Hoffmann-LA Roche Inc jobs in Santa Clara, CA - 68 jobs

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 2026 Summer Intern - Computational Sciences and Informatics (CSI), Reagent Bioinformatics We advance science so that we all have more time with the people we love. Department Summary Reagent Bioinformatics, a sub-unit of CSI, supports diverse Roche RnD efforts for Library prep, Target Enrichment and Sequencing Solutions, for products both on-market and under development. This internship position is located in Pleasanton, on-site. The Opportunity * Develop, optimize NGS analysis pipelines and pipeline tools. * Provide recommendations based on benchmarking vs existing pipelines/tools. * Deployment of developed pipeline(s)/tools. * NGS analysis, summary, plotting, cross-run comparison. * Present results to key stakeholders to guide assay / RnD development. Program Highlights * Intensive 12-weeks, full-time (40 hours per week) paid internship. * Program start dates are in May/June 2026. * A stipend, based on location, will be provided to help alleviate costs associated with the internship. * Ownership of challenging and impactful business-critical projects. * Work with some of the most talented people in the biotechnology industry. Who You Are Required Education: You meet one of the following criteria: * Must be pursuing a PhD (enrolled student). Required Majors: Bioinformatics, Computational Biology, Molecular Biology, Computer Science or other quantitative field. Required Skills: * 2+ years of experience of NGS analysis: read QC, trimming, alignment, variant calling. * 1+ years of NGS pipeline or pipeline tool development * Proficiency in Python * Experience with Workflow management systems: Snakemake or Nextflow * Proficiency with data plotting and summarization Preferred Knowledge, Skills, and Qualifications * Excellent communication, collaboration, and interpersonal skills. * Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion. * You have experience with human genomics and / or infectious disease. * You are proficient with plotting and summarizing results with Jupyer Notebook. * You have experience in using singularity Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of California is $50.00 hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off 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 form Accommodations for Applicants.

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** Are you passionate about ensuring workplace safety, health, and environmental excellence? We are looking for a motivated and collaborative individual to join our team as a SHE Business Partner. In this versatile role, you will support diverse functional areas within the organization, helping to implement and maintain SHE policies and programs, while addressing unique challenges across manufacturing, R&D, facilities, and supply chain. With opportunities to lead key programs, contribute to cross-functional initiatives, and collaborate on impactful projects, this position offers an exciting chance to develop your expertise, make meaningful contributions, and help create a safer, more sustainable future for our team and beyond. Functions as a Safety, Health & Environmental (SHE) Business Partner for assigned functional areas (e.g. Manufacturing, Facilities, R&D, Supply Chain, etc.). In addition, will fulfill site-wide responsibilities for specific program area ownership. Expected to work on projects across the business functions, business units, and our business area. Applies knowledge and skills to complete a wide range of difficult tasks. Acts independently to determine methods and procedures on new assignments. Consults with management in the understanding of policies, procedures, programs, and company directives to ensure compliance. Duties are diverse and complex often involving research, analysis and solution development. Possesses and applies a comprehensive knowledge of a particular field across multiple business functions. Plans, conducts and oversees work involving large and important/complex projects. Reviews progress with management. Serves as a recognized resource to multiple Roche sites, corporate management, and/ or cross functional teams. May serve as a resource to all levels of personnel across our business area, including other Roche locations and assist external customers as needed. Works with independence to provide direction and guidance on issues to department leadership, business functions, and/or SHE staff members. **The Opportunity** **Job Duties/Responsibilities:** + Coordinates, develops, implements, and maintains SHE policies, procedures, and programs for regulatory programs, company-specific Directives and Standards, Bay Area-wide goals, and other company initiatives and requirements within assigned areas of responsibility under the direct supervision of a SHE Manager. + Executes tasks in support of SHE programs with direction and guidance from their manager. SHE program management responsibilities may include (but not limited to): Ergonomics (lab and office), Safety Signage, Site Inspections, Personal Protective Equipment, Seismic Safety, Event Safety, and Solitary Worker. + May serve as the subject matter expert in the implementation of one or more program areas. Leads the identification of program gaps and implementation of improvements with guidance and support of a SHE Manager. + Coordinates with assigned business functions, units, and/or our business area in order to help management establish objectives and ensure SHE compliance in health related SHE programs. + Supports basic, daily SHE business unit needs across multiple programs, under the direction of their manager, including: responding to SHE inquiries, facilitating and assigning SHE training, participating in department meetings and assisting with follow up on incident and inspection CAPAs. + Develops, implements, and conducts formal campus wide SHE inspections and audits. Assist with or lead external audits as required. Tracks resolution of issues. + Participates in emergency planning and emergency teams. Responds to emergency situations as needed. + Supports SHE management with projects or activities as assigned, which have impact across Molecular Solutions, Roche Divisional, and/or Corporate functions. + Other duties as assigned by management. **Competencies Identified for Success:** + Works well in a fast-paced environment with significant oversight and direction from their supervisor. + Effective communicator in both verbal (meeting leading, presentation, and training). and written formats (business e-mail, technical documents, programs). + Responsive to stakeholder inquiries and requests with a high sense of urgency. + Demonstrates the ability to stay organized, keep track of assignments and prioritize workload. + Highly effective team player and collaborator. Comfortable working in a matrix environment and leveraging expertise across functions. This may include participating in cross functional teams focused on creating value for the business. **Who You Are** Qualifications: Education, Experience, Knowledge and Skills _(Minimum requirements)_ + Education: BA, BS + 0-2 years of relevant experience with a BA/BS, preferably in pharmaceutical, biotech, medical device or high tech industries. Familiar with MicroSoft Word, Excel, and Powerpoint as well as the Google suite of programs (gMail, gCal, docs, sheets, slides, etc.) This position is not eligible for relocation. The expected salary range for this position based on the primary location of California is $67,600 - $125,600 USD Annual. 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 form Accommodations for Applicants (***************************************************************************************************** .

