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
Location: Lake Forest , CA
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
Mosaic Laboratories is in search of an Associate Project Manager based in Lake Forest, CA. As a member of our team, you will provide support for multiple projects. You will help the project managers ensure project objectives are met, completed on time, on budget, and in accordance with the signed protocols. You will provide appropriate updates to the client, sit in on client calls, and support client needs.
This is a full-time day shift position working Monday – Friday from 9:00 AM-5:30 PM.
Responsibilities
Education
Requirements
Physical Demands and Work Environment
While performing the duties of this job, the employee is regularly required to use hands and fingers to operate scientific equipment and reach with hands and arms. The employee is frequently required to stand and sit. The employee is occasionally required to walk, talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision requirements of this job include the demonstrated ability to differentiate between red and green by passing the color blindness test, close vision, and the ability to adjust focus.
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:
Location: Lake Forest , CA
Job Summary:
CellCarta is in search of an Assay Development Manager based out of our Lake Forest, CA laboratory. As a leader within our Assay Development team, you will be responsible for providing direction over our assay development projects, coordinating staff, and partnering with our scientific teams to achieve results.
Ideal candidates will have hands-on experience with assay development, optimization, and validation. They will have experience managing a large number of complex projects and providing guidance and oversight to employees.
Responsibilities:
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: Lake Forest , CA
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 ensures 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
The Scanning Assistant I is responsible for scanning stained slide-mounted specimens, performing QC review of scanned images, coordinating the completion of scanning requests from departmental leadership and project management, monitoring and performing preventative maintenance on equipment, and performing various technical laboratory or administrative duties as necessary.
Responsibilities
Education
Benefits
We offer a wide range of benefits including:
Physical Demands and Work Environment
While performing the duties of this job, the employee is regularly required to use hands and fingers to type and file and to reach with hands and arms. The employee is frequently required to stand and sit. The employee is required to walk, talk, see, and hear. The employee must occasionally lift and/or move up to 20 pounds.
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. Monday - Friday 9:00am - 5:00pm.
Responsibilities
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: , (Multiple States)
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
We are seeking a driven, high-energy, early-in-career sales professional who is motivated to drive new business and uncover opportunities with our rapidly growing US commercial team.
The Inside Sales Specialist (ISS) will be responsible for driving new business by qualifying leads and prospecting external customers (pharma and biotech partners) for a potential new business focused on assay development, validation, and clinical sample analysis projects. The ISS will work with our talented commercial team to research and build a pipeline, identify target accounts, and help develop efficient methods of outreach to external customers (pharma and biotech partners) for potential new business. You will be assigned to support a region and the Business Development team that sell CellCarta’s services and will support the implementation of sales campaigns and strategies for accounts in the assigned territory.
This is a key individual contributor role focusing on contacting prospective buying influences across the biopharma industry and is directly involved in account identification and business growth across our customized biomarker testing solutions portfolio.
Our ideal candidate is a hardworking and focused analytical thinker, with strong communication skills, attention to detail, a passion for sales, with an academic or professional background in Immunology. You must enjoy working independently, be self-motivated, and love to learn about the latest scientific developments and technologies delivering precision medicine to patients.
Responsibilities
Education
Requirements
Benefits
We offer a wide range of benefits including:
Location: , (Multiple States)
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
We are seeking a driven, high-energy, early-in-career sales professional who is motivated to drive new business and uncover opportunities with our rapidly growing US commercial team.
The Inside Sales Specialist (ISS) will be responsible for driving new business by qualifying leads and prospecting external customers (pharma and biotech partners) for a potential new business focused on assay development, validation, and clinical sample analysis projects. The ISS will work with our talented commercial team to research and build a pipeline, identify target accounts, and help develop efficient methods of outreach to external customers (pharma and biotech partners) for potential new business. You will be assigned to support a region and the Business Development team that sell CellCarta’s services and will support the implementation of sales campaigns and strategies for accounts in the assigned territory.
This is a key individual contributor role focusing on contacting prospective buying influences across the biopharma industry and is directly involved in account identification and business growth across our customized biomarker testing solutions portfolio.
