Assay Development Scientist - Genomics Services

CellCarta

Wilrijk or Antwerp, Belgium

Are you a scientist with expertise in molecular genetics and genomics technologies? Join CellCarta's Genomics Services team as an Assay Development Scientist and contribute to the advancement of innovative genomic assays supporting clinical trials.

In this role, you will lead technical studies, analyze and troubleshoot data, and collaborate with cross-functional teams to deliver high-quality solutions in a regulated environment. If you are a self-motivated, detail-oriented scientist with a passion for innovation and problem-solving, we invite you to join our dynamic team in Wilrijk, Antwerp.

Summary

As an Assay Development Scientist within our Genomics Services team, you will be responsible for the development, validation, and implementation of high-quality qPCR, dPCR, and NGS assays for use in clinical trials, leveraging state-of-the-art RNA and DNA technologies.

Responsibilities

Manage, plan, and execute complex technical and laboratory studies; write protocols and review and approve documentation in accordance with design control procedures
Perform laboratory activities supporting the development, validation, and implementation of assays across multiple workflows
Troubleshoot, interpret, and analyze data; evaluate and document studies; and present results in technical reports
Collaborate with internal teams and cross-functional stakeholders to ensure projects are delivered safely, efficiently, and in compliance with quality and regulatory requirements
Prepare and present scientific data for internal and external projects
Organize, lead, and participate in departmental and client meetings

Education

Master’s degree or PhD in Life Sciences (preferably Biology, Biomedical Sciences, Bioengineering, Pharmaceutical Sciences, or Biochemistry) or an equivalent discipline

Main Requirements

Minimum of 3 years of relevant experience in assay development or a related role within a highly regulated environment
Strong foundation in molecular genetics and genomics technologies
Hands-on experience in assay development using qPCR, dPCR, and/or NGS technologies
Experience working in a regulated environment (ISO 13485) is considered an asset
Proficiency with Microsoft Office applications, particularly Excel, PowerPoint, and Word
Excellent problem-solving and decision-making skills
Results-oriented, analytical, and creative thinker with a proactive approach
Strong organizational skills with the ability to manage multiple priorities and projects simultaneously
High level of accountability and attention to detail
Strong troubleshooting, data analysis, and interpretation skills
Collaborative, adaptable, and diplomatic team player with excellent communication and interpersonal skills
Fluent in English, both written and spoken
Demonstrated eagerness to learn and apply new concepts and technologies