Geneticist - Blueprint Genetics Oy - Remote - Global

Are you an expert in human genetics and inherited diseases? Do you have the ambition to utilize your experience in genetic interpretation whilst being among the pioneers of the molecular era of medicine? Are you passionate about helping patients? If you answered “yes,” you might be the person we are looking for! Blueprint Genetics, a Quest Diagnostics company, is on a mission to bring world-class genetic knowledge to mainstream healthcare. We are a team of experienced professionals with diverse backgrounds, who share a passion for helping patients and families affected by inherited disorders. We work with hundreds of clinics around the globe and the quality of our interpretation has been praised by many of the world’s best medical centers. To support our growth, we are looking for Geneticists to join our Clinical Interpretation team in Helsinki and across Europe. The position is based out of our Helsinki office, but we offer the opportunity to work remotely for a person located in Finland, Sweden, Germany or Spain. We are looking for those who want to make a difference. In this position, you will have the opportunity to work with an experienced and motivated geneticist team that places great value in high-class clinical interpretation. We have a diverse genetic testing portfolio, including over 220 panels across 14 medical specialties, whole exome sequencing, approximately 3,900 single genes, and targeted variant analysis. Your daily work will entail analyzing the genetic data with our in-house developed interpretation tool and writing the test results into high-quality written clinical statements. Interpretation of the data requires the use of several databases, genetic tools, and understanding of how the clinical history of the patient matches with the findings. In more challenging cases, you are supported by a group of senior staff with experience on various medical specialties and product categories. Our global and multidisciplinary team of geneticists is a unique group of more than 60 scientists: Geneticists (PhD), Variant Scientists (MSc) and Clinical Laboratory Geneticists. Our team members have an average of more than 13 years of previous scientific experience, several years in clinical diagnostics (per person), and altogether more than 500 peer-reviewed scientific articles published. Thus, you will be supported by a group with extensive experience in the field. We are looking for a person with a patient-first mindset, who is truly motivated to find answers for individuals affected by inherited diseases. You are able to deliver high-quality results independently, and taking responsibility comes naturally to you. At the same time, you are a team player with eagerness to work towards a common goal. You are enthusiastic about keeping up with the most recent scientific findings and developing your expertise. You work efficiently under pressure in a fast-paced production environment, and you adjust effortlessly to changes and evolving situations. Requirements for the position: PhD in Genetics or Molecular Medicine, or Clinical Laboratory Geneticist degree in Clinical Molecular Genetics / Laboratory Genetics and Genomics is required. Excellent understanding of human genetics, inheritance models and inherited human diseases, and the ability to understand medical terminology and learn clinical aspects of the diseases. Uncompromised attention to detail. In practice, this means that an analytical, critical and systemic approach, as well as ability to follow rules, is needed to maintain coherent variant classifications throughout the team and the high quality of the reports. Excellent verbal and written skills in English are a necessity. You are located in Finland, Sweden, Germany or Spain. The following qualities are seen as advantages: Knowledge of current genomic information and variant databases, in addition to experience in NGS methods. Research or clinical experience in interpreting genetic test results utilizing NGS, Sanger sequencing and other methods. Experience in whole exome or whole genome analysis. Understanding of how variants are classified. What we offer: The opportunity to work for a company that makes a real difference – Blueprint Genetics has a clear and motivating purpose to improve the lives of patients and families affected by inherited diseases and this commitment is something our Clinical Interpretation team takes great pride in. A positive, open, and international work environment with great people from different fields of expertise. We are a team of close to 250 experienced professionals, who collaborate to drive genetic knowledge forward. How to apply: If you fulfil all the requirements for the position and are interested to join our team, please submit your application and CV at the latest on June 16, 2026. Please note that the interviews will be started as soon as we identify potential candidates, which means that they can be started already during the application period. We hope to hear from you soon! If you have any further questions about the position you can turn to our Sr. Genetics Director Tiia Kangas-Kontio by email tiia.kangas-kontio@blueprintgenetics.com. Who we are: Blueprint Genetics is a Quest Diagnostics company. Quest Diagnostics, A Fortune 500 company, is the world’s leading provider of diagnostic information services. www.questdiagnostics.com