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** Global Access is focused on delivering sustainable, replicable, and scalable global strategies, policies, and solutions. Our work aims to support the Roche Pharma Vision and One Pharma Strategy and enables affiliates to drive patient access locally while maximizing the value for society, ecosystems, and business. We are operating in a highly networked and agile model with stable chapters and a variety of flexible squads and work product teams, operating across disease areas, functions, and geographies. The therapeutic areas of focus for this Position are CVRM and Oncology. As one of the Access Strategy Leads (ASLs), you play a critical role in ensuring Roche and healthcare systems deliver rapid, broad, and sustainable patient access to innovative offerings. The ASL acts as a strategic thought partner and expert, collaborating with cross-functional teams to develop and implement effective access strategies to ensure our commercialization and development strategies fully reflect market conditions and access considerations. The ASL drives the strategic integration of access by ensuring that Global Access (GA) expertise, and access and policy considerations are effectively incorporated into development and commercialization strategies at all phases of the lifecycle, including asset strategies, disease area strategies, and commercialization strategies. **The Opportunity** + Serve as the Primary Point of Contact (PPOC) for the unified Access team, championing the Access/Payers perspective on the Commercial Leadership Teams and ensuring their needs and challenges are prioritized. + Lead the development and implementation of holistic access strategies that are scalable, feasible, and balance patient access with sustainable pricing and reimbursement across markets. + Assemble, synthesize, and distill access insights from research, affiliate feedback, and GA intelligence into a compelling Disease Area (DA) Access strategic brief to shape and refine the commercialization strategy. + Ensure that the commercialization strategy seamlessly embeds access insights and deliverables by the unified Access team, and support the adoption of the access strategy in key markets by guiding local execution (providing Access Amplifier guidance and Objection handler support). + Ensure alignment with Access partners so that registrational trials and other clinical and non-clinical evidence packages are supportive of the overall access strategy, including the Integrated Evidence Package (IEP). + Co-create access materials and outputs that incorporate diverse stakeholder perspectives (such as HTA bodies, Payers, Policy Makers, Governments, Patients, Caregivers, and Society) to successfully support reimbursement submission and Access processes globally, and actively engage externally (e.g., Medical/Commercial Ad Board, Congresses). + Develop access assessments to inform investment decisions, valuations, and asset strategies for pipeline products and business development opportunities, and empower and coach GA partners to deliver key insights for integrated access assessments, strategies, plans, and their implementation. **Who You Are** + A Bachelor's Degree (life sciences, health economics, marketing, or medical), MBA, or other relevant Graduate or Postgraduate Degrees is required. + Significant pharmaceutical customer-facing experience, preferably in both global and country-level positions, or experience working within a cross-functional or integrated commercial team globally and locally. + You must have 8+ years of access experience in the pharmaceutical or related industry, with multidisciplinary experience within and beyond Access being an advantage. + The ability to work in a matrix organization, lead diverse teams to achieve common goals, and demonstrate strong knowledge of the drug development and commercialization process, as well as the current and future external environment. + The capability to understand complex scientific issues, translate them into effective access and business strategies, operate in ambiguity, and deliver impactful messages/strategic recommendations to a broad range of stakeholders, with deep knowledge of the Access landscape (e.g., US, China, EU4, UK, Canada). Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity! Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Basel. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. **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.**

Advances in AI, data, and computational sciences are transforming drug discovery and development. Roche's Research and Early Development organisations at Genentech (gRED) and Pharma (pRED) have demonstrated how these technologies accelerate R&D, leveraging data and novel computational models to drive impact. Seamless data sharing and access to models across gRED and pRED are essential to maximising these opportunities. The new Computational Sciences Center of Excellence (CoE) is a strategic, unified group whose goal is to harness this transformative power of data and Artificial Intelligence (AI) to assist our scientists in both pRED and gRED to deliver more innovative and transformative medicines for patients worldwide. The Opportunity: As a strategic leader within Roche's Computational Center of Excellence (CoE), the Chief of Staff plays a critical role in shaping and driving the CoE's vision, ensuring seamless execution of business strategy, and fostering cross-organizational collaboration. Reporting directly to the Head of CoE, this role acts as a key