Urwah Admin

Roche

As a pioneer in healthcare, Roche has been dedicated to improving lives since its founding in 1896 in Basel, Switzerland. The company develops innovative medicines and diagnostic tests that assist millions of patients worldwide. Roche combines advanced diagnostics and pharmaceuticals to tackle significant healthcare challenges, focusing on areas such as cancer, cardiovascular diseases, and neurological disorders. Guided by patient needs, Roche aims to prevent, stop, and cure diseases, ensuring healthier lives for individuals and communities.

Bei Roche kannst du ganz du selbst sein und wirst für deine einzigartigen Qualitäten geschätzt. Unsere Kultur fördert persönlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du für das, was du bist, wertgeschätzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl persönlich als auch beruflich wachsen kannst. Gemeinsam wollen wir Krankheiten vorbeugen, stoppen und heilen und sicherstellen, dass jeder Zugang zur Gesundheitsversorgung hat – heute und in Zukunft. Werde Teil von Roche, wo jede Stimme zählt.
 
Die Position
 
Step into a transformative role with us as an Disease Area Partner, where you will be at the heart of the evolving landscape of healthcare. Driven by groundbreaking innovation, greater patient empowerment, and the expanding wealth of medical information, our ecosystem is adapting to new challenges and heightened demands on public resources.
 As an Disease Area Partner, you will work locally, deeply integrated within the healthcare community, focusing exclusively on building meaningful stakeholder relationships without the constraints of sales targets or incentives. This allows you to focus entirely on delivering impactful, needs-based support for patients and healthcare providers.
 
Your Impact
 
<ul>
<li>Steward Roche’s products through their lifecycle and support their appropriate use, which includes sharing their merits with HCPs in a truthful and balanced manner</li>
<li>Implement campaigns with customers and distribute promotional materials as per marketing plan and customer needs</li>
<li>Organize group meetings in major hospitals</li>
<li>Propose new ideas related to campaigns, promotional material to the pod and are responsible for the implementation after approval.</li>
<li>Gathering Data& Insights from the market that would help the pod to make decisions.</li>
<li>The DA partner focuses on the importance of bringing the outside in, working with partners to uncover all potential opportunities to transform outcomes for patients, faster. They also bring the inside out, to bring Roche expertise, science and knowledge to the ecosystem.</li>
<li>Identifies important customers and keeps customer Personas up-to-date.</li>
<li>Continuously revises and updates the customer list& no. of patients in cooperation with the pod.</li>
<li>Positively participates in Internal meetings to review and discuss: achievements, Opportunities/challenges, Competitors activities.</li>
<li>Reporting Adverse Events to the Local Safety Unite within Roche timelines.</li>
<li>Ensuring great experiences whenever stakeholders in the ecosystem engage with Roche employees, products and services.</li>
</ul>
Who you are
 
<ul>
<li>You bring 1-2 years of experience within the pharmaceutical industry.</li>
<li>You have good business acumen, with desired experience in commercialization, medical, and customer experience excellence, and can leverage digital tools effectively</li>
<li>You demonstrate a personal commitment to improving the patient journey, with a strong drive to create value and impact on the ecosystem</li>
<li>You embody a strategic vision to enhance patient journeys and embed this within your actions</li>
<li>You possess an entrepreneurial mindset, continuously seeking opportunities to innovate and contribute</li>
<li>You maintain a growth mindset, learning and unlearning rapidly, experimenting, and sharing insights within and beyond Roche</li>
<li>You display integrity in every action, upholding honesty, ethics, and authenticity</li>
<li>You bring excellent stakeholder engagement skills, effectively partnering with therapeutic area experts (TAEs), organizations, and ideally with patient advocacy groups (PAGs)</li>
<li>You are fluent in the local language and proficient in English, facilitating collaboration across Roche’s broader enterprise.</li>
</ul>
Wer wir sind
 
Eine gesündere Zukunft treibt uns zur Innovation an. Mehr als 100.000 Mitarbeiter weltweit arbeiten gemeinsam daran, wissenschaftliche Fortschritte zu erzielen und sicherzustellen, dass jeder Zugang zur Gesundheitsversorgung hat – heute und für zukünftige Generationen. Durch unser Engagement werden über 26 Millionen Menschen mit unseren Medikamenten behandelt und mehr als 30 Milliarden Tests mit unseren Diagnostik-Produkten durchgeführt. Wir ermutigen uns gegenseitig, neue Möglichkeiten zu erkunden, Kreativität zu fördern und hohe Ziele zu setzen, um lebensverändernde Gesundheitslösungen zu liefern.
 