Our ideal candidate is a hardworking and focused analytical thinker, with strong communication skills, attention to detail, a passion for sales, with an academic or professional background in Immunology. You must enjoy working independently, be self-motivated, and love to learn about the latest scientific developments and technologies delivering precision medicine to patients.
Responsibilities
Education
Requirements
Benefits
We offer a wide range of benefits including:
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: Montreal , QC
Quality Improvement Specialist
Looking for a career that makes a difference? CellCarta, a cutting-edge biotech company, is seeking a Quality Improvement Specialist to join our dynamic team. As a Quality Improvement Specialist at CellCarta, you'll have the opportunity to use your expertise and passion for quality to ensure that our services meet the highest industry standards. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being. Apply today and take the first step towards an exciting new career with CellCarta!
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
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 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 11 facilities located in Canada, USA, Belgium, Australia, and China.
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 11 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 11 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: Wilrijk , Antwerpen
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
Quality Improvement Specialist
Looking for a career that makes a difference? CellCarta, a cutting-edge biotech company, is seeking a Quality Improvement Specialist to join our dynamic team. As a Quality Improvement Specialist at CellCarta, you'll have the opportunity to use your expertise and passion for quality to ensure that our services meet the highest industry standards. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being. Apply today and take the first step towards an exciting new career with CellCarta!
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
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 11 facilities located in Canada, USA, Belgium, Australia, and China.
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 11 facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
Reporting to the Manager - Sample Reception, the Assistant - Sample Reception is responsible for performing various tasks to support the activities of sample and reagent reception, along with storage, shipment, and disposal.
Responsibilities
Education
Main Requirements
Schedule
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 11 sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
Sous la responsabilité du gestionnaire de la réception des échantillons, l'assistant(e) de la réception des échantillons est chargé(e) d'effectuer diverses tâches pour soutenir les activités de réception des échantillons et des réactifs, ainsi que le stockage, l'expédition et la disposition.
Responsabilités
Formation
Exigences principales
Horaire
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 11 facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
Reporting to the Manager - Sample Reception, the Assistant - Sample Reception is responsible for performing various tasks to support the activities of sample and reagent reception, along with storage, shipment, and disposal.
Responsibilities
Education
Main Requirements
Schedule
What We Offer
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 11 sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
Sous la responsabilité du gestionnaire de la réception des échantillons, l'assistant(e) de la réception des échantillons est chargé(e) d'effectuer diverses tâches pour soutenir les activités de réception des échantillons et des réactifs, ainsi que le stockage, l'expédition et la disposition.
Responsabilités
Formation
Exigences principales
Horaire
Ce que nous offrons
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 Finance & Accounting Centre team, this role reports to the Director of Finance. The Accounting Associate will be primarily responsible for working cross-functionally with Finance Department team members to prepare monthly Financial Statements. The ideal candidate has an analytical mind, great communication skills, and an understanding of the full accounting cycle. This role is a three month contract with the possibility of becoming permanent.
Key Responsibilities:
Key Responsibilities:
Education and Experience:
What we offer:
Location: Wilrijk , Antwerpen
Warehouse Operations Associate
As a global Research Organization to the biopharmaceutical industry, CellCarta supports pharmaceutical and biotech companies in the research and development of new innovative medicines for the treatment of cancer and immune disorders.
The Logistics Division of CellCarta, where this new position is located, is a trusted provider of sample collection & shipping kits, and sample management services to support laboratory testing.
We are currently looking for an Operations Associate to join our team in the Logistics Division. Based in Wilrijk, Antwerp (Belgium) – work both in an office environment and in the warehouse where kits are assembled for clinical trials and finished products are distributed to various global locations.
The tasks and responsibilities
- Manual picking of supplies
- Custom label printing
- Packing supplies
- Shipping supplies
- Other tasks, as required, to meet deliverables.
Profile
- Ability to learn and adapt to new processes.
- Competent in Microsoft office.
- Teamwork, effective communication and customer focus are the core competencies
- Reliable and have an eye for quality
- Has a sense of urgency to meet deadlines.
- Willingness to roll up your sleeves.
- English speaking, Dutch is an asset
- Work experience in the logistics sector (warehouse employee, order picker, packer, production) or willing to learn.
- High school diploma or equivalent; Bachelor’s degree or equivalent is an asset.