advisor and execution partner, enabling leadership effectiveness, driving strategic alignment across gRED and pRED, and enhancing the impact of computational sciences, data, analytics, and AI in drug discovery and development. Strategic Partner Act as a thought partner and trusted advisor to the Head of CoE on business, organizational, and operational strategies. Organize and prioritize critical issues and required information for the Head of CoE to facilitate efficient decision-making. Partner with the Head of CoE and CoE LT in strategic planning, policy development, and decision-making. Manage SVP priorities and communications, ensuring efficient use of time and resources in advancing computational drug discovery goals Serve as a spokesperson and advocate for the Head of CoE and their leadership team for internal and external global stakeholders at executive levels and across affiliates. Drive cross-functional alignment across research, development, and computational teams in a timeline manner to ensure effective implementation of data science and machine learning initiatives Lead special projects supporting SVP decision-making that require inputs from multiple research and computational disciplines Identify potential risks and opportunities in computational drug discovery initiatives, propose mitigation strategies, and monitor progress against key performance indicators CoE Leadership Team (CoE LT) Management Manage CoE LT meetings, including preparing agendas, ensuring materials are sent in advance, time is well spent, and objectives are achieved. Provide guidance on meeting agendas for broader leadership meetings led by the Head of CoE. Lead and/or facilitate productive debates on key business planning and organizationally relevant topics Ensure the SVP is well-prepared for internal and external meetings, including board meetings, scientific conferences, and partnership discussions Develop and execute internal communication strategies that align computational sciences initiatives with broader Genentech drug discovery objectives Maintain accurate confidential files and data records. Lead the planning of CoE LT offsites and events. Stakeholder Engagement and Cross-Functional Leadership: Build and maintain relationships with key stakeholders across research, development, clinical, and external partnerships in the computational sciences ecosystem Facilitate communication and collaboration between computational sciences teams and other drug discovery functions, ensuring alignment on critical decisions Work with leadership in cascading computational sciences goals across the organization and ensuring alignment with overall drug discovery objectives Track and manage computational sciences projects delegated across the company to ensure timely completion and strategic alignment Build a strong network with other Chiefs of Staff across Genentech and Roche to facilitate execution of computational sciences initiatives Foster a culture of collaboration, innovation, and continuous learning across computational sciences teams Key Success Factors: Build and maintain strong relationships with the Head of CoE, leadership team, and others in the organization to advise and influence outcomes. Assist and communicate with executives in decision-making, program management, and initiative implementation. Understand long term strategic, big-picture priorities while managing the detailed execution of deliverables. Navigate ambiguous situations to unearth and address core issues or challenges. Independently lead and drive cross-functional initiatives, projects, or programs at a leadership level. Develop new approaches to address complex organizational challenges that impact CoE and beyond. Facilitate resolution of issues relating to projects, priorities, and team dynamics. Demonstrate creativity, independence, neutrality, and initiative in resolving issues. Who you are: Advanced degree in computational sciences, data science, AI, biology, chemistry or a related field or equivalent experience desired. 10+ years in computational sciences, AI, data analytics, drug development, or life sciences industry. Proven ability to effectively partner with executive leaders in scientific/technical organizations. Highly skilled in strategic thinking, planning, and execution. Excellent written and verbal executive communication skills. Exceptional influencing skills and a consistent track record of driving strategic opportunities and problem-solving. Strong facilitation and problem-solving abilities, with a capacity to manage ambiguity. Experience in leading organizations and people through significant change and prioritization. Proven track record in all elements of people leadership-attraction, hiring, onboarding, development planning, performance management, coaching, and strategic talent evolution. Strong ability to communicate and influence across global, regional, and local cultures and business units. Ability to retain focus on long-term goals while addressing high-switching frequency for short-term actions. Knowledge of Genentech or Roche culture, systems, and organization is a plus. Travel Requirement: This role requires up to 30-35% travel for meetings, conferences, and strategic engagements. Relocation benefits are available for this job posting. The expected salary range for this position based on the primary location of California is $201,300-$373,800. 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 #ComputationCoE Genentech 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 form Accommodations for Applicants.

