions will play a key role in ensuring the quality and reliability of mission-critical systems, and you will have the satisfaction of knowing that your work is making a difference in the lives of people.
Summary
The Quality Computer System Validation Specialist supports the Software Quality Assurance/validation of computer systems, software applications, and lab equipment used at CellCarta. This position can be based anywhere in the US.
This position participates in Software Quality Assurance, system validation projects company wide, provides instruction and guidance on validation, supports lab equipment qualification, facilitate system change management and interfaces with subject matter experts, users, project managers, Compliance, and QA. The position is also involved in the development of a software quality framework.
Main Responsibilities
Education
Main Requirements
Additional Requirements
Benefits
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
We offer a wide range of benefits including:
About Us
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Montreal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 1,000 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
Relevant du directeur de l'assurance qualité, l'associé(e) assurance qualité (AQ) est chargé(e) de mener des audits et des révisions de l'assurance qualité et de présenter des rapports à ce sujet. L'associé AQ soutient le département AQ dans l'évaluation de la conformité des études cliniques et non cliniques avec les réglementations, les directives, les protocoles d'étude, les plans d'étude et les procédures opérationnelles standard (SOP) de l'entreprise.
Principales responsabilités
Formation
Exigences principales
Conditions de travail
_________________________________________
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 1,000 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
Reporting to the Director of Quality Assurance, the Quality Assurance (QA) Associate is responsible for conducting and reporting quality assurance audits and reviews as scheduled. The QA Associate supports the QA department in assessing compliance of clinical and non-clinical studies with applicable regulations, guidelines, study protocols, study plans and company SOPs.
Responsibilities
Education
Main Requirements
Working Conditions
Location: Naperville , IL
Laboratory Manager
Seize a unique opportunity to lead the lab operations of a cutting-edge biotech company and make a difference in the healthcare industry! In this critical role, you will be the driving force behind seamless day-to-day lab operations and play a key role in advancing cutting-edge biotech solutions. If you're a leader with a passion for science and a track record of success, this is your opportunity to thrive in a fast-paced, dynamic environment.
Summary
The laboratory manager is responsible for the day-to-day management of laboratory sections (BSM, PAX, IHC/ISH/IF, DNA/RNA). He/she ensures that the staff is properly trained and competent with all the techniques used and monitors the performance of the staff. He/she also monitors the quality of the laboratory's work and documentation to ensure compliance with applicable requirements. He/she takes responsibility for all aspects of the lab, including equipment, employees, supplies, software, and documentation.
Responsibilities
Quality & regulatory responsibilities
People management & planning
Lab/Technical responsibilities
Admin tasks & communication
Qualification and Skills
Benefits
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
We offer a wide range of benefits including:
About Us
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Naperville , IL
Clinical Data Manager
As a global Research Organization to the biopharmaceutical industry, CellCarta 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'd love to find a Clinical Data Manager to help us serve our sophisticated customers while adhering to our rigorous but sensible procedures.
Summary
As a Clinical Data Manager based in our Naperville, IL office, you will learn to ensure clinical study data are collected, handled and validated in an appropriate and consistent manner to ensure a high quality database is delivered for statistical analysis within the agreed upon project timelines. You will need to be comfortable doing the following:
If you are organized, analytically minded, possess a solid technical background, have a passion for IT and thrive in a dynamic, high complexity environment, this might just be the role you are looking for.
Required education
Bachelor’s degree in Life Sciences, Computer Science, Mathematics, Statistics, Pharmaceuticals Sciences, or related fields or 1+ years of industry related experience.
Responsibilities
The main responsibilities of a Clinical Data Manager are:
Qualification and Skills
It's great, but not required, if you have:
This position is full-time, 40 hours, Monday through Friday. EOE M/F/D/V
Supplemental Information
Candidates must be legally authorized to work in the United States on a permanent basis. Verification of employment eligibility will be required at the time of hire. Visa sponsorship is not available.