- Certificate to use a reach truck is an asset
Offer
- Full-time 38 hours/week (no weekends nor shift).
- Open-ended contract.
- You will get a competitive salary and extra-legal benefits (e.g. meal vouchers, insurance)
- To help keep the home/work balance, we give you extra holidays on top of the legal holidays.
- Working within a small, social, enthusiastic team
- On the job training
- Many opportunities to grow
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, The Assistant Production Manager is responsible for the management and oversight of the operations department. Reporting to the Production Manager, the incumbent in this role improves operational management systems and is responsible for production KPI’s.
Key Responsibilities
Qualifications
Physical Demands
Working Conditions
Other
Although the duties outlined constitute the bulk of what a Assistant 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: Montréal , QC
À propos de CellCarta
CellCarta est un fournisseur de premier plan de services de laboratoire spécialisés dans la 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, depuis la découverte jusqu'aux essais cliniques de phase tardive. La société opère 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.
Sommaire
Le directeur du développement des essais est responsable du développement des essais de cytométrie de flux qui répondent à l'objectif visé dans le cadre des essais cliniques. Il gère et encadre une équipe de scientifiques et d'assistants de recherche pour le développement d'essais personnalisés, la mise en place de panels standard, la caractérisation des essais et la validation de l'adéquation des études exploratoires, et fournit des conseils pour une conception efficace des essais et le dépannage des problèmes techniques rencontrés au cours du développement. Ils assurent un leadership scientifique/technique au sein de l'équipe de développement, ainsi que de l'équipe scientifique (scientifiques principaux), au sein de l'organisation CellCarta, lors de réunions scientifiques et avec les clients de CellCarta. Ils sont également chargés de veiller à ce que les essais développés et caractérisés dans le cadre du développement soient suffisamment robustes pour atteindre le niveau d'excellence opérationnelle requis. Il dirige l'équipe de développement en tant qu'unité "SWAT" pour les tests déployés par l'équipe de surveillance immunitaire, il est également responsable de représenter CellCarta lors de réunions scientifiques et de fournir un soutien au développement commercial au niveau scientifique/technique. Le directeur du développement des essais peut être amené à diriger ou à participer à la mise en œuvre de nouvelles technologies ainsi qu'à améliorer les protocoles de cytométrie en flux existants ou à en mettre en œuvre de nouveaux.
Responsabilités
Conditions particulières du poste actuel
Éducation
Expérience et compétences requises
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. We offer our services on a global scale through our laboratories in Canada, USA, Belgium, China and Australia.
Summary
The Global Revenue Accounting Manager is primarily responsible for revenue recognition under ASC 606 and US GAAP for CellCarta’s complex customer contracts and revenue streams. This role reports directly to the Global Controller and has direct responsibility for monthly accounting, reconciliation and reporting activities with a focus on driving improvement initiatives and across functional processes related to revenue and backlog reporting, and forecasting.
The Revenue Accounting Manager leads harmonization of global revenue accounting processes and reporting, partnering with finance, lab operations, program management and commercial teams within our global business.
Main Responsibilities
Education
Experience and Skills Required
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 Director of Assay Development is responsible for the development of flow cytometry assays that meet the intended purpose in the scope of the clinical trial(s). They manage and mentor a team of scientists and research assistants for the development of custom assays, standard panel set-up, assay characterization and fit-for-purpose validation of exploratory studies, as well as provides guidance for effective testing design and troubleshooting of technical issues encountered in development. They provide scientific/technical leadership within the development team, as well as the scientific team (principal scientists), within CellCarta organization, at scientific meetings and with CellCarta customers. They are responsible also to ensure that the assays developed and characterized in development are robust enough to meet the required operational excellence level. They lead the development team as a "SWAT" unit for assays deployed by the immune monitoring team, they are equally responsible to represent CellCarta at scientific meetings and to provide support to business development at the scientific/technical level. The Director of Assay Development may be required to lead or participate at the implementation of new technologies as well as enhance existing or implement new flow cytometry protocols.