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** Acts as a link between global and local Finance, Supply Chain and Manufacturing, IT and Business Process Management and the project Aspire work streams to reach alignment within and across the divisions with specific focus on Roche Diagnostics. Translates detailed business requirements to IT organization and manages changes to such specifications. Defines and implements global template solutions including solution documentation & implementation, test management, business process operations including integrated training for the area of Supply Chain Finance. _Disclosure note: The opportunity is available on a fixed-term basis until the end of 2027._ **_The Opportunity_** + **Lead Process Design and Strategy:** Actively pursue and drive the implementation of the End-to-End Business Process Management (E2E BPM) strategy, defining global, cross-divisional, state-of-the-art process designs. + **Empowered Decision-Making:** Serve as an empowered decision-maker for your process area across divisions, operating within the E2E Business Process Management guardrails. + **Cross-Functional Alignment & Stakeholder Management:** Act as a critical link and strive for cross-functional and divisional alignment across Finance, Supply Chain, Operations, Procurement, IT, and Business Process Management to achieve E2E Process Harmonization. + **Lean and Standardized Solutions:** Design and implement lean cross-divisional processes and solutions, maximizing standardization and harmonization while collaborating closely with the E2E Global Business Process Managers (GBPMs). + **Template Support and Safeguarding:** Support and safeguard the Global ASPIRE Template and deployment activities, ensuring business acceptance globally. + **Solution Documentation & Implementation:** Define and implement global template solutions, including solution documentation, implementation via Standard Operating Procedures (SOPs), and integrated training for Supply Chain Finance. + **IT Liaison and Requirements Management:** Translate detailed business requirements for the IT organization and manage changes, leveraging strong IT knowledge to assess technical feasibility. + **Independent Task Execution:** Work independently to drive key tasks in the Supply Chain Finance stream, leveraging strong business knowledge to discuss, assess, and justify business requirements. **_Who you are_** We are looking for someone who is self motivated, really passionate about his or her job and understands that providing a high-quality service is crucial for the organization. As an ideal team member you are open-minded, dedicated to make a difference and open to constant development. Furthermore, you have: + Extensive Experience in Supply Chain Finance: Possess a Master's degree (or equivalent) and a minimum of 10 years of experience in Supply Chain Finance, management accounting, and product costing. + Global Transformation Leadership: Demonstrated ability to successfully lead major global transformational projects with a proven track record of cross-functional and cross-divisional implementation. + SAP & Process Expertise: Strong knowledge of SAP FI/CO, MM, PP, and MES systems, along with experience in driving SAP Supply Chain Finance process transformation and End-to-End process standardization. + Advanced Project & Business Skills: Expertise in Project Management, Business Process Management, superior analytical and problem-solving skills, and experience with agile, Lean, and rapid development methodologies. + Stakeholder & Communication Proficiency: Strong influencing skills and the ability to work effectively in complex global networks and with international teams, complemented by exceptional written and verbal communication skills in English. **_In exchange we provide you with_** + Development opportunities: Roche is rich in learning resources. We provide constant development opportunities, free language courses & training, the possibility of international assignments, internal position changes and the chance to shape your own career. + Excellent benefits: Competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party. + Flexibility: We also support flexibility to help you find your balance. Home office is commonly available (typically 2 office days/week on average). We create the opportunity for freedom in working, where your corporate and private life coexist in harmony. + A global inclusive community, where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion. _Please read the Data Privacy Notice for further information about how we handle your personal data related to the recruitment process:_ *********************************************************** **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.**

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** The GCS Mol Labs Senior Specialist - Application is the third in the series of four jobs. The employee is involved in defining the work scope and works autonomously with little to no supervisor direction. Serves as a technical expert on the product(s) and works on complex projects requiring broad knowledge of products and systems. **The Opportunity:** **Key Responsibilities** + Provides primary application support to the Development team, prioritizing the launch and support of new assays. + Provides application support to prospective partners for new assay development, demonstrating a strong understanding of customer workflows and portfolio direction. + Provides on-market support by addressing complex Level 2 application submissions independently with little or no direction. + Creates / revises curriculum for training sessions for internal staff and customers on new assays and workflows. + Delivers training to small and larger groups at Roche and Regional Support Centers. + Creates, updates, and reviews customer-facing documentation, including writing technical Application Notes. + Participates in and leads design review teams to provide service and application perspective, reviews and approves design change content, and creates the required deliverables. + Creates service requirements on development projects and advocates for functional goals. + Follows established Roche Quality System procedures in execution of work and identifies need for and creates new departmental procedures. + Other duties as assigned by management. **Who you are:** **Required Qualifications & Experience** Formal Training/Education: + **Formal Training/Education:** Bachelor's degree or higher (cellular biology, molecular biology, biochemistry or related field) and 5 years of relevant technical support experience (customer-facing role and incorporating experience with troubleshooting and training) AND Advanced knowledge of Next-Generation Sequencing. + Demonstrated theoretical and practical knowledge of Next-Generation Sequencing sample preparation workflows and applications, including experience with Molecular Biology/Biochemistry concepts, practices and procedures. Knowledge, Skills, and Abilities: + Proven ability to understand complex customer workflows and quickly learn new portfolio directions. + Possesses good communication, organizational, logical thinking, and presentation skills. Communicates complex and unfamiliar ideas and solutions easily to users with little or no technical knowledge. + Ability to work independently on assigned tasks of broad scope with minimal guidance or supervision. + Ability to interact with appropriate internal cross-functional groups, areas, and regions. + Courteous and customer-oriented. Works to satisfy internal and external partners. **Preferred Qualifications** + Experience with Sequencing (Seq) instruments and a background working closely with Development (Dev) teams is highly appreciated. + Knowledge of bioinformatics and NGS data analysis. + Strong written and oral communication skills, especially for writing technical documentation. + Previous experience mentoring and/or training. + Project management experience. **Travel Requirements/Location Requirements** + **Location:** Santa Clara, CA + **Travel time:** 25% both domestic and international, required. + **This position does not offer relocation.** The expected salary range for this position based on the primary location of California is $89,500 - $166,300.00. 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 form Accommodations for Applicants (***************************************************************************************************** .