Benefits:
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
We offer a wide range of benefits including:
About Us
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Naperville , IL
Clinical Project Manager (CPM) – Naperville, IL, USA
Are you ready to launch your career in the exciting world of clinical trials and biotech? We're seeking a driven and detail-oriented Clinical Project Manager to join our dynamic team. This entry-level role offers the opportunity to gain hands-on experience and grow your expertise in a fast-paced, innovative environment. As a key member of our team, you will have the opportunity to work with cutting-edge technology, collaborate with cross-functional teams, and gain valuable experience in project management. Get ready to take your first step in a rewarding career in the biotech industry and join us today!
Summary
We're looking for a Clinical Project Manager to help us serve our sophisticated customers while adhering to our rigorous but sensible procedures.
As a CellCarta Clinical Project Manager (CPM) you learn the entire business model and you will usually be the first to discover what our customers need. As a CellCarta CPM, you’re ultimately responsible for embodying 3T’s. Always keep the project on Task, on Track and on Time.
You will need to be comfortable doing the following:
If you are organized, analytically minded, possess a solid technical background and will thrive in our dynamic, high complexity environment, this might just be the role you are looking for.
Purpose of the function
To drive and manage projects with internal stakeholders and external customers (pharma and biotech partners in oncology) in order to deliver results on time in full and in agreement with the CellCarta Quality System. CPMs have project management skills and are able to hold scientific discussions with the sponsor in relation to the project. CPMs are part of the Clinical Operation group.
Responsibilities
The CPM is responsible for the delivery of clinical projects within the agreed scope, time and budget, primarily by coordinating a multitude of tasks performed by internal and external partners. The CPM ensures that the project is accomplished within the quality system of CellCarta. His/Her responsibility starts when a clinical project is granted to CellCarta and finishes when the project is delivered to the sponsor, study properly archived and final invoicing prepared.
Additional responsibilities
Required education
A Masters degree in Biology or Biochemistry, Biomedical Sciences, Pharmaceutical Sciences, Medicine or a Bachelors degree with experience.
Qualification and Skills
The Clinical Project Manager uses an arsenal of skills to successfully perform the required tasks.
On your first day, it will be beneficial for you to have:
It's great, but not required, if you have
Benefits
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
We offer a wide range of benefits including:
About Us
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Gosselies
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire du poste
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 sont l’exécution de tests de cytométrie en flux, de neutralisation virale, des tests ELISA.
Ce poste requiert de travailler sur les quarts de soir et de weekend en rotation sur l'horaire qui suit:
Lundi - Vendredi (13h30-22h00)
Mercredi - Dimanche (9h00-17h30)
Principales responsabilités
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.
Offre
Votre candidature et informations associées seront traitées de manière confidentielle.
Location: Gosselies , Wallonie
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
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 sont l’exécution de tests de cytométrie en flux, de neutralisation virale, des tests ELISA.
Ce poste requiert de travailler sur les quarts de soir et de weekend en rotation sur l'horaire qui suit:
Lundi - Vendredi (13h30-22h00)
Mercredi - Dimanche (9h00-17h30)
Principales responsabilités
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.
Offre
Votre candidature et informations associées seront traitées de manière confidentielle.
Location: Gosselies , Wallonie
Principal Scientist (Hybrid)
Take the lead in shaping the future of immunology at a fast-growing biotech company! As a Principal Scientist, you will have the chance to drive innovation and breakthroughs in the field by leveraging your expertise and passion. With your knowledge and dedication, you will play a critical role in the company's growth and success, helping to advance the cutting-edge research and development in the dynamic world of biotech.
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.
This is a 50% remote position
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:
Benefits:
CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world!
We offer a wide range of benefits including:
About Us:
CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices.
Join us as we make an impact on the future of patient therapy!
Location: Gosselies , Wallonie
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 1000 employees in its 11 facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
The project Lead will lead 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.