Responsibilities
Special Conditions of the Current Position
Education
Experience and Skills Required
Location: Montréal , QC
À propos de CellCarta
CellCarta est un fournisseur de premier plan de services de laboratoire spécialisés dans la 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, depuis la découverte jusqu'aux essais cliniques de phase tardive. Nous offrons nos services à l'échelle mondiale grâce à nos laboratoires au Canada, aux États-Unis, en Belgique, en Chine et en Australie.
Sommaire
Le/la Gestionnaire Global, Comptabilité des Revenus est principalement responsable de la comptabilisation des revenus en vertu de l'ASC 606 et des US GAAP pour les contrats clients complexes et les flux de revenus de CellCarta. Ce rôle relève directement du contrôleur mondial et a la responsabilité directe des activités mensuelles de comptabilité, de rapprochement et de reporting, en mettant l'accent sur la conduite d'initiatives d'amélioration et sur l'ensemble des processus fonctionnels liés aux rapports sur les revenus et le carnet de commandes, ainsi qu'aux prévisions.
Le/la Gestionnaire Global, Comptabilité des Revenus dirige l'harmonisation des processus de comptabilité des recettes et de reporting au niveau mondial, en partenariat avec les équipes financières, les opérations de laboratoire, la gestion des programmes et les équipes commerciales au sein de notre entreprise mondiale.
Principales responsabilités
Éducation
Expérience et compétences requises
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 11 sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
Sous la responsabilité du coordinateur du contrôle de la qualité, le stagiaire réviseur de la documentation effectuera des activités de contrôle de la qualité liées aux projets qui lui sont assignés.
Responsabilités
Formation
Expérience et compétences requises
Horaire
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 11 facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
Reporting to the Coordinator, Quality Control, the Documentation Reviewer Intern will perform quality control activities which are linked to assigned projects.
Responsibilities
Education
Required Experience and Skills
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 100 employees in its 11 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: 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 11 facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
CellCarta is seeking a Sample Logistics Technician to work closely with the Operations teams for the logistics and tracking of international clinical trial shipments.
Responsibilities
Education
Main Requirements
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 11 sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
CellCarta recherche un(e) technicien(ne) en logistique des échantillons pour travailler en étroite collaboration avec les équipes des opérations pour la logistique et le suivi des expéditions internationales d'essais cliniques.
Responsabilités
Formation
Exigences principales
Location: Lake Forest , CA
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
The Scientific Director, Histopathology Operations, is responsible for the oversight and technical conduct of assay development, and preclinical, and clinical trial studies, in accordance with standard operating procedures.
Responsibilities
Education
Requirements
Physical Demands and Work Environment
While performing the duties of this job, the employee is regularly required to use hands and fingers to operate scientific equipment and reach with hands and arms. The employee is frequently required to stand and sit. The employee is occasionally required to walk, talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision requirements of this job include the demonstrated ability to differentiate between red and green by passing the color blindness test, close vision, and the ability to adjust focus.
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:
Location: Fremont , CA
Immunology Intern, R&D
Are you a senior in college or a recent graduate with your Bachelors? Are you a curious and driven individual looking to kickstart your career in the world of biotech and immunology? We are a leading biotech company searching for an enthusiastic and motivated Research and Development Intern to join our innovative team. As an intern, you will have the opportunity to work alongside industry experts and contribute to cutting-edge research and development projects that have the potential to make a meaningful impact on society. Don't miss out on this exciting opportunity to jumpstart your career in biotech - apply today!
Job Summary
The Immunology Intern supports drug discovery across the biotechnology industry by providing support and assisting those performing complex cellular assay services on samples from patients, healthy donors, and various animal species. Most assays involve analyzing immune cells by flow cytometry to evaluate pre-clinical therapeutics, biomarkers, or drug activity in patients. The objective is to give the intern hands-on laboratory work and documenting protocols. Additional time spent assisting in the planning of experiments, analyzing data, and presenting results as experience is gained.
Flow cytometry is a technology that rapidly analyzes single cells and is a powerful tool that has applications in multiple disciplines such as immunology, virology, molecular biology, cancer biology and infectious disease monitoring. Flow cytometry allows for the simultaneous characterization of mixed populations of cells from blood and other samples. Flow cytometry is a very effective tool for studying the immune system.