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** **Molecular Clinical Specialist - Pacific Northwest Region** 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. Roche Molecular Diagnostics provides integrated, high-performance analytical systems to optimize laboratory management from pre-analytical to post-analytical processes. We develop high quality solutions for diagnostics laboratories - from analyzers and test reagents to work-flow solutions. To maintain its leadership in technology and quality, Roche minimizes third party products with more than 75 percent of its assay portfolio developed and manufactured in-house. **The Opportunity:** As a Molecular Clinical Specialist (MCS), you will play a key role in driving the success of Roche Molecular Diagnostics solutions. You will lead strategic sales efforts by engaging with healthcare professionals and laboratory leaders to convey the clinical and operational value of our molecular testing portfolio. In this role, you will: + serve as a key scientific and clinical resource, helping customers make informed decisions by simplifying complex technical information. + lead sales generation for assigned accounts or territories, focusing on large, complex, and high-visibility strategic accounts. + engage with customers, including visiting existing and prospective clients, expanding accounts, and acquiring new business. + partner with customers to understand their laboratory workflows, testing needs, and clinical priorities to deliver tailored solutions that improve patient outcomes. + Contribute to developing and implementing national sales campaigns and strategies for medium to large accounts. + continuously expand your understanding of current industry trends, competitive landscapes, and technical knowledge, sharing these insights with colleagues to foster informed decision-making. + collaborate cross-functionally with Marketing, Sales, and Supply Chain colleagues to align on product positioning, demand planning, and customer support strategies. + proactively identify opportunities to retain, extend, and acquire customers by devising and implementing tailored solutions. This is a field based role - the territory is within the Pacific Northwest Region. Ideal candidate to live within 50 miles of this geography and within 25 miles of a metropolitan airport. Travel expectation: 50% **Who You Are:** + Bachelor's Degree or equivalent experience + 5+ years relevant sales or equivalent experience **Preferred Requirements:** + Ph.D. in Molecular Biology, Genetics, Microbiology or related field + Demonstrated ability to influence and build strong consultative relationships with Key Opinion Leaders + Entrepreneurial spirit, strong business acumen, strategic planning and organization skills Relocation benefits are not available for this job posting The expected salary range for this position based on the primary location of Washington is $88,300.00-$164,100.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. 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 form Accommodations for Applicants (***************************************************************************************************** .

