H3About Us /h3pa Ikerian AG (formerly RetinAI Medical) /a is a fast-growing medical device software company headquartered in Bern, Switzerland. Our mission is to enable the right decisions sooner in healthcare, through transformative AI data management solutions for disease screening and monitoring. Join our diverse team of entrepreneurs, developers, researchers, and commercial experts who are collectively shaping the future of healthcare. /ph3Job Description /h3pWe are looking for a strongHead of Quality Regulatory Affairs (QRA) /strong to join our company in Bern, Switzerland. This role is pivotal in driving our internal operational maturity and ensuring global compliance across our expanding product portfolio. Following Ikerian’s acquisition by EssilorLuxottica, you will lead the evolution of the QRA department from a high-growth startup environment to a world-class subsidiary operation. You will oversee global product clearances for Software as a Medical Device (SaMD), optimize our Quality Management System (QMS), and serve as a strategic partner to internal RD, Research, and global sister companies like Heidelberg Engineering. brKey Responsibilities /pulliLead and mentor a global QRA team located across various time zones, establishing a supportive, high-performance team culture driven by clear accountability, structured goal-setting, and skills development. /liliAct as the legal Person Responsible for Regulatory Compliance (PRRC) under EU MDR to ensure device conformity, keep technical documentation up to date, and oversee post-market surveillance and vigilance reporting obligations. /liliDevelop and execute robust global regulatory strategies with an emphasis on securing and maintaining rapid market access via FDA submissions and CE-MDR compliance frameworks. /liliGovern and scale a world-class Quality Management System (QMS) ensuring continuous organizational readiness for ISO 13485 and the Medical Device Single Audit Program (MDSAP). /liliServe as the primary corporate representative during all internal, Notified Body, partner, and health authority audits to ensure the continuous validation of corporate certifications. /liliEstablish structured cross-functional alignment with RD to seamlessly integrate design controls, risk management, and software lifecycles into early product development stages. /liliPartner with the IT Infrastructure and Security functions to support data privacy governance frameworks including GDPR and HIPAA compliance while aligning quality processes with emerging cybersecurity standards. /liliTranslate market intelligence and evolving global regulations into proactive compliance roadmaps to ensure customer specifications and changing health authority standards are built into the corporate lifecycle. /li /ul pstrongRequirements /strong /pulliUniversity degree in Life Sciences, Biomedical Engineering, Law, or a relevant scientific discipline; a PhD or MBA is a strong asset. /liliA minimum of 10 years of professional experience with a documented track record of successfully leading, managing, and mentoring cross-functional quality and regulatory teams. /liliA minimum of 8-10 years of dedicated industry experience in medical device Quality and Regulatory Affairs specifically focused on Software as a Medical Device (SaMD). /liliProven track record as a legal Person Responsible for Regulatory Compliance (PRRC) with deep experience managing complex technical files for EU MDR and FDA submissions. /liliExpert technical knowledge of ISO 13485, EU MDR, IEC 62304 software lifecycles, ISO 14971 risk management, and FDA 21 CFR Part 820. Formal Lead Auditor certification is highly valued. /liliDemonstrated ability to manage multi-faceted projects involving complex technical, clinical data, and regulatory evaluation components across international borders. /liliExcellent verbal and written English communication skills. /liliStrong analytical and problem-solving abilities with an exceptional eye for process detail, operational efficiency, and structural quality. /liliDemonstrated entrepreneurial and collaborative mindset with excellent team-building and conflict-resolution capabilities. /liliAbility to work independently as a leader. /liliAvailable to work during Central European Time (CET) business hours with a regular physical presence at our Bern headquarters. /li /ul pstrongBenefits /strong /ppWhat We Offer /pulliA chance to be part of an exceptional global team driving innovation in healthcare. /liliA competitive salary in a supportive work environment that fosters work-life balance. /liliOpportunities for professional growth and development in an international setting. /liliA culture of collaboration and inclusion, which is fundamental to our ethos. /liliOccasional travel to our HQ in Switzerland, immersing you in our core operations and company culture. /li /ul