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CellCarta

CellCarta

cellcarta.com

3 Jobs

708 Employees

About the Company

As a global leader in precision medicine testing services, we partner with our clients to address the most complex biomarker and bioanalytical challenges and deliver highly customized testing solutions. With facilities located in Canada, United States, Belgium, Australia and China, CellCarta provides the expertise needed locally to support global clinical trials.

CellCarta offers access to integrated analytical platforms in immunology (immune monitoring), histopathology, proteomics and genomics, as well as digital pathology/AI and sample management, logistics and kitting services.

At CellCarta we are experts at assessing the immune system, whether in the context of oncology, infectious diseases, or autoimmune diseases. With a proven track record in other therapeutic areas as, such as neurological and metabolic disorders, we handle all human biological specimens and deploy relevant technologies to extract valuable information for research and diagnostic applications. We provide assay development and testing services to support a wide variety of translational research, clinical trials, and diagnostic applications.


Reflecting our commitment to quality, our sites hold the appropriate accreditations to support your regulatory requirements, including CAP, CLIA, ISO15189, ISO27001 and ISO13485.

Listed Jobs

Company background Company brand
Company Name
CellCarta
Job Title
Development Scientist
Job Description
**Job Title:** Development Scientist **Role Summary:** Lead the design, development, and validation of cell‑based, immunoassay, and biochemical assay platforms (e.g., flow cytometry, spectral flow, CyTOF, ELISpot, ELISA, MSD, single‑cell genomics). Serve as a technical and scientific resource for assay teams, ensure compliance with GLP/GCLP, and collaborate cross‑functionally to deliver high‑quality data and reports. **Expectations:** - Deliver R&D projects on schedule and communicate any delays promptly. - Maintain up‑to‑date knowledge of immunology, assay technologies, and regulatory standards. - Produce clear, concise documentation, reports, and presentations for internal and external stakeholders. - Train and mentor laboratory staff on complex methodologies. - Adhere to health‑safety and biosafety (BSL‑1/2) protocols. **Key Responsibilities:** - Lead development and optimization studies for novel assay methods. - Design, execute, and troubleshoot experiments; document all activities per SOPs, GLP, and GCLP. - Perform comprehensive data analysis, interpretation, and generate scientific reports. - Present results to clients and project teams in a professional manner. - Write, review, and maintain assay SOPs and method documentation. - Collaborate with cross‑functional teams to integrate assays into broader projects. - Provide training on advanced techniques (flow cytometry, spectral flow, CyTOF, etc.). **Required Skills:** - Strong expertise in flow cytometry (conventional and spectral), cell sorting, and data analysis of multi‑color panels. - Experience with mass cytometry (CyTOF) and immunoassays (ELISA, MSD) including development and validation. - Proficiency with third‑party flow data analysis software and Microsoft Office. - Knowledge of modern immunology, immune monitoring, and related literature. - Understanding of GLP/GCLP regulations and biosafety requirements. - Excellent written and verbal communication in English (French a plus). - Critical, creative thinker with strong problem‑solving abilities. - Strong interpersonal skills, team orientation, and time‑management capability. **Required Education & Certifications:** - M.Sc. in a pharmaceutical, biotech, or CRO assay development field **or** Ph.D. in life sciences (immunology, virology, molecular biology preferred). - Demonstrated experience in assay development and validation. - Familiarity with GLP/GCLP guidelines; formal certification not mandatory but advantageous.
Montreal, Canada
On site
13-10-2025
Company background Company brand
Company Name
CellCarta
Job Title
Laboratory Technologist, Genomics
Job Description
**Job Title** Laboratory Technologist, Genomics **Role Summary** Conducts advanced molecular laboratory analyses in a genomics setting, supporting research and clinical testing through precise data generation and documentation. **Expectations** Candidates must hold relevant professional education and demonstrate foundational proficiency in molecular lab techniques. Prior experience in a molecular laboratory is advantageous. **Key Responsibilities** - Perform specialized molecular analyses (DNA/RNA extraction) using advanced technologies. - Operate and monitor laboratory equipment, reporting malfunctions promptly. - Maintain and document lab processes in LIMS (Lab Information Management System). - Prepare samples and equipment for testing according to protocol. - Document all laboratory work systematically. - Assist in interpreting and reporting analytical results. **Required Skills** - Proficient in computer use (Word, Excel) and database systems. - Fluency in Dutch and English (oral and written communication). - Effective teamwork and communication abilities. - Accuracy and attention to detail in a structured, ISO-certified environment. - Strong documentation and analytical reporting skills. - Flexibility and adaptability in a dynamic research setting. **Required Education & Certifications** - Professional Bachelor’s degree in Medical, Pharmaceutical, Biomedical Laboratory Technology, or Biochemistry. - No specific certifications required.
Antwerp, Belgium
On site
16-10-2025
Company background Company brand
Company Name
CellCarta
Job Title
Proposal Specialist
Job Description
**Job Title:** Proposal Specialist **Role Summary:** Prepare and manage accurate proposals and task orders, coordinate with commercial, client management, and operations teams, and maintain CRM tracking to support sales and service delivery in a contract research organization. **Expectations:** - Deliver high‑quality proposals within tight timelines. - Ensure compliance with customer, quality, and regulatory requirements. - Collaborate effectively across internal and external stakeholders. - Maintain up‑to‑date pricing, legal, and scheduling information. **Key Responsibilities:** - Develop, review, and finalize proposals and Statements of Services for accuracy. - Generate sales price estimates for protocols, bid requests, study revisions, and additions using approved pricing guidelines. - Update and maintain the CRM system for proposal tracking and reporting. - Coordinate with internal (and, when needed, external) stakeholders to complete proposals and meet client needs. - Assist management in monitoring pricing practices for relevance and accuracy. - Ensure all required legal documents are secured and attached. - Work with scheduling/project management teams to identify service dates and support study scheduling. - Support responses to RFIs by liaising with local stakeholders. - Maintain and improve tools such as price lists, budgeting templates, and customer‑specific agreements. - Perform additional related duties as assigned. **Required Skills:** - Strong teamwork and collaboration abilities. - Ability to manage multiple priorities with high attention to detail. - Basic understanding of histopathology, immunohistochemistry, and/or genomics (preferred). - Experience in client services, budget preparation, or CRM usage (preferred). - Effective written and verbal communication skills. **Required Education & Certifications:** - Bachelor’s degree in life sciences, applied sciences, business, or a related field. - No specific certifications required; relevant experience is an asset.
Antwerp, Belgium
Hybrid
06-11-2025