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 a member of Global Customer Support you will be supporting on-market products, performing advanced second-level troubleshooting, and provide guidance to junior members of the team on troubleshooting techniques and second-level inquiries. You will work consistently with cross-functional teams. You will lead team members and participates in and/or leads design reviews, and provides direction to junior members of the team on all elements of the project Charter in establishing service requirements on development projects. The GCS Sr. HW/SW Engineer is involved in defining the work scope and works autonomously with little to no supervisor direction. Serves as a technical expert on product(s) and works on complex projects requiring broad knowledge of products and systems. **The Opportunity:** **Key Responsibilities** + Acts as the primary GCS technical lead for resolving high-priority hardware/software development requests from the Development team. + Manages the frequency and urgency of incoming development requests to free the rest of the team for daily support jobs. + Provides expert-level HW/SW support during "rush hour" periods, including system support for regional and affiliate escalations. + In the role of a GCS Project Leader: Leads the overall GCS project team for new product development and updates, accountable to provide all GCS project deliverables on time, on quality, and within scope. + Represents GCS in relevant project meetings with the Development team to ensure that service and support needs are considered and implemented. + Provides on-market support by addressing complex Level 2 submissions independently with little or no direction. + Creates / revises curriculum for training sessions and provides new approaches to improve the training process. Delivers training to support internal staff readiness for launch. + Participates in and leads design review teams to provide service perspective, reviews and approves design change content, and creates the required deliverables. + Creates and updates service manuals and all service documentation for new product launch and on-market support. + Follows established Roche Quality System procedures in execution of work and identifies need for and creates new departmental procedures. + Other duties as assigned by management. **Who you are:** **Required Qualifications & Experience** Formal Training/Education: + **Formal Training/Education:** Bachelor's degree (in electronics, engineering, computer science, or similar technical degree) and 5 years of relevant technical support experience (customer-facing role and incorporating experience with troubleshooting and training) AND the experience would pertain to the installation, repair, assembly, and/or testing of electromechanical devices. Knowledge, Skills, and Abilities: + Applies advanced knowledge of hardware repair, networking and servicing principles, and practices. + Possesses good communication, organizational, logical thinking, and presentation skills. Communicates complex and unfamiliar ideas and solutions easily to users with little or no technical knowledge. + Ability to work independently on assigned tasks of broad scope with minimal guidance or supervision. + Ability to read and understand electrical, mechanical, and assembly drawings, diagrams, schematics, specifications and technical procedures. + Ability to use test equipment (e.g., digital multimeters) and various hand tools. + Courteous and customer-oriented. Works to satisfy internal and external partners. **Preferred Qualifications** + **Experience with Sequencing (Seq) instruments and NGS technologies/workflow is highly appreciated** . + **Demonstrated experience working closely with Development (Dev) teams** . + A plus: practical experience with Linux commands and the ability to navigate through the log files using CLI. + Project management experience. + Previous experience mentoring and/or training. **Travel Requirements/Location Requirements** + **Location:** Santa Clara, CA + **Travel time:** 25% both domestic and international, required + **This position does not offer relocation** The expected salary range for this position based on the primary location of California is $89,500 - $166,300.00. 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 form Accommodations for Applicants (***************************************************************************************************** .

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 PTT (MSAT & Engineering) is responsible for ensuring that PT stays at the forefront of technology in our facilities and supports our robust processes & efficient operations. We focus on integrating product health, process health with equipment fit for purpose, and facility readiness in support of the manufacturing network. Within PTT, Roche's global Manufacturing Science and Technology (gMSAT) department is the process and product owner for our commercial products, including our internal and external drug substance and drug product network, implementation of new technologies, network standardization, and mitigation of technical risks. The team is organized by product-focused Large Molecule and Small Molecule (DS & DP), Technology and Network Standards and Operations (Process Stewards, Tech Deployment, and Pilot Plant) teams and operates in cross-functional squads and circles. The Opportunity The Senior Large Molecule DP Product Steward is responsible for driving seamless technical industrialization and sustaining and improving the technical health of commercial products, starting from manufacturability decision through process performance qualification (PPQ), supply maturity and optimization, and ultimately divestment. Your main responsibilities cover Technical Industrialization (Develop Technical Strategic Roadmap) and Product Technical Health Management (Own & Mitigate Technical Risks) : * Identify, define, and deliver DS or DP-related technical industrialization strategies and technical improvements to ensure successful launch as well as that the product remains validated, robust, cost-effective, and compliant * Deliver on the product's technical strategic roadmap across the commercial lifecycle, as defined by an end-to-end Product Technical Lead, which includes investigating and mitigating technical risks, implementing improvements, and aligning strategies with broader network objectives * Serve as a primary product technical owner for site leadership and quality functions when investigating product or process issues across the commercial lifecycle * Represent the product in key technical governance forums and senior stakeholder interactions Who you are The ideal candidate is a recognized authority in the field, bringing scientific expertise, industrial experience, and leadership capabilities. * B.S. or M.S. degree in a scientific discipline (biotechnology, pharmacy, biology etc. ), with at least 7+ years of relevant industrial experience in platform specifics process development or in supporting platform specific manufacturing operations (e.g. DS Bio, DP SM etc.), PhD is of advantage * Proven record in Drug Product manufacturing and product and technology industrialization as well as process development in the field of biological molecules. * Demonstrated experience with technology transfer and/or with process validation and in pharmaceutical quality systems and industry-wide guidelines pertinent to platform specific process development and manufacturing * Strong understanding of regulatory submission and health authority requirements and of of patient needs / patient-centricity as key elements of design and delivery Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity! Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Basel. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. 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.