Gemeinsam können wir eine gesündere Zukunft gestalten.
 
Roche ist ein Arbeitgeber, der die Chancengleichheit fördert.

Disease Area Partner - Cairo

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
 
The Position
 
Roche is seeking a strategic and collaborativeERP Product Lifecycle Management Business Partner to join the Informatics ERP Team at Roche. In this role, you will partner closely with business stakeholders across Roche Diagnostics and Roche Diabetes Care to drive digital transformation initiatives spanning Enterprise Resource Planning (ERP) and Product Lifecycle Management (PLM) capabilities.
 The successful candidate will act as a trusted advisor between business functions and Informatics teams, ensuring that enterprise solutions align with operational, regulatory, product development, and manufacturing objectives across the Diagnostics discipline and Diabetes Care portfolio.
 
The Opportunity: 
This role requires strong cross-functional engagement, business process expertise, and the ability to translate complex business requirements into scalable technology solutions.
 
Business Partnership& Stakeholder Engagement
 
<ul>
<li>Serve as the primary Informatics business partner for ERP and PLM initiatives within Roche Diagnostics and Roche Diabetes Care.</li>
<li>Build strong relationships with stakeholders across R, Manufacturing, Supply Chain, Quality, Regulatory, Commercial, and Operations teams.</li>
<li>Facilitate alignment between business strategy and enterprise technology roadmaps.</li>
<li>Drive effective communication between business users, solution architects, vendors, and delivery teams.</li>
</ul>
ERP& PLM Strategy and Delivery
 
<ul>
<li>Lead and support ERP and PLM transformation initiatives across Diagnostics and Diabetes Care.</li>
<li>Identify opportunities for process optimization, harmonization, and digital innovation.</li>
<li>Translate business requirements into functional and technical solution designs.</li>
<li>Support implementation, enhancement, integration, and lifecycle management of ERP and PLM platforms.</li>
<li>Participate in global PLM initiatives and projects, ensuring consistency and scalability of solutions across Roche divisions.</li>
<li>Provide support for system testing, validation, and compliance in accordance with regulated industry standards (e.g., GxP).</li>
<li>Troubleshoot issues, provide end-user support, and contribute to continuous improvement efforts.</li>
<li>Collaborate with enterprise architecture and data governance teams to ensure scalable and compliant solutions.</li>
</ul>
Diagnostics& Diabetes Care Support
 
<ul>
<li>Partner with Roche Diagnostics business units to support product development, manufacturing, and quality processes.</li>
<li>Support Roche Diabetes Care initiatives involving connected devices, product traceability, regulatory compliance, and lifecycle management.</li>
<li>Ensure systems and processes support global healthcare and medical device regulations.</li>
</ul>
Governance& Compliance
 
<ul>
<li>Ensure ERP and PLM solutions comply with Roche quality standards, cybersecurity policies, and regulatory requirements.</li>
<li>Support validation activities and documentation in regulated environments.</li>
<li>Participate in governance boards, release planning, and portfolio prioritization activities.</li>
</ul>
Change Management& Continuous Improvement
 
<ul>
<li>Support organizational change management activities related to ERP and PLM adoption.</li>
<li>Develop and deliver stakeholder engagement and training strategies.</li>
<li>Drive continuous improvement through metrics, feedback, and operational excellence practices.</li>
</ul>
Who you are: 
Required Qualifications
 
<ul>
<li>Bachelor’s or Master’s degree in Information Technology, Computer Science, Engineering, Business Administration, or related discipline.</li>
<li>10+ years of experience in ERP, PLM, or enterprise systems business partnering roles.</li>
<li>Strong understanding of ERP platforms such as SAP S/4HANA and PLM ecosystems.</li>
<li>Understanding of SAP integration with modules like MM (Materials Management), PP/PI(Production Planning and Execution), PM (Plant Maintenance), QM (Quality Management), and SD (Sales& Distribution).</li>
<li>Experience supporting manufacturing, supply chain, product development, or quality processes.</li>
<li>Proven ability to work across global, matrixed organizations.</li>
<li>Strong analytical, communication, and stakeholder management skills.</li>
<li>Experience operating in regulated industries such as healthcare, medical devices, diagnostics, or pharmaceuticals.</li>
</ul>
Preferred Qualifications
 