Responsibilities:
The applicant must:
Profile:
Location: Montreal , QC
À propos de CellCarta
CellCarta est un important fournisseur de services de laboratoire spécialisés en médecine de précision pour l'industrie biopharmaceutique. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La société opère à l'échelle mondiale avec 11 installations situées au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
CellCarta est à la recherche d’un(e) Gestionnaire des opérations, échantillons biologiques, pour être responsable de gérer et de superviser efficacement les équipes suivantes : Éthique et approvisionnement en échantillons, Manutention - Matériel de laboratoire, et Manutention – Échantillons de laboratoire, afin qu'ils respectent les objectifs et les échéanciers. Cette personne est également responsable de mener différents projets liés à l'amélioration efficace des processus et à la bonne qualité du travail et des services chez CellCarta.
Principales responsabilités
Formation
Exigences principales
________________________________________________________________________________________
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
CellCarta is seeking a Biosample Operations Manager to effectively lead and manage the following teams: Ethics and Sample Procurement, Manutention - Laboratory Material, and Sample Handling services, thus ensuring that they meet the objectives and timelines. This person will also be responsible for leading different projects related to efficient process improvements and the good quality of work and services at CellCarta.
Main Responsibilities
Education
Main Requirements
Location: Montreal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
CellCarta recherche un scientifique très motivé et enthousiaste pour son équipe de protéomique par spectrométrie de masse. Cette personne jouera un rôle clé dans la réalisation d'études impliquant le profilage de peptides par LC-MS, le séquençage de peptides à l'aide de MS en tandem, le développement de méthodes SRM, ainsi que l'analyse et l'interprétation de données SRM de peptides ciblés. En outre, le scientifique peut également être impliqué dans la préparation d'échantillons de fluides biologiques et d'échantillons d'étude de tissus impliquant une variété de techniques telles que l'immunodéplétion, la digestion et l'analyse par chromatographie SCX/HPRP suivant les procédures opérationnelles standard (SOP), les bonnes pratiques de laboratoire (GLP) et les bonnes pratiques de documentation.
Responsabilités principals
Éducation
Compétences et experience requis
Conditions de travail
_____________________________
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
CellCarta is seeking a highly-motivated and enthusiastic Scientist for its Mass Spectrometry Proteomics team. This individual will play a key role in performing studies involving peptide profiling by LC-MS, peptide sequencing using tandem MS, SRM method development, and targeted peptide SRM data analysis and interpretation. In addition, the Scientist may also be involved in sample preparation of biological fluids and tissue study samples involving a variety of techniques such as immuno-depletion, digestion and analysis by SCX/HPRP Chromatography following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) and Good Documentation Practices.
Responsibilities
Education
Main requirements
Working Conditions
Location: , Antwerp
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in histopathology, genomics, immunology, and proteomics as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with 11 facilities located in Canada, the USA, Belgium, Australia, and China.
Job Summary
As part of the Client Services team, you will work closely with Client Managers, Business Development, and relevant stakeholders in Operations. The Proposal Specialist prepares budget proposals and task orders related to our histopathology and genomics services and ensures coordination and tracking through the company’s client relationship management (CRM) system (SalesForce.com).
On-site in our Antwerp, Belgium, facility will be required. Partial remote working will be available following the completion of training.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Job Qualifications
Location: Gosselies , Wallonie
Payroll Technician (part-time)
CellCarta 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, Australia and in China. Employees at CellCarta are true scientific partners working together to enhance people’s health and quality of life.
We are seeking a Payroll Technician (part time) located preferably in Belgium (French side) who will be responsible for administering the company’s payrolls, and benefits program for Belgium and France. You will act as the main point of contact for both employees and external vendors regarding benefits and payroll questions and troubleshoot issues as they arise.
Main Responsibilities
Must have
Location: Montreal , QC
À propos de CellCarta
CellCarta est l’un des principaux fournisseurs de services de laboratoire spécialisés en médecine de précision pour l’industrie biopharmaceutique. Tirant parti de ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi que des services connexes de collecte d’échantillons et de logistique, CellCarta prend en charge l’ensemble du cycle de développement de médicaments, de la découverte aux essais cliniques de stade avancé. La société exerce ses activités à l’échelle mondiale avec plus de 1000 employés dans ses neuf installations situées au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Chez CellCarta, le développement organisationnel consiste à s’assurer que nous amenons nos employés à leur plein potentiel, cultivons un environnement engageant et productif, construisons des équipes passionnées et performantes et apportons des solutions stratégiques pour maximiser notre performance commerciale et soutenir notre croissance.