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** The Roche/Genentech Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late stage development (Phase 2-3) clinical strategies and plans to deliver medically differentiated therapies that provide meaningful improvement to patients. Alongside the Clinical Science Leader (CSL)/Global Development Leader (GDL), the Senior Clinical Research Scientist leads the development of the clinical science aspects of the Clinical Development Plan (CDP) strategy and supports various deliverables for effective and efficient CDP execution for the molecule/indication. The individual in this role will work very closely with colleagues to support late stage programs in the Obesity/Metabolic space. Senior Clinical Research Scientists perform their responsibilities with independence and with demonstrated leadership. **The Opportunity:** + You have demonstrated experience independently managing relationships with significant external partnerships/institutions (e.g. business alliance partners, academic institutions), in order to advance clinical programs) + You will provide oversight of Medical Data Review Plan execution, database lock, data interpretation and CSR and manage the process in the context of the broader CDP. + You have the ability to set out the strategy for trial/protocol development and context in the broader CDP to GDT/LCT, ensuring appropriate data are reflected in the protocol, ICFs and CSR. + You will establish the clinical science strategy for CTA/EC submissions, briefing packs and responses to HA questions and provide context with respect to the broader CDP to the filing team, GDT and other stakeholders. + You can act independently with investigators and oversight of investigator meetings. + You have experienced contributing to Therapeutic Area Expert interactions to optimize clinical programs (e.g. advisory boards, individual engagements, steering committees) **Who You Are:** **(Required)** + You hold a bachelor's Degree (life sciences); Advanced Clinical/Science Degree is highly preferred (e.g. PhD, PharmD, MSN, MPH, etc). + You have extensive academic and/or industry experience, with a primary focus in late stage clinical development; you have the ability to independently carry out the majority of their study conduct responsibilities and clear evidence of independence with respect to clinical science oversight and setting out the clinical science strategy to the clinical subteam. + You have strong knowledge of medical aspects of GCP (Good Clinical Practice), ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use), FDA, EMA and other relevant guidelines and regulations is required + You have in-depth knowledge of cross-functional teams involved in the drug development process and can integrate multiple perspectives into the CDP. Experienced in driving various aspects of cross-functional study level strategy, e.g. study design, supporting feasibility and timelines/budget projections, protocol amendment requirements. **Preferred:** + You have a proven track record of leading and performing in a fast-paced, matrix environment; ability to work independently and influencing others with strategic decisions + You have demonstrated experience working with a Study Management Team (SMT), including training, responding to clinical study queries and support on clinical activities + You have experience active as a co-lead in collaboration with various stakeholders, including study investigators. + You have experience leading and mentoring others + You have experience solving unique or unpredictable problems that might have an impact on the goals and objectives as set by the organization + You have the ability to partner across diverse regions, cultures, and time zones to create an environment of belonging, inclusion and diversity. + You have demonstrated Interpersonal skills: Strong verbal communication and influencing skills; can influence without authority and has proven experience building and cultivating relationships with key partners and stakeholders, both internally and externally **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.**

Genentech, Inc. seeks a Senior Data Scientist (Quality Excellence Lead) at its South San Francisco, CA location. Duties: Description: Review and analyze inferences made on clinical study data by the Quality Audit team and present statistics based opinions to check for clinical quality compliance using R, Python and Amazon Web Services (AWS) packages. Provide analytical expertise in clinical data quality, improvement opportunities, and understanding of variations in the clinical study data and quality metrics. Use descriptive and advanced analytics such as machine learning, statistical models and natural language processing techniques to identify data points of interest and trends in clinical study data and conducts a risk assessment to the quality impact factors. Assess clinical data before study audits and health authority inspections (Food and Drug Administration (FDA)/EMEA) to mitigate potential risks. Use statistical analysis to identify improvements and opportunities for clinical quality gap closure and determine the methods of analytics that needs to be used after carefully evaluating the clinical data and client requirement. Identify appropriate methodologies by writing code to statistically analyze output to provide subject matter expertise on clinical quality metrics development to analyze and report on quality measures. Identify raw data in clinical systems such as electronic case report forms (eCRFs), financial disclosure forms etc. and conducts data wrangling to check for data consistency and identifies inaccuracies within the data using Python, R and AWS packages and visualizations using Tableau. Conduct analysis to assign weights to features within large clinical datasets to use for prospective predictive analytics and deep learning projects. Work with the Quality team to iteratively validate data using R, Python, Machine Learning, Artificial Intelligence, Natural Language Processing, techniques and develops visualizations using Tableau to present results to team. Work with auditors to present case studies of the use of analytics in clinical trial - quality assurance at international conferences like DIA etc. Review and analyze data from multiple internal/external sources to create dashboards, drill down reports and key quality performance indicators. Education/Experience Requirement: Master's degree in Data Analytics, Data Science, or related field, and 1 year of experience as a data scientist or analyst, clinical data manager or analyst, or related role. Specialized Experience: Position requires 1 year of experience with the following: Clinical study data standards including Clinical Data Interchange Standards Consortium (CDISC) and Standard Data Tabulations Model (SDTM); Good Clinical Practices (GCP) Clinical Trial Process and documentation, Investigator Brochures, Protocols, Informed Consent Forms; Collection and maintenance clinical data systems such as electronic data captures systems, electronic trial master systems and clinical trial management systems; Quality and Good Clinical Practices (GCP) relating to Clinical Trial Process and associated documentation i.e., Investigator Brochures, Protocols, Informed Consent Forms; Clinical study quality auditing experience. Position requires 6 months of Applying Statistical Models to clinical study data. Worksite: 1 DNA Way South San Francisco CA, 94080 The expected annual salary range for this position based on the primary location for this position of South San Francisco, California is $172,008.00 to $221,000 per year. Actual pay within the range 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 **************************************************** Apply (insert link)(Job ID) Genentech 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 form Accommodations for Applicants.

