Associate Assay Development Scientist

**Associate Assay Development Scientist (Histopathology)**

**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**
- Assist the Assay Development team throughout all phases of a project (e.g., start-up, experimental design, scheduling, tracking progress of development and validation experiments, evaluating immunohistochemically stained images, data analysis, and preparing reports for presentation and/or documentation in a finalized format). This role does not include hands-on experimental work in the lab, but you will be responsible for ensuring a smooth transition of scheduled experiments to the laboratory;
- Carry out tasks under the supervision and guidance of senior staff;
- Engage proactively with internal stakeholders to ensure clear, timely, and transparent communication;
- Anticipate potential issues, provide regular updates, and collaborate effectively to meet project-specific objectives;
- Ensure compliance with relevant quality and regulatory standards for the intended use.

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

**Main Requirements**
- Basic knowledge of histology and (automated) immunohistochemical techniques;
- 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;
- Advanced command of the English language, along with outstanding writing and communication skills;
- Excellent organizational skills, including time management, attention to detail, and the ability to prioritize tasks efficiently;
- 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.

**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. We make a difference in the lives of patients around the world

**Join us as we make an impact on patient therapy**

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