<ul>
<li>Experience within Diagnostics, Medical Devices, or Diabetes Care environments.</li>
<li>Knowledge of product lifecycle management processes including design control, change management, BOM management, and product data governance.</li>
<li>Familiarity with Agile delivery methodologies and product-centric operating models.</li>
<li>Experience with system integrations between ERP, PLM, MES, QMS, and related enterprise platforms.</li>
<li>Understanding of GxP, FDA, ISO 13485, and other healthcare regulatory frameworks.</li>
</ul>
Desired Competencies
 
<ul>
<li>Strategic thinking and business acumen</li>
<li>Strong collaboration and influencing skills</li>
<li>Ability to navigate complex enterprise environments</li>
<li>Customer-focused mindset</li>
<li>Continuous improvement orientation</li>
<li>Strong leadership and facilitation capabilities</li>
</ul>
Relocation benefits are not available for this job posting.
 
The expected salary range for this position based on the primary location of Indianapolis is between $108,700 - $201,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
 Benefits
 
#RDT2026
 
Who we are
 
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
 
Let’s build a healthier future, together.
 
Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
 
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this formAccommodations for Applicants.

ERP Product Lifecycle Management Business Partner

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
 
The Position
 
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.
 
The Clinical Development Lead, Oncology/Pathology is responsible for planning and implementation of Clinical Development activities for novel medical value diagnostic solutions in the areas of oncology and tissue-based pathology at Roche Diagnostic Solutions (RDS), with a primary focus on Companion diagnostic/Personalized Healthcare solutions.
 
The Opportunity: 
<ul>
<li>Designs scientifically sound clinical studies and study programs in cross-functional teams</li>
<li>Makes substantial contributions to the Clinical Development strategy for the relevant therapeutic/disease area(s)</li>
<li>Leads clinical study design and execution, including critical review of study results, protocol and report generation to support new product development</li>
<li>Works with colleagues from Clinical Operations, Regulatory Affairs, Biometrics, Development, Quality, Business, and other functions to ensure appropriate implementation of clinical development strategies</li>
<li>Leads medical/scientific input and preparation of regulatory submissions as well as responses to reviewers from regulatory agencies</li>
<li>May participate in external interactions with health authorities (HAs)</li>
<li>Maintains clinical, regulatory, and scientific expertise as it relates to IVD product development and regulatory documentation</li>
<li>Builds and maintains close relationships with external thought leaders, supports preparation of advisory boards within the assigned indication area</li>
<li>Builds and maintains strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, in meeting business goals and ensuring operational excellence</li>
<li>Drives competitive differentiation, innovation and early pipeline activities and develops intellectual property strategy</li>
<li>Develops and manages external development partnerships (industry and academia)</li>
<li>Leads comprehensive literature reviews, supervises collation of relevant clinical and scientific information from different sources, and creates new scientific content (without guidance/direction)</li>
<li>Solves or leads others to solve complex outcomes; uses sophisticated analytical thought to</li>
<li>exercise judgment and identify innovative solutions</li>
<li>Acts as a coach for colleagues with less experience and helps them develop skills/expertise</li>
<li>Permanently optimizes processes to increase quality and efficiency standards</li>
<li>Drive patient and customer-centricity (mindset, behaviors and actions) by always putting the needs of patients and the customers first</li>
<li>Partner across diverse regions, cultures, and time zones to create an environment of belonging, inclusion and diversity</li>
<li>Working across Medical Affairs and Clinical Operations communities to identify mutual value and opportunities for collaboration</li>
<li>Demonstrate flexibility and adaptability to perform in a fast-paced, matrixed environment where fluid, cross-team collaboration is crucial</li>
<li>Model Roche’s values of integrity, courage, and passion (culture, mindset and behaviors)</li>
</ul>
Who You Are
 
<ul>
<li>You have a medical degree or advanced degree (PhD, PharmD or equivalent) in Life Sciences, Oncology, Immunology, Molecular Biology and or Anatomic Pathology</li>
<li>You have 7+ years academic, diagnostics or pharma industry experience,</li>
<li>You have familiarity with global regulatory bodies (FDA, EMA, PMDA)</li>
<li>You have good knowledge in applicable standards and regulations (ICH-GCP, IVDD/IVDR, MDR, FDA, NMPA regulations etc.) and understanding of the healthcare industry or equivalent academic experience</li>
<li>You have in-depth knowledge of the multidisciplinary functions involved in a company’s drug development process, e.g., clinical operations, biostatistics, regulatory, commercial, etc. and can proactively integrate multiple perspectives into the clinical development process and strategy for best end-results</li>
<li>You have the ability to work with pharmaceutical partners to align the development of a diagnostic test with the development of a specific cancer drug</li>
<li>You have the ability to travel required up to 10% (can vary per project phase and position)</li>
<li>You have the ability to work independently</li>
</ul>
The primary location for this position is Tucson, Arizona, USA (preferred). We will consider US remote candidates.
 
