Assay Development Scientist (Histopathology)

Assay Development Scientist (Histopathology)

Are you looking to make your next career move? CellCarta, a Contract Research Organization, is hiring an Assay Development Scientist to join our dynamic team. As an Assay Development Scientist, you will have the opportunity to use your expertise and skills 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 assay development unit is responsible for the optimization and validation of high quality (single and multiplex) IHC, RISH, FISH, and CTC assays for use in clinical trials. As an Assay Development Scientist, you will collaborate with the assay development team and other internal stakeholders (such as the laboratory, QA, RA, and Clinical sample testing unit) during all stages of the development and validation process.

Responsibilities

More specifically, you will participate in the following:

• Design new assays and map-out validation experiments according to the intended use of the assay. This will not involve any experimental activities in the lab, but you will have to assure a proper transition of the scheduled experiments to the laboratory (i.e. compilation of structured and transparent experimental protocols, knowledge of the technology and platforms);
• Perform data analysis (e.g. analysis of immunohistochemically stained images, defining regions of interest in (tumor) tissue sections, and qualitatively evaluating staining and overall assay performance, etc.) through the various phases of development under the supervision of the Senior Assay Development Scientist;
• Prepare project related documentation (development and validation plan), including literature study;
• Compile data for presentations and reports to share with internal and external stakeholders;
• Communicate with internal stakeholders to update the progress of the assay development, to clarify problems, and discuss the options to deliver high-quality assays within the set timelines;
• Maintain oversight of the project's financial status.

Education

• Professional Bachelor (Medical, Pharmaceutical or Biomedical Laboratory Technologies, Biochemistry), or Bachelor’s or Master’s Degree in Life Sciences (preferably Biology, Biomedical Sciences, Bioengineering, Pharmaceutical Sciences, Biochemistry).

Main Requirements

• Profound knowledge of immunohistochemistry and other related techniques and/or histopathology is preferred;
• Strong background in histology/histopathology and/or microscopy is an asset;
• Strong computer skills and significant experience with Microsoft Excel, PowerPoint and Word are required;
• Experience with image analysis software (Visiopharm, HALO, etc.) and digital imaging is a plus;
• Advanced command of the English language, along with outstanding writing and communication skills;
• Ability to rapidly learn and apply knowledge in previously unfamiliar areas;
• Highly organized and able to manage and prioritize multiple projects;
• Methodically and meticulously demonstrate a high quality of work, including accuracy, timeliness, professionalism, and thoroughness;
• Analytical, problem-solving, and result-oriented mindset;
• Social, diplomatic, a team player, and a strong communicator.

• Full-time, permanent position with a hybrid work arrangement, requiring 2-3 days of onsite attendance.

Benefits

We offer a wide range of benefits including:

• A dynamic and rapidly changing global environment that allows for personal growth;
• Training and personal development in a variety of technical and interpersonal areas;
• Career opportunities as the company grows quickly;
• A healthy work-life balance with onsite and remote working;
• A forward-thinking company that is fit for the future;
• A competitive salary and benefits package;
• An excellent team to work with.

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 facilities located in Canada, USA, Belgium, Australia, and China.

Joining CellCarta means working with 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! 

Join us as we make an impact on patient therapy!

The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.

CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact [email protected].