Rarity Bioscience AB jobb

Rarity Bioscience is growing rapidly, with demand for our products higher than ever. To meet this momentum, we are looking for an Field Application Scientist to join our commercial team. This role offers an opportunity to be part of a dynamic and collaborative scale-up environment where science and innovation are at the heart of everything we do. About The Role You will act as the scientific ambassador for our company, empowering researchers and lab professionals to unlock the full potential of our superRCA technology. You will will be key in ensuring customer success, from delivering hands-on training, offering expert guidance, and providing professional technical support.You’ll also collaborate closely with R&D and product management to ensure that real-world customer feedback is translated into meaningful product improvements. Key Responsibilities: Support customer onboarding and provide technical training on our assays and technologies. Act as the primary technical contact for customers, ensuring a smooth implementation and ongoing support. Collaborate closely with R&D to channel customer feedback into product improvements and innovation. Contribute to sales by demonstrating product value, supporting technical evaluations, and participating in customer meetings. Help build scalable workflows, documentation, and best practices for customer success. The role is based at our office in Uppsala Science Park, soon in Uppsala Business Park as we are moving, but will require frequent global traveling. You will report to the Sales Director and become part of a growing commercial team. Calling this opportunity a life-changing journey might be too much, but we can definitely promise dedicated colleagues, an open work culture where collaboration is prioritized in everyday work. Your Profile We are looking for you who is not only technically proficient and customer-focused but also driven by a passion for empowering others. You'll be the expert guiding scientists, helping them excel in their research by serving as their trusted advisor and application coach. Essential Qualifications: MSc or PhD degree in Molecular biology, Biotechnology or related scientific field. Scientifically proficient in Molecular techniques such as; RCA, PCR and Flow cytometry. Previous experience from technical support and/or application science roles in an industry setting is essential. Strong communication and presentation skills. Commercial mindset with a willingness to support sales activities. Proactive, structured, and comfortable working independently as well as in cross-functional teams. Willingness and ability to travel internationally. Why Join Us? At Rarity Bioscience, we believe in fostering a vibrant and collaborative work environment. We have co-located all functions in a modern office in Uppsala Science Park and we regularly organize team get-togethers and off-site events to strengthen our bonds and celebrate our successes. Please do not hesitate to reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ with questions or to get more input why joining, ([email protected], 0763199688). Apply now and become a part of our mission to enable efficinet mutation detection and improve patient outcomes worldwide.

Rarity Bioscience develops ultrasensitive molecular diagnostics based on our proprietary superRCA® technology, enabling detection of rare mutations that standard methods miss. As our portfolio of pharma and clinical collaborations grows, so does our Scientific Services team - and we are now looking for a Senior Scientist to help lead that work. The role You will lead and contribute to scientific collaboration projects in molecular diagnostics and cancer genomics, from initial dialogue to final report. In this role, you combine scientific leadership with involvement across assay development, performance evaluation, sample testing, data interpretation, and customer dialogue. You bring enough scientific depth to be a trusted discussion partner in cancer genetics, while also being practical enough to plan experiments, assess results, provide guidance to junior colleagues, and help move projects from first dialogue to final report or publication. In addition, the role can be expected to include some hands-on lab work to build familiarity with our assays, workflows, and daily operations, with the level of involvement varying depending on project needs. Key responsibilities: Coordinate and execute service projects involving internal laboratory teams, academic researchers, clinical collaborators, and pharmaceutical partners. Plan, perform, analyze, and report laboratory work across oncology, precision medicine, and mutation detection projects. Analyze, interpret, and report experimental and genomic data in relation to clinical data, somatic mutation profiles, and biomarker analyses. Present results to customers and collaborators, and represent Rarity at scientific conferences and meetings. Act as a scientific and technical subject matter expert in assay development, cancer genomics, and molecular diagnostics. Supervise and mentor junior team members in daily operations and project work. Contribute to scientific publications, technical reports, and conference abstracts. Maintain technical documentation in line with Rarity's QMS and applicable regulatory requirements. You will be part of a small, cross-functional team where the distance between a question and a decision is short. The role is based at our office, soon located at Uppsala Business Park, where all functions will be under one roof. Around 30 people today, growing steadily - the kind of place where you know everyone, and where what you do is visible. Who you are You have deep knowledge of cancer genetics, built through years of working with cancer cohorts, patient data, and somatic mutation profiles. You know what variant assessment means in practice, and you can have a real scientific conversation with a pharma R&D team or a clinical researcher without losing the thread. You can lead a project and bring people along with you. You are structured, logical, and not easily derailed but you can change course when the data tells you to. You want to work on something that matters, in a team where no one is afraid of getting their hands dirty and everyone pulls in the same direction. Qualifications: PhD in Molecular Biology, Cancer Biology, Genetics, Genomics, or a related discipline, with approximately five years of relevant experience in academia, a clinical setting, or industry. Strong MSc candidates with equivalent depth will be considered. Solid expertise in cancer genetics and molecular oncology, including experience working with cancer cohorts and interpreting patient and clinical data. Experience with variant calling, variant assessment, and interpretation of NGS data. Hands-on experience with molecular biology techniques such as qPCR, digital PCR, RCA, NGS-based applications, and/or flow cytometry. Experience in assay development, optimization, and validation. Strong data analysis skills — R or equivalent is an advantage. Excellent written and verbal communication in English. Experience presenting scientific results to customers, collaborators, or at conferences. Experience collaborating with pharmaceutical companies or translational research groups is an advantage. Yes, it is a long list. But then again, we are not just any company - we are a team pushing the boundaries of what mutation detection can do, and we are looking for someone who is genuinely excited about that. How to apply If this sounds like the right next step for you, submit your application no later than mid-October. We review applications on a rolling basis, so do not wait too long. Questions about the role or the process? Reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ ([email protected], 0763 19 96 88).