Une équipe scientifique qui respecte les plus hauts standards de qualité.
Résumé
Votre objectif principal sera d’influencer et de façonner notre stratégie de développement organisationnel afin d’attirer, d’engager et de retenir des collègues talentueux. Vous jouerez un rôle clé dans le soutien d’une expérience positive pour les employés et le développement d’une culture organisationnelle solide alignée sur nos valeurs. En démontrant votre leadership stratégique, votre vision et votre innovation, vous serez responsable de l’évolution continue de notre approche pour identifier, développer et engager les talents dans le monde entier.
Responsabilités
En tant que gardien de l’expérience employé et membre de l’équipe de leadership globale RH, vous allez :
Éducation/Compétences
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, the USA, Belgium, Australia, and China.
At CellCarta, Organizational Development is about ensuring we elevate our people to their highest potential, cultivate an engaging and productive environment, build passionate high-performing teams, and drive strategic solutions to maximize our business performance and support our growth.
A scientific team that upholds the highest quality standards.
Summary
Your primary focus will be to influence and shape our OD strategy to help attract, engage, and retain talented colleagues. You will play a key role in supporting and inspiring a positive employee experience and developing a strong organizational culture aligned with our values. Demonstrating your strategic thought leadership, vision, and innovation, you will be responsible for the continued evolution of our approach to identifying, developing, and engaging talent around the world.
Responsibilities
Education/Skills
Location: Montréal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le/la scientifique principal(e) chez CellCarta, 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/la scientifique principal(e) 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/la scientifique principal(e) est en charge des aspects scientifiques et réglementaires des études en immune monitoring.
Principales Responsabilités
Formation Requise
Expérience et Connaissances Exigées
Conditions de travail
--------
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
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: Naperville , IL
If you have an interest in technically supporting tissue analysis for immune-oncology drug programs and the development of companion diagnostics, and a passion for pathology and personalized medicine, this might be the role you are looking for. We are seeking a full-time Histology Technician(IHC) performing Immunohistochemistry at our Naperville Illinois location to support our offerings in single and multiplexed immunofluorescence & immunohistochemistry and molecular pathology services to pharmaceutical companies and biotechs worldwide.
Responsibilities
and document all quality control activities with the ability to recognize outliers and correct them.
Requirements
About Us
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.
A scientific team that upholds the highest quality standards
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 Laboratories we care about our team and offer a wide range of benefits including:
Join us as we continue to expand internationally and be part of the future of precision medicine.
Location: Montreal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le planificateur de laboratoire relève du coordinateur et est chargé de :
Responsabilités principales
Éducation
Compétences et experience requis
Horaire
________________________________________________________
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The laboratory scheduler reports to the coordinator and is responsible to:
Responsibilities
Education
Main Requirements
Schedule
Location: Montreal , QC
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The LIMS Business Analyst is responsible for: a) supports business processes for the testing and deployment of lab applications; b) collaborates with lab operations to develop and execute user acceptance tests for all deliverables; c) collaborates with IT to design and prepares adequate documentation; d) acts as a subject matter expert; e) gives training and develops user guides and; f) writes, reviews and updates general SOPs as needed.
Responsibilities
Education
Working Conditions
Location: Montréal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire du poste
L'analyste d'affaire des applications LIMS est chargé : a) de soutenir les processus d'affaires pour l'essai et le déploiement des applications de laboratoire ; b) de collaborer avec les opérations de laboratoire pour élaborer et exécuter des tests d'acceptation par les utilisateurs pour tous les produits livrables ; c) de collaborer avec les TI pour concevoir et préparer la documentation adéquate ; d) d'agir en tant qu'expert en la matière ; e) de donner de la formation et d'élaborer des guides de l'utilisateur ; et f) de rédiger, d'examiner et de mettre à jour les procédures opérationnelles normalisées générales, au besoin.
