Are you a senior designer who thinks in workflows and mental models — and wants to shape how a complex clinical platform evolves across genomics, oncology, imaging, and real‑world data? Join our Platform Design & Innovation team to own cross‑cutting design problems across SOPHiA DDM™: a multimodal platform serving geneticists, pathologists, oncologists, bioinformaticians, and pharma researchers in one of the most consequential domains in healthcare.
You’ll design for expert users operating under clinical pressure — not for consumer simplicity — and your work will directly influence what gets built across variant interpretation, oncology decision support, radiomics, and research data access. This is a role where design changes outcomes, and where the complexity is the point.
As a designer who earns trust with engineers and PMs, moves fast from research to prototype to validation, and wants a clear path toward leading a design function, we invite you to join the SOPHiA GENETICS Platform Design & Innovation team as our new Senior Platform Designer. This is a senior individual‑contributor role with a clear path to team leadership.
This is a hybrid opportunity, requiring 3 days onsite at our corporate office in Rolle, CH.
Your Mission
As our Senior Platform Product Designer, you will combine genuine product design depth with rapid prototyping capability and the product judgment to drive design decisions from user research through to shipped features.
Own cross‑platform design problems
* Lead the design of major DDM platform workflows across the full product surface: variant triage and interpretation in the genomics platform, oncology decision‑support workflows in Carepath, multimodal data views that combine genomic and imaging signals, and DataHub experiences for clinical and pharma research users.
* Define and evolve the cross‑surface interaction patterns that give the platform coherence: how data from different modalities is presented together, how classification decisions are recorded and traced, how clinical and research users with different expertise levels navigate the same underlying data.
* Govern and evolve the DDM design system in collaboration with engineering: component usage, token standards, interaction primitives, and the documentation that makes the system usable across teams.
Work at expert‑user depth – across diverse user groups
* Conduct research with users across the platform’s range: genomics experts operating at high information density (geneticists, pathologists, bioinformaticians), oncologists and clinicians using Carepath for treatment decision support, and pharma researchers accessing real‑world data through DataHub. These are not the same user; designing well for each without fragmenting the platform is the hard problem.
* Design for appropriate complexity — not for consumer simplicity. Expert users read variant tables and imaging reports under clinical pressure; pharma researchers need research‑grade data access with audit controls; oncologists need actionable summaries without losing access to underlying evidence. Your designs must match the cognitive model of whoever is in front of the screen.
* Balance clinical workflow fidelity with IVD regulatory constraints: traceability, audit trail, accessibility, and the interaction patterns that survive regulatory review.
Prototype and validate
* Build interactive prototypes to compress the time between concept and clinical feedback. Use whatever tooling compresses that cycle — AI‑assisted code, low‑code scaffolding, or hand‑crafted HTML — with the goal of getting something real in front of users quickly.
* Run validation sessions with clinical users, oncologists, and pharma partners early and continuously. Treat user research as a design input, not a sign‑off step.
Partner with engineering, product, and cross‑team stakeholders
* Work alongside platform engineering as a peer. Translate between the language of design (workflows, mental models, jobs‑to‑be‑done) and the language of engineering (APIs, data models, performance, security). The role succeeds when both teams move faster because of how well you operate at that boundary.
* Collaborate with Product Owners and Product Managers across application teams — HemOnc, Solid Tumor & LBx, RID, Carepath, DataHub. PDI’s mandate is transversal: you do not sit within one team’s scope, you influence platform‑level decisions across all of them. That requires earning trust with POs and PMs who have their own roadmaps and priorities, and shaping shared vision without direct authority.
* Contribute to requirements authoring — writing stories and acceptance criteria with enough precision that engineering can build from them.
* Maintain design system integrity across teams: component adoption, token consistency, and the documentation that makes the system adoptable.
Grow towards team leadership
* Build influence across engineering, product, data science, clinical stakeholders, and executive leadership. Raise the quality bar for design artifacts across teams. Develop readiness for team leadership: mentoring junior designers, shaping team process, and taking ownership of a design function.
Requirements – Experience & Craft
* A track record as a senior product or platform designer in environments where users are domain experts — clinical, scientific, or technical SaaS where workflows are genuinely complex and simplification is not the answer.
* A portfolio of shipped work showing product judgment: hard tradeoffs, designs evolved through validation, and clear evidence that your involvement changed what got built.
* Experience designing for multiple, distinct user groups within a single platform — and keeping the product coherent across them.
* Experience designing information‑dense, data‑heavy interfaces: tables, filters, multi‑step clinical or scientific workflows, multimodal data views.
* Experience in regulated environments (HealthTech, MedTech, scientific software) is a strong advantage. You understand that IVD design is held to a different standard and welcome that constraint.
Product and Technical Fluency
* Strong design system thinking: you understand that platform design produces leverage when its patterns are adopted across teams, and you can balance system coherence with the freedom that innovation work requires.
* Comfortable working close to code and close to product: you can author requirements and acceptance criteria, hold a meaningful conversation with engineers about implementation constraints, and build prototypes that go beyond static mockups.
* Rapid prototyping fluency — including with modern AI‑assisted tooling — used in service of faster clinical validation, not as an end in itself.
* Familiar with the engineering vocabulary of data‑intensive platforms: APIs, data models, performance, security, accessibility.
Domain and Leadership
* Genuine curiosity about the domain — clinical genomics, imaging, and real‑world data are technically rich and humanly consequential. The best designers in this space find the complexity more interesting, not more intimidating.
* Grounded understanding of AI/ML in a clinical context: not as a design aesthetic or a platform identity, but as a specific capability with regulatory, traceability, and expert‑trust requirements. Experience extending AI/ML features within a regulated product — where what you show, and how you show confidence, has clinical consequences — is a meaningful advantage.
* Excellent communicator and influencer across audiences — genomics experts, oncologists, pharma partners, engineers, Product Owners, executives. You can tell the story of a design decision in the language of whoever is in the room, and you can earn alignment with POs and PMs who did not ask for your input.
* Comfortable with ambiguity. You bring conviction without rigidity, and you adjust when research tells you something you didn’t expect.
* Readiness to grow into team leadership. You want to develop other designers and take ownership of a design function, not just your own work.
Benefits
* Sickness and Accident coverage through Helsana
* Meal vouchers at 90 CHF per month with our partner cafeteria
* A fun and engaging work environment, with rest & entertainment space, full stocked free coffee machine and free fruit/snacks
* Free parking in an easy to access location
* A strong social committee whose purpose is to make SOPHiA GENETICS both enjoyable as well as rewarding
* As our global HQ, you’ll have direct interaction and exposure to senior leadership and our executive team locally
Starting Date: ASAP
Location: Rolle, CH
Contract: Permanent
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