Responsibilities
Education
Experience and Skills
Position Information
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: 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 11 sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
CellCarta est à la recherche d'un(e) technicien(ne) - Gestion des échantillons pour travailler en étroite collaboration avec les équipes des Opérations, à recevoir et gérer les échantillons ainsi que les réactifs et la marchandise.
Responsabilités principales
Formation
Exigences principales
Horaire de travail
Ce que nous offrons
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 11 facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
Reporting to the Group Leader, Sample Management Reception, the Sample Management Technician is responsible for working closely with the operations teams, receiving, and managing samples as well as reagents and materials.
Responsibilities
Education
Main Requirements
Work Schedule
What We Offer
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.
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 700 employees in its nine facilities located in Canada, USA, Belgium, Australia, and China.
Summary
Clinical Logistics is currently seeking a motivated candidates to fill the role of Operations Associate. This position is responsible for manual tasks within the operations and shipping area and requires the candidate to be on their feet most of the day. In addition, the candidate is expected to uphold Clinical Logistics quality standards, follow approved instructions, controlled processes and good documentation practices.
Duties and Responsibilities:
Requirements:
Additional Requirements:
Working Conditions:
Compensation and Benefits:
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 11 facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
The In-Life Documentation Reviewer will perform in-life review of experimental documentation in the laboratory based on approved driving documents and SOPs.
Responsibilities
Education
Required Experience and 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 1,000 personnes dans ses 11 sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
Le réviseur de documentation (In-Life) effectuera la révision en temps réel de la documentation expérimentale dans le laboratoire, sur la base des documents de conduite et des SOPs approuvés.
Responsabilités
Formation
Expérience et compétences requises
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 11 facilities located in Canada, USA, Belgium, Australia, and China.
Position Summary
The Documentation Reviewer will perform quality control activities which are relevant to his/her field of expertise and linked to assigned projects.
Responsibilities
Education
Required Experience and 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 1,000 personnes dans ses 11 sites situés au Canada, aux États-Unis, en Belgique, en Australie et en Chine.
Résumé du poste
Le réviseur de documentation effectuera des activités de contrôle de la qualité en rapport avec son domaine d'expertise et avec les projets qui lui sont assignés.
Responsabilités principales
Formation
Expérience et compétences requises
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 11 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: 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) – 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 Specialist reports to the Team Manager End-User, Cloud and Platform Services Europe-Asia.
Main responsibilities
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: 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 11 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
Bio Sample Shipping Clerk
Join the cutting-edge world of biotechnology as a Bio Sample Shipping Clerk! This entry-level role is your ticket to join a large and innovative company that is shaping the future of healthcare. You'll be a vital part of the team, ensuring that clinical trial shipments are picked up, tracked, and delivered safely and accurately. Be a part of a company that values its employees and encourages growth and development. Don't miss out on the chance to work for a company at the forefront of biotech innovation. Apply today!
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
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: 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: 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
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 1,000 personnes dans ses 11 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: Naperville , IL
Laboratory Operations 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 Operations 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: 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
RESEARCH PROJECT LEAD
Are you a dynamic individual with a passion for driving projects to success? We are seeking a highly motivated Project Lead to join our biotech company and lead innovative projects. Your extensive experience in flow cytometry, combined with your deep understanding of immunology, will be critical in delivering breakthrough solutions that have a lasting impact on human health. If you have a track record of leading projects and a drive to push the boundaries of what's possible, we want to hear from you. Join us and make a real difference in the world!
Position Summary
The Research 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:
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
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
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
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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 1, 000 personnes dans ses 11 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
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: 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: 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: antwerp , Antwerp
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 , Antwerp
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 Clinical Data Manager to join the Data Management & Bio-Informatics department in Wilrijk Belgium.
If you are organized, analytically minded, possess a solid technical background, have a passion for IT and will thrive in our dynamic, high complexity environment, this might just be the role you are looking for.
Required education
A Master’s degree in Sciences, Biomedical Sciences, Pharmaceutical Sciences, Medical Biology, Medicine or equivalent by experience considered as minimum of 5 years of experience in Clinical Data Management. Having obtained a PhD is considered a plus.
Major responsibilities
Qualification and Skills
It's great, but not required, if you have experience with:
We offer an exciting and challenging position in a multinational environment where customer focus and innovation are key business values. 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 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