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Roche

Global pharmaceuticals and diagnostics company

Expert Android Design System Engineer

Full-TimeUpdated on 10/23/2026
€3.8k/mo
Senior
Vienna, Austria+1 moreMore locations: Sant Cugat del Vallès, Barcelona, Spain
In PersonWork is located in either Vienna or Sant Cugat del Vallès.
Software EngineeringMobile Engineering

About the job

Requirements
  • Have at least 5 years of experience as an Android developer.
  • Have expert-level proficiency in Kotlin, Jetpack Compose, and Git.
  • Have experience with Material Design 3 for Jetpack Compose and design systems generally.
  • Have strong experience building reusable, testable, composable user-interface components.
  • Be proficient in writing unit tests, screenshot tests, and Jetpack Compose user-interface tests.
  • Have deep knowledge of accessibility best practices in Jetpack Compose.
  • Have knowledge of right-to-left (RTL) layouts.
Responsibilities
  • Architect, develop, and maintain mobile design-system components and interaction patterns consistent with platform strategies, governance policies, and standards.
  • Write and review clean, testable, scalable code aligned with best practices and design patterns.
  • Maintain code quality through automated testing, code reviews, and continuous-integration pipelines.
  • Provide technical assessments of mobile design-component development, ensuring quality, customer focus, forward thinking, and ease of use.
  • Participate actively in creating architecture for mobile applications consistent with platform strategies, governance policies, and standards.
  • Collaborate with design and development teams to align goals, scope, and business outcomes.
  • Document mobile components and support the mobile development community in their adoption, implementation, testing, and maintenance.
  • Work with project leaders, architects, designers, and front-end developers to understand client needs and resolve questions.
  • Champion design-system adoption with clients and usability engineers across Roche.
  • Brainstorm improvements and propose innovative solutions to improve community engagement.
  • Evaluate new technologies, patterns, and frameworks for potential adoption.
  • Contribute to design reviews, prototypes, and mobile user-experience standards.
  • Create documentation for AI agents so design-system users can build with the library using vibe coding.
  • Create test applications using vibe coding to verify the library’s compatibility with AI.
  • Document all components in Figma Code Connect.
Desired Qualifications
  • Have an interest in modern technology trends and best practices.
  • Have curiosity about areas outside Android development, including iOS development and cross-platform solutions.
  • Have experience with inner-sourced products.
  • Be engaged in developer communities, community management, and active contributions to open-source solutions.
  • Have experience creating third-party libraries.
  • Be familiar with Dokka and documentation deployment.
  • Be familiar with GitHub Actions.
  • Have knowledge of design or Figma tokens and their use in a custom design system.
  • Have experience working in a regulated environment.
  • Have knowledge of JavaScript or TypeScript.

About the company

Roche is a global leader in pharmaceuticals and diagnostics. It develops medicines and diagnostic tools that help detect, monitor, and treat diseases, using research and biotechnology to drive new therapies and tests. Roche combines drug development with in-house diagnostic products to support personalized medicine, where treatments are tailored to individual patients based on test results. Its approach differs from many peers by integrating drug discovery with diagnostic capabilities and by expanding its research through strategic acquisitions (like Genentech) to strengthen its biotechnology and R&D capabilities. The company’s goal is to improve patient outcomes and healthcare worldwide by delivering reliable medicines, accurate diagnostic tests, and data-driven care.

Company Size

1-10

Company Stage

IPO

Headquarters

Basel, Switzerland

Founded

1896

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Simplify's Take

What believers are saying

  • Enicepatide delivered 15.5% weight loss in September 2026 and 22.7% in June.
  • pTau217 can scale immediately through Roche's existing lab network and improve Alzheimer diagnostics.
  • Roche's June 2026 data and September 2026 filings signal multiple obesity shots on goal.

What critics are saying

  • Eli Lilly and Novo Nordisk dominate obesity pricing, distribution, and physician mindshare today.
  • Enicepatide remains Phase II-only; Roche starts late-stage glycemic and cardiovascular studies in 2027.
  • If enicepatide disappoints, Roche burns its $2.7 billion Carmot bet and loses obesity credibility.

What makes Roche unique

  • Roche combines pharma, diagnostics, and installed cobas labs across 4,500 U.S. instruments.
  • Elecsys pTau217 won FDA clearance on August 24, 2026, and CE marking September 7.
  • Roche controls obesity assets from Carmot and Zealand, spanning GLP-1/GIP and amylin.

