Assay Development Scientist - Genomics Services

Assay Development Scientist - Genomics Services

Are you a dedicated scientist with expertise in molecular genetics and genomics technology? Join CellCarta's Genomics Services team as an Assay Development Scientist and contribute to the development, validation, and implementation of cutting-edge qPCR, dPCR, and NGS assays for clinical trials.

In this role, you will manage and execute technical laboratory studies, troubleshoot data, and collaborate with cross-functional teams to ensure the successful and timely delivery of projects to regulatory standards. Your strong foundation in molecular genetics, along with your experience in qPCR, dPCR, or NGS assay development, will be invaluable in this role. If you're a self-motivated, detail-oriented scientist with a passion for innovation and problem-solving, we invite you to be part of our dynamic team in Wilrijk, Antwerp.

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.

More specifically, you will participate in the following:

• 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;
• 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.

Education & Experience:

• Master's or PhD in Life Sciences (preferably Biology, Biomedical Sciences, Bioengineering, Pharmaceutical Sciences, Biochemistry) or equivalent, with a minimum of 3 years of relevant professional experience in a strongly regulated environment.

Competencies & Requirements:

• Solid foundation in molecular genetics and genomics technologies is essential;
• Experience with assay development using qPCR, dPCR, or NGS is required;
• Experience working in a regulated environment (ISO 13485) is a plus;
• Strong computer skills and significant experience with Microsoft Excel, PowerPoint, and Word are required;
• Demonstrated excellent problem-solving and decision-making abilities;
• Results-oriented, creative, and analytical thinker with a proactive mindset;
• Proven organizational skills, self-motivation, accountability, and attention to detail;
• Able to manage and prioritize multiple projects effectively;
• Strong troubleshooting, data analysis, and interpretation skills;
• Flexible, sociable, diplomatic, a team player, inspirational, and a strong communicator;
• Fluent in English, both written and spoken;
• Eager to learn and assimilate new concepts.

Working Conditions:

• Based in Wilrijk, Antwerp (Belgium), with a hybrid schedule of three days onsite.

Benefits:

• A competitive salary and benefits package;
• 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 forward-thinking company that is fit for the future;
• 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!