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 expand 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.
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We are currently recruiting: Assay Development Scientist
Department: Genomics Services
Based in
Wilrijk, Antwerp (Belgium)
Major responsibilities
As an Assay Development Scientist within our Genomics Services team, you will be responsible for the implementation, development and validation of high-quality qPCR, dPCR and NGS assays for use in clinical trials utilizing state of the art RNA and DNA technologies. This will entail:
- Manage, plan, create and execute complex technical and laboratory studies for small teams, writing protocols, reviewing and approving documents within design control procedures.
- Conduct laboratory procedures to support the development or implementation of assays across different workflows such as qPCR, dPCR, NGS and high throughput platforms.
- Troubleshoot and perform technical interpretation of data, evaluate and document studies, analyze and present results in written reports.
- Work collaboratively with team members and colleagues from other functions to ensure projects are delivered safely, effectively and efficiently to the required quality and regulatory standard in a timely manner.
- Develop and present data collected for internal and external projects.
- Prepare and lead departmental and client meetings.
Qualifications and skills
- Master or PhD in Life Sciences (preferably Biology, Biomedical Sciences, Bioengineering, Pharmaceutical sciences, Biochemistry) or equivalent trough experience with minimum 3 years of relevant professional experience in a strongly regulated environment.
Job related competences
- Solid basis in Molecular genetics and genomics technology is essential.
- Experience with assay development using qPCR or dPCR or NGS is required.
- Experience in working in a regulated environment (ISO13485) is a plus.
- Strong computer skills and significant experience with Microsoft Excel, Powerpoint and Word are required.
Personal competences
- Proven organisational skills, self-motivation, accountability and attention to detail.
- Able to manage and prioritize multiple projects.
- Strong troubleshooting, data analysis and interpretation skills.
- Flexible, social, diplomatic, a team player, inspirational and a strong communicator.
- Fluent in English both written as well as spoken.
- Result oriented, creative and analytical thinker with a problem-solving mindset.
- Eager to learn/assimilate novel concepts.
What we can 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
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