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. 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. 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. 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. 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. 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.