Responsabilités principales
Compétences et expérience requises
Conditions de travail
Location: Gosselies , Wallonie
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 900 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Sous la responsabilité de la chef de groupe, le ou la réviseur de données effectue des activités de contrôle de la qualité de la documentation et des données expérimentales basées sur les documents de conduite appropriés, les SOP / CSP suivant les réglementations BPL et les directives GCLP. Procédures d'examen (SOP / CSP).
Principales Responsabilités
Profil Recherché
Bachelor ou Master en sciences de la vie et un minimum de deux d'expérience en industrie dans un poste similaire
Aptitudes Requises
Ce que nous offrons
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 ISO13485. Reports to Director QA Logistics Division.
Major Responsibilities
• Managing the day to day activities of the QA and QC personnel
• Providing quality service and decisions to the operational functions
• Providing oversight of all QA documentation
• Ensuring timelines for QA activities are met
• Managing suppliers and vendors, including completion and review of vendor questionnaires and audits as required, periodic vendor review
• Managing customer/sponsor audits, audit preparation, host auditor, and manage related CAPAs
• Managing customer requests related to the quality system
• Oversee the quality management system
• Assisting QA/QC with inspecting documents, labels, kits, electronic manifests and other study related materials to ensure that each meets the exact specifications outlined by the sponsor and/or the SOW.
• Ensuring that records are kept of all checking, analyzing, inspecting and reviewing. Ensuring that any non-conformities found are documented and investigated.
• Working with IT department to develop tools to improve the quality system
• As a member of the management team, participate in business development, strategy, and operational effectiveness.
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: Montreal , QC
Reporting to the Director, Program Management, the Manager, Program Management Assistants directly manages the group of Program Management Assistants, and has the following main responsibilities:
Location: Montréal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le/la technicien(ne) LIMS est chargé(e) de : a) migrer les données des systèmes d'inventaire précédemment utilisés vers StarLIMS tout en conservant toute la documentation appropriée ; b) communiquer avec le laboratoire et les autres équipes pour achever la migration des données des systèmes d'inventaire précédemment utilisés vers StarLIMS ; c) revoir la saisie des données de réception des échantillons dans StarLIMS ; d) disposer et organiser les échantillons dans les unités de stockage, en lien avec la migration des données.
Responsabilités principales
Éducation
Compétences et expérience requis
Conditions de travail
Location: Montreal , QC
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The LIMS Technician is responsible to a) migrate data from previously used inventory systems to StarLIMS while maintaining all appropriate documentation; b) communicate with the laboratory and other teams to complete data migration from previously used inventory systems to StarLIMS; c) review the sample reception data entry in StarLIMS; d) dispose and organize samples in storage units, in link with data migration.
Responsibilities
Education
Main Requirements
Working Conditions
Location: Montreal , QC
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The Scientific Writer will assist us to produce study reports and documentation for development, validation and clinical sample analysis projects. As a Scientific Writer, you will be responsible for creating scientific documentation for our projects, including assay development, assay validation and sample analysis reports for different immune monitoring platforms and methodologies. You will also be involved in developing and maintaining templates, reviewing others work to ensure high quality, as well as identifying where processes can be made more efficient, including putting infrastructure tools in place and training other writers to work within new workflows. The successful candidate has an academic or professional background in Immunology and is an experienced writer of scientific, medical, or technical content. You must enjoy working independently, be self-motivated, and love to learn about scientific domains and technologies. You must be able to handle concurrent assignments that have quick turnaround times under strict deadlines with a professional and positive attitude and enjoy mentoring and training others.