The Role Rarity Bioscience is looking for a hands-on Quality and Regulatory Manager to help transition our innovative molecular diagnostics technology from research use into clinical practice. This is a broad and operational role for someone who enjoys working close to both the science and the regulatory framework that enables products to reach patients. As part of a small Quality & Regulatory team, the successful candidate will take ownership of day-to-day quality and regulatory activities across the product lifecycle. The role spans both Regulatory Affairs and Quality Management, with responsibilities including supporting product development projects, maintaining technical documentation, handling interactions with Notified Bodies and authorities, overseeing post-market surveillance activities and ensuring compliance with applicable regulations and standards such as EU IVDR and ISO 13485. The position offers significant influence and visibility within the company. Working closely with Product Development, Product Management and Operations, the Quality and Regulatory Manager will act as a key business partner, helping shape regulatory strategy, support market access initiatives and ensure that quality and compliance considerations are integrated into decision-making. The position is based at our office in Uppsala. We work on-site at least three days per week and you will be part of a small Quality & Regulatory team, reporting to the Director of Operations, Quality & Regulatory. Duties & Responsibilities Represent Quality & Regulatory in new product development and product lifecycle management projects. Provide impact assessments for design, manufacturing, process and supplier changes. Prepare, review and maintain regulatory technical documentation, including documentation required under EU IVDR. Manage interactions with Notified Bodies and regulatory authorities, including submissions and change notifications. Participate in regulatory intelligence activities and monitor global regulatory requirements applicable to our products and operations. Review customer-facing materials, including data sheets, user manuals and website content, for accuracy and regulatory compliance. Represent the Quality & Regulatory function during internal and external audits. Contribute to market access activities supporting expansion into new markets, beginning with CE marking under EU IVDR. Conduct annual product dossier reviews and maintain post-market surveillance documentation. Support Quality Management System processes, including complaint handling, change control, CAPA, management review and audits. Drive the continuous improvement and effectiveness of the Quality Management System, ensuring compliance with ISO 13485 and applicable regulatory requirements. Your Profile The ideal candidate has several years of hands-on experience within the medical device or IVD industry, a practical understanding of quality and regulatory requirements, and the ability to translate regulations into workable solutions. Success in the role requires a proactive, self-driven and collaborative mindset, as well as the confidence to operate in a fast-moving scale-up environment where priorities evolve and individuals are expected to take ownership beyond their job description. Documented hands-on experience in medical device and/or IVD compliance management is a firm requirement for this role. Competencies & Areas of Expertise BSc degree or higher in life sciences, pharmacy, biomedical engineering, chemistry, or a related field. 5+ years of experience in a regulated medical device or IVD environment. Documented hands-on experience in regulatory affairs and/or quality management for medical devices or IVDs. Solid understanding of ISO 13485 and EU MDR/IVDR requirements. Professional proficiency in written and spoken English. It would be an advantage if you also have experience with: FDA regulatory requirements, including 21 CFR Part 820 and QMSR. Analytical reagent development and manufacturing. How to apply If this sounds like the right next step for you, submit your application. If you have questions about the role or the process, don't hesitate to reach out to Sandra Bydell Sveder at SallyQ ([email protected], 0763199688). About Rarity Bioscience Our superRCA® technology delivers unmatched sensitivity for detecting low-frequency mutations — enabling deeper insights into disease biology and earlier detection of relapse. A growing portfolio of superRCA kits is already in the hands of researchers and clinicians, with more on the way. We are about 30 people in Uppsala, working across functions without unnecessary layers. The culture is open, direct and prestige-free. Joining us means becoming part of a mission-driven team working to advance precision medicine through pioneering genetic analysis technologies, with the opportunity to make an impact on patients, healthcare and the future of molecular diagnostics.