Assay Development Scientist - Genomics Services (Hybrid)

caprion; Antwerpen; Hybride; EUR 60 000 - 90 000; Plein temps

Avantages offerts par ce poste

Hybrid work schedule

Résumé du poste

CellCarta is seeking an Assay Development Scientist for its Genomics Services team in Belgium. You will lead development, validation and implementation of high-quality qPCR, dPCR, and NGS assays for use in clinical trials, leveraging DNA/RNA technologies.

The role requires at least 3 years in assay development within regulated environments, strong molecular genetics background, and hands-on lab experience. This hybrid position involves three onsite days per week in Wilrijk, Antwerp.

Qualifications

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

Responsabilités

• 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

Connaissances

Molecular genetics

Genomics technologies

qPCR

dPCR

NGS

English proficiency

MS Office

Data analysis

Formation

Master’s degree or PhD in Life Sciences

Outils

qPCR

dPCR

NGS

Description du poste

Assay Development Scientist - Genomics Services (Hybrid)

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

Working Conditions

• Full-time, permanent position with a hybrid work schedule requiring a minimum of three days onsite per week

About CellCarta

CellCartais 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!

The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.

CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact [e-mail].