Main Responsibilities
Education
Experience and Skills Required
Location: Montréal , QC
À propos de CellCarta
CellCarta est un important fournisseur de services de laboratoire spécialisés en médecine de précision pour l'industrie biopharmaceutique. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La société opère à l'échelle mondiale avec 11 installations situées au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le rédacteur(trice) scientifique nous aidera à produire des rapports d'étude et de la documentation pour des projets de développement, de validation et d'analyse d'échantillons cliniques. En tant que rédacteur scientifique, vous serez responsable de la création de la documentation scientifique pour nos projets, y compris les rapports de développement, de validation et d'analyse d'échantillons pour différentes plateformes et méthodologies de surveillance immunitaire. Vous serez également impliqué(e) dans le développement et la maintenance de modèles, dans la révision du travail des autres afin de garantir une qualité élevée, ainsi que dans l'identification des processus qui peuvent être rendus plus efficaces, y compris la mise en place d'outils d'infrastructure et la formation d'autres rédacteurs pour travailler dans le cadre de nouveaux flux de travail. Le/la candidat(e) retenu(e) a une formation universitaire ou professionnelle en immunologie et est un(e) rédacteur(trice) expérimenté(e) de contenu scientifique, médical ou technique. Vous devez aimer travailler de manière indépendante, être motivé et aimer apprendre des domaines scientifiques et des technologies. Vous devez être capable de gérer des missions simultanées avec des délais d'exécution rapides et des échéances strictes avec une attitude professionnelle et positive et vous aimez encadrer et former les autres.
Principales responsabilités
Formation Requise
Expérience et Connaissances Exigées
Location: Montreal , QC
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
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 , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le scientifique principal chez CellCarta, 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: Montreal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
L’analyste de données en immunologie/virologie occupe différentes fonctions au sein du département d'analyse de données. Ces fonctions incluent l’analyse et la production de rapports concernant les données en cytométrie en flux et de données provenant d’autres plateformes. L'analyste de données doit 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, Unités d’analyse et de gestion de données.
Responsabilités principales
Éducation
Compétences et experience requis
_____________________________________
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The Data Analyst (Immunology/Virology) 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 Director, Data Analysis and Data Management to ensure accurate and timely completion of data analysis. Maintains study-related documentation as per GLP/GCLP and regulatory guidance.
Responsibilities
Education
Main Requirements
Location: Gosselies , Wallonie
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
Reporting to the Group Leader, Sample Management, the Logistics Specialist is mainly responsible for planning, organizing and overseeing the collection and shipping of biosamples to and from CellCarta to ensure timely delivery
Key Responsibilities
Qualifications Required
Location: 9000 , East-Flanders
Biogazelle offers genomic and transcriptomic services, performed in an ISO accredited lab, to support drug development during pre-clinical research and clinical trials. Our customers rely on our expertise in RNA biomarker discovery, assay development and validation; our pioneering role in liquid biopsies and non-coding RNA, and our experience with clinical trials to accelerate the development of their diagnostics and therapeutics. Our service portfolio is built on state-of-the-art technologies such as RNA and DNA sequencing, qPCR and digital PCR, all combined with advanced data analysis methods.
We are an innovative and dynamic company constantly growing and adapting its bioinformatics capabilities. To extend our dry-lab team, we are looking for a motivated senior bioinformatician to work together to transform data into biological knowledge and scientific insights.
Tasks and responsibilities
As Senior Bioinformatician you lead customer projects and internal R&D projects by conceptualizing and performing advanced data analysis tasks:
Competencies and skills
Our offer
We look forward to receiving your motivation letter (clearly mention competences and skills, and relevant experience) and CV to hr@biogazelle.com.
Biogazelle, Technologiepark 82, B-9052 Zwijnaarde, Belgium
Location: Montreal , QC
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Le chef d'équipe de la gestion des données est responsable de l'ensemble des activités de gestion des données dans le cadre des projets assignés, pour une équipe de 5 à 8 gestionnaires de données. Le candidat retenu supervisera les activités de gestion des données, notamment les transferts de données, le suivi des échantillons, la programmation et la gestion des divergences. En outre, le titulaire du poste participera à l'élaboration et à la mise à jour de la documentation relative à la gestion des données, y compris les procédures opérationnelles standard (POS) et le matériel de formation.