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Benefits

  • Performance Bonus

Company News

Yahoo Finance
Oct 22nd, 2026
Roche reaffirms outlook as Q3 sales rise 7% to $19.6B, but growth doubts linger

Roche reaffirmed its 2025 outlook on Thursday and beat third-quarter sales expectations, but questions about its long-term growth remain. Group sales rose 7% to 16.1 billion Swiss francs (about $19.6 billion), ahead of the 15.8 billion franc consensus estimate. Jefferies analyst Michael Leuchten said a new resource planning system boosted revenue, making the results "cosmetically ahead." Roche still expects group sales growth in the "mid single digit range" and did not raise guidance. Sales of allergy and asthma drug Xolair reached only 848 million francs, well below estimates. A copycat version launched in the US this month, and Ocrevus and Tecentriq face generic competition by 2030. Roche is counting on its breast cancer pill giredestrant, which awaits a US Food and Drug Administration decision by December 18, and on obesity drugs. It says the products could together reach $9 billion in peak annual sales.

CNBC
Oct 22nd, 2026
Roche CEO presses Germany on growth strategy as drugmaker pauses investment there

Roche chief executive officer Thomas Schinecker has challenged Germany over its growth strategy, saying pharmaceutical firms are "the industry they need to bet on." Schinecker discussed the company's third-quarter earnings and its recent expansion in China. He also outlined recent pharmaceutical developments at the business. He explained why Roche has paused investment in Germany.

Yahoo Finance
Oct 16th, 2026
FDA approves Roche's Enspryng as first at-home injection for thyroid eye disease

Roche said the US Food and Drug Administration (FDA) has approved Enspryng (satralizumab) for adults with thyroid eye disease (TED). It is the first and only at-home subcutaneous treatment for the condition, and a patient or caregiver can administer it after training. In the Phase III SatraGO-2 trial, 52.9% of active TED patients on Enspryng had a proptosis (eye bulging) response, against 23.4% on placebo. Double vision fell in 60.7% of patients, against 25.8%. The SatraGO-1 trial missed its primary endpoint at Week 24. No new safety signals emerged. TED affects about 155 in every 100,000 people in the US. This is Enspryng's second approval, after neuromyelitis optica spectrum disorder in 2020. The FDA is also reviewing it for myelin oligodendrocyte glycoprotein antibody-associated disease, with a decision expected in January 2027.

Yahoo Finance
Oct 9th, 2026
FDA approves Roche's Tecentriq for stage III colon cancer, cutting recurrence risk by 50%

The US Food and Drug Administration has approved Roche's Tecentriq in combination with a fluoropyrimidine and oxaliplatin for adjuvant treatment of stage III deficient DNA mismatch repair colon cancer. This marks Tecentriq's twelfth approved indication in the US. The approval follows the phase III ATOMIC study, published in The New England Journal of Medicine, which demonstrated that Tecentriq plus chemotherapy reduced the risk of disease recurrence or death by 50% compared to chemotherapy alone. The 36-month disease-free survival rate was 86% with the combination versus 76% with chemotherapy alone. Nearly 25% of colon cancers are diagnosed at stage III, and almost one in three stage III patients experience recurrence within five years. This represents the first approved adjuvant immunotherapy regimen for this patient population. Roche is pursuing further regulatory filings, including with the European Medicines Agency.

Yahoo Finance
Sep 30th, 2026
Roche's enicepatide shows 22.5% weight loss in 48 weeks, challenging Eli Lilly and Novo Nordisk

Roche posted strong Phase 2 results for its weight loss drug enicepatide, showing 22.5% mean weight loss over 48 weeks. This compares favourably to Eli Lilly's Zepbound, which achieved 20.2% weight loss over 72 weeks in a separate trial. In another Phase 2 study, enicepatide demonstrated HbA1c reductions of up to 2.65 percentage points in diabetic patients after 48 weeks, compared to tirzepatide's 2.37 percentage points after 52 weeks. Despite promising results, Roche faces stiff competition from Novo Nordisk and Eli Lilly, which both have deep pipelines in development. Novo Nordisk's CagriSema is nearing approval, whilst Eli Lilly's retatrutide has posted strong Phase 3 results. Roche's revenue grew 6% year over year in the first half of the year to 30.4 billion Swiss francs.