Relocation benefits aren't offered for this position
 
The expected salary range for this position is based on the primary location Tucson, AZ is 120,500-223,700. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance.
 
This position also qualifies for the benefits detailed at the link provided below.
 Benefits
 
Who we are
 
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
 
Let’s build a healthier future, together.
 
Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
 
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this formAccommodations for Applicants.

Clinical Development Lead, Oncology/Pathology

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
 
The Position
 
As Chapter Lead and Head of SBX Assays, you will drive the clinical translation of cutting-edge technology into RUO and regulated products that redefine the standard of care in precision oncology and genetics. You will provide strategic and technical leadership to define the next generation of oncology diagnostics—ranging from multi-cancer early detection to ultra-sensitive MRD monitoring.
 
You will lead the end-to-end evolution of novel clinical solutions, bridging the gap between novel workflow tools and high-throughput commercial implementation. Your leadership will ensure that our assays are not just innovative, but are robust, scalable, and clinically validated to meet the most stringent regulatory standards (PMA/IVD).
 
Key Responsibilities: 
<ul>
<li>Oncology Product Roadmap: Partner with Executive Leadership and Business teams to identify high-value clinical unmet needs and translate them into a multi-year technology roadmap.</li>
<li>Strategic Execution: Drive development of proprietary oncology assays, including defining performance requirements (LOD, sensitivity, specificity) that exceed current market standards.</li>
<li>Product Realization& Scale: Oversee the critical transition of assays from R into a CLIA/CAP or IVD-regulated environment, ensuring manufacturability and operational scalability.</li>
<li>Assay Innovation& De-risking: Implement and de-risk emerging technologies for use in clinical applications (e.g., epigenetics, fragmentomics, multi-omics).</li>
<li>Regulatory: Partner with Regulatory and Quality teams to design analytical and clinical validation studies (LoD, LoB, Precision) that meet FDA/PMA standards for Breakthrough Device designations.</li>
<li>Evidence Generation& KOL Engagement: Help define the clinical evidence strategies required for medical utility based on high-level scientific exchange with top-tier academic centers and biopharma partners.</li>
<li>Bioinformatics Integration: Architect the interface between wet-lab chemistry and Computational Biology to optimize "sample-to-variant" pipelines, focusing on digital error suppression and signal-to-noise optimization.</li>
<li>Operational Leadership: Drive 'Best-in-Class' technical standards across the organization, ensuring consistency in assay development methodologies and cross-functional alignment on technical KPIs.</li>
<li>Value Communication: Present scientific and clinical value propositions at webinars, workshops, or customer meetings.</li>
<li>Champion Our Culture: Foster a "Culture of Rigor" that balances rapid prototyping with the disciplined documentation required for regulated medical products.</li>
</ul>
Who You Are: 
(Required)
 
Education Level: 
<ul>
<li>Ph.D. or MD/PhD ​Molecular Biology, Oncology, Genetics, or related fields</li>
</ul>
Experience: 
<ul>
<li>10+ years in the molecular diagnostics industry.</li>
<li>Proven track record of launching one or more NGS-based clinical assays (IVD or high-complexity LDT).</li>
<li>Management experience of large multidisciplinary scientific teams for 7+ years</li>
</ul>
Knowledge, Skills, and Abilities: 
<ul>
<li>NGS Mastery: Deep expertise in library preparation (e.g., UMI tagging, hybrid capture) and their direct impact on clinical sensitivity and limit of detection (LOD).</li>
<li>Clinical Vision: Comprehensive understanding of the "Cancer Continuum," including solid tumor profiling, hematological malignancies, and the nuances of liquid biopsy.</li>
<li>Regulatory Experience: Proven track record of navigating the Design Control process (21 CFR 820) and launching at least one NGS-based clinical assay (IVD or high-complexity LDT).</li>
<li>Technical Diplomacy: Exceptional ability to navigate complex stakeholder environments and influence and guide senior functional experts who do not report to you directly.</li>
<li>Scientific Presence: A sustained record of innovation, evidenced by high-impact peer-reviewed publications or patents in ctDNA, methylation, or early detection.</li>
<li>Business acumen: Experience in portfolio prioritization and resource allocation within a matrixed R organization</li>
<li>Travel Requirements: ability to travel 15 - 20% of time to fulfill various business needs, including global oncology conferences and customer meetings</li>
</ul>
Preferred: 
<ul>
<li>You have demonstrated strong interpersonal and communication skills with the ability to communicate complex technical knowledge in a clear and understandable manner to a multidisciplinary team.</li>
<li>You have strong problem-solving skills with the ability to work independently</li>
<li>You have excellent written and verbal communication skills to effectively influence cross-functional stakeholders.</li>
</ul>
This is an on-site position based in Santa Clara, CA or Pleasanton, CA.
 Relocation benefits are not being offered for this role.
 
