Assay Development Scientist

il y a 1 jour

Antwerpen, Flandre, Belgique TN Belgium Temps plein
Client:

CellCarta

Location:

Antwerp, Belgium

Job Category:

Other

EU work permit required:

Yes

Job Reference:

64a3b26ac4f0

Job Views:

4

Posted:

03.03.2025

Expiry Date:

17.04.2025

Job Description:

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

  1. Design new assays and map-out validation experiments according to the intended use of the assay.
  2. 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.
  3. Prepare project related documentation (development and validation plan), including literature study.
  4. Compile data for presentations and reports to share with internal and external stakeholders.
  5. 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.
  6. Maintain oversight of the project's financial status.

Education

Master's Degree in Life Sciences (preferably Biology, Biomedical Sciences, Bioengineering, Pharmaceutical Sciences, Biochemistry).

Main Requirements

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

Working Conditions

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.

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