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Scientist, Diagnostic Assay Development & Design Control
RAB DiagnosticsCompany Description Rab Diagnostics is a biomarker development company focused on oncology, specializing in Antibody-Drug Conjugates (ADCs). Using the proprietary RabCANCER platform and expertise in intracellular drug trafficking, the company delivers mechanism-driven insights that accelerate drug development and support precision medicine. Rab Diagnostics translates preclinical discoveries into clinical impact by creating robust research tools and diagnostic kits. Founded on world-class science at Oslo University Hospital and headquartered in Oslo, Norway, the company values scientific rigor and collaborative partnerships. Rab Diagnostics works with biopharmaceutical partners worldwide to advance precise and effective cancer therapies for patients.
Role Description The Scientist, Diagnostic Assay Development & Design Control is a full-time, hybrid role based in Oslo, Norway, with flexibility for some work from home. This role involves planning, developing, and optimizing diagnostic assays that support oncology-focused ADC programs, including design, validation, and implementation of biomarker tests. Day-to-day responsibilities include conducting laboratory experiments, documenting protocols and results, performing data analysis, and contributing to design control files and quality documentation. The scientist will collaborate with R&D, quality, and external partners to ensure assays meet scientific, regulatory, and GMP-related requirements. The role also includes preparing technical reports, supporting technology transfer, and participating in cross-functional project meetings to align diagnostic solutions with clinical and commercial needs.
Qualifications
Role Description The Scientist, Diagnostic Assay Development & Design Control is a full-time, hybrid role based in Oslo, Norway, with flexibility for some work from home. This role involves planning, developing, and optimizing diagnostic assays that support oncology-focused ADC programs, including design, validation, and implementation of biomarker tests. Day-to-day responsibilities include conducting laboratory experiments, documenting protocols and results, performing data analysis, and contributing to design control files and quality documentation. The scientist will collaborate with R&D, quality, and external partners to ensure assays meet scientific, regulatory, and GMP-related requirements. The role also includes preparing technical reports, supporting technology transfer, and participating in cross-functional project meetings to align diagnostic solutions with clinical and commercial needs.
Qualifications
- Strong laboratory skills, including hands-on experience with diagnostic assay development and biomarker testing.
- Proven experience in Research and Development (R&D), with the ability to design, execute, and troubleshoot experimental studies.
- Knowledge of Good Manufacturing Practice (GMP) principles and quality systems relevant to diagnostic kit or IVD development.
- Proficiency in data analysis and research, including statistical evaluation, interpretation of complex datasets, and clear reporting of findings.
- Advanced degree (e.g., MSc or PhD) in molecular biology, biotechnology, biochemistry, immunology, or a related life science field.
- Experience with design control, assay validation, and documentation in a regulated or quality-focused environment.
- Familiarity with oncology, biomarkers, or ADC-related technologies is highly beneficial.
- Strong written and verbal communication skills in English, with the ability to collaborate effectively in interdisciplinary teams.
- Ability to work independently, manage multiple projects, and adapt to a dynamic, innovation-driven environment.