The expected salary range for this position based on the primary location of Santa Clara, CA is $195,300 - $362,750. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. We encourage all qualified applicants to apply. The role's level (& title) may be adjusted based on experience and qualifications.
 
A discretionary annual bonus may be available based on individual and Company performance.
 
This position also qualifies for the benefits detailed at the link provided below.
 Benefits
 
Who we are
 
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
 
Let’s build a healthier future, together.
 
Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
 
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this formAccommodations for Applicants.

Chapter Lead, Head of SBX Assays

<div>Bei Roche kannst du ganz du selbst sein und wirst f&uuml;r deine einzigartigen Qualit&auml;ten gesch&auml;tzt. Unsere Kultur f&ouml;rdert pers&ouml;nlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du f&uuml;r das, was du bist, wertgesch&auml;tzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl pers&ouml;nlich als auch beruflich wachsen kannst. Gemeinsam wollen wir Krankheiten vorbeugen, stoppen und heilen und sicherstellen, dass jeder Zugang zur Gesundheitsversorgung hat &ndash; heute und in Zukunft. Werde Teil von Roche, wo jede Stimme z&auml;hlt.<div></div><div>
Die Position</div><div>
We are looking for an Order Management and Distribution Specialist (Contractor) to join the Roche Diagnostics Turkiye team.</div><div></div>
Key Responsibilities:<ul><li>
Process domestic and international customer orders, schedule shipments according to the delivery calendar, and handle invoicing procedures.</li><li>
Ensure customers adhere to order timelines based on the planned schedule.</li><li>
Maintain continuous communication with customers throughout supply chain processes, acting proactively to address potential issues and taking necessary actions.</li><li>
Carry out shipment and return processes for devices in compliance with agreements.</li><li>
Collaborate with international teams to resolve potential system-related issues.</li><li>
Take an active role in driving continuous improvement within business processes.</li></ul>
Who You Are :<ul><li>
You are graduated from university departments such as Economics, Statistics, Econometrics, or Mathematics.</li><li>
You are fluent in English.</li><li>
You know about ERP programs (e.g., SAP, Netsis).</li><li>
You are experienced in import and export processes, preferably</li><li>
You are skilled in MS Office applications.</li><li>
You have strong interpersonal and communication skills.</li><li>
You are team-oriented, with the ability to take initiative.</li></ul><div> 
Wer wir sind</div>
Eine ges&uuml;ndere Zukunft treibt uns zur Innovation an. Mehr als 100.000 Mitarbeiter weltweit arbeiten gemeinsam daran, wissenschaftliche Fortschritte zu erzielen und sicherzustellen, dass jeder Zugang zur Gesundheitsversorgung hat &ndash; heute und f&uuml;r zuk&uuml;nftige Generationen. Durch unser Engagement werden &uuml;ber 26 Millionen Menschen mit unseren Medikamenten behandelt und mehr als 30 Milliarden Tests mit unseren Diagnostik-Produkten durchgef&uuml;hrt. Wir ermutigen uns gegenseitig, neue M&ouml;glichkeiten zu erkunden, Kreativit&auml;t zu f&ouml;rdern und hohe Ziele zu setzen, um lebensver&auml;ndernde Gesundheitsl&ouml;sungen zu liefern.
Gemeinsam k&ouml;nnen wir eine ges&uuml;ndere Zukunft gestalten.
Roche ist ein Arbeitgeber, der die Chancengleichheit f&ouml;rdert.</div>

Order Management & Distribution Specialist (Contractor)