Responsabilités principals
Éducation
Compétences et experience requis
Location: Montreal , QC
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
The Data Management Team Lead is responsible for the overall Data Management activities within assigned projects, for a team of 5-8 data managers. The successful candidate will supervise data management activities including data transfers, sample tracking, programming and discrepancy management. Furthermore, the incumbent will assist with development and maintenance of data management documentation including Standard Operating Procedures (SOPs) and training material.
Responsibilities
Education
Main Requirements
Location: Gosselies , Wallonie
À propos de CellCarta
CellCarta est l'un des principaux fournisseurs à l'industrie biopharmaceutique en matière de services de laboratoire spécialisés en médecine de précision. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La compagnie est présente dans le monde entier et emploie plus de 800 personnes dans ses neuf sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire
Location: Wilrijk
Associate Assay Development Scientist Histopathology
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.
Major responsibilities
The assay development unit is responsible for the optimization and validation of high quality (single and multiplex) IHC, RISH, FISH assays for use in clinical trials.
Profile
Job Related competences
Personal competences
We offer an exciting and challenging full-time position in a multinational environment where customer focus and innovation are key business values. You will join a global CRO where your expertise matters and contributions can be felt. You will receive thorough on-the-job-training.
Send your resume and application letter to hgx_people@cellcarta.com
Location: Montreal , QC
À propos de CellCarta
CellCarta est un important fournisseur de services de laboratoire spécialisés en médecine de précision pour l'industrie biopharmaceutique. Grâce à ses plateformes analytiques intégrées en immunologie, histopathologie, protéomique et génomique, ainsi qu'à ses services connexes de collecte d'échantillons et de logistique, CellCarta soutient l'ensemble du cycle de développement des médicaments, de la découverte aux essais cliniques avancés. La société opère à l'échelle mondiale avec 11 installations situées au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Sommaire du poste
CellCarta 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 pour procéder à l'optimisation/développement et à la validation des méthodes. Il ou elle devra également procéder à 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).
Responsabilités principales
Compétences et expérience requises
________________________________________________________
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
CellCarta is seeking a highly motivated and enthusiastic Scientist with strong background and hands-on experience in immunoassays (MSD and ELISA). This individual will play a key role in performing method optimization/development as well as validation. The individual will also be required to analyze samples on a variety of biological fluids and tissue study samples following Standard Operating Procedures (SOP) and Good Laboratory Practices (GLP).
Main Responsibilities
Experience and skills required
Location: Gosselies , Wallonia
About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 800 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Key Responsibilities
Reporting to the Vice President of Scientific Lab Operations, the Site Head is responsible for the operational, and financial success of the site and laboratory. This includes, and is not limited to;
Qualifications
Postgraduate degree (M.Sc or Ph.D) in a Life Science field (Immunology, Cell Biology, Biochemistry etc.). Previous experience in Business Management with P&L responsibility within a CRO environment is preferred.
Location: Wilrijk , Antwerp
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
Wilrijk, Antwerpen (Belgie)
Functie
Wij hebben voor jou een unieke mogelijkheid om als schoolverlater of laborant(e) met ervaring bij ons aan de slag te gaan in de afdeling ‘Biosample Management’ waar binnenkomende stalen geregistreerd worden in het Labo informatie management systeem, verplaatst worden 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
• Bachelor laboratorium technoloog en voorafgaande ervaring in een laboratorium is een pluspunt
• 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
Location: Wilrijk , Antwerp
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 Technical Expert Immunohistochemistry (AD-TEX)
Department: Assay Development, Histopathology
Based in
Wilrijk, Antwerp (Belgium)
Major responsibilities
Background and competences
Job Related competences
Personal Competences
We offer an exciting and challenging full-time position in a multinational environment where customer focus and innovation are key business values. You will join a global CRO where your expertise matters and contributions can be felt. You will receive thorough on-the-job-training.
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 ISO13485.
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