Genentech, Inc. seeks a Data Analyst II at its South San Francisco, CA location. [[[system test]]] Duties: Work with Genentech's US Patient Safety team's internal business stakeholders (Pharmacovigilance (PV) Operations & Innovations, Market Research & Patient Support Programs, and PV Clinical teams) to assess and clarify requirements/specifications for safety-related data query, to provide programming solutions, and to ensure their efficient implementation. Design, develop and implement predictive models in Python and/or R using machine learning algorithms and forecasting techniques for Genentech's AE monitoring system. Validate and fine-tune models to ensure accuracy and reliability to support decision making processes. Define and implement sampling methodologies and use the output to develop key metrics and performance indicators. Requirement of strong analytical skills to translate sample data into actionable insights. Develop and implement data visualization using large, complex datasets in Tableau to provide actionable insights. Ensure the accuracy and effectiveness of visualizations by conducting thorough testing and validation by utilizing data analytics' best practices. Design and develop automated solutions using R, Python, and/or SAS, to expedite programming activities and usage for data management and data review. Identify and recommend PV system process improvements and automation within data workflows. Analyze current practices, pinpoint inefficiencies, and design solutions to streamline operations, reduce manual effort and enhance data accuracy. Develop and review specification documents for data analysis and coding projects. Require strong understanding of translating business requirements into detailed technical specifications for models and analytics solutions. Build and monitor quality utilizing data analytics' best practices in every aspect of job activities in Genentech's US Patient safety team. Education and experience required: Master's degree in Business Analytics, Mathematics, Statistics or related quantitative field, and 4 years of experience in advanced data science and business analytics role Special Requirements: Must have 4 years of work experience with each of the following: Designing, implementing and fine-tuning statistical and machine learning prediction models in Python and/or R. Using SQL for querying and managing large, complex datasets. Using Tableau and/or Power BI to develop interactive dashboards and reports to effectively communicate data findings and trends. Developing and implementing time-series forecasting models in Python and/or R. Leveraging programming languages such as Python, R and/or SAS to reconcile, manipulate and test accuracy of data, and to analyze and visualize complex datasets, create automated processes, and develop scalable workflows Providing consultation to users in the area of automated systems and leading cross-functional teams to address business or systems issues. Designing and implementing sampling strategies (random, stratified, systematic, etc.) to ensure representative data collection and applying statistical inference techniques such as hypothesis testing to draw meaningful conclusions. Designing and deploying machine learning and forecasting algorithms such as Clustering, Logistic Regression, XGBoost, ARIMA and SARIMA models. Working with relational databases such as Teradata and Oracle. Must have 1 year of experience within the Pharma/Biotech industry. The expected annual salary range for this position based on the primary location for this position of California is $204,214 to $268,800 per year. Actual pay within the range 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 (**************************************************** Worksite: 1 DNA Way, South San Francisco CA, 94080 Genentech 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 form Accommodations for Applicants.

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 Digital Pathology Sales Specialist The Opportunity: We are seeking a driven Digital Pathology Sales Specialist to champion the sales of our comprehensive digital pathology solutions. This includes hardware, Image Management Software (IMS), and advanced algorithms, targeting a diverse client base: hospitals, reference labs, research institutions, pharmaceutical companies, and diagnostic labs. The ideal candidate will possess a deep understanding of digital pathology products, healthcare IT, and strong sales acumen. You will be instrumental in building and nurturing relationships within the healthcare and research sectors, leveraging existing connections to expand our customer base. This is a specialist position supporting the Account Managers and Strategic Account Managers which is key to engaging both prospective and current customers. This is a field based role: the territory includes all of California (main hubs: Los Angeles, San Francisco, San Diego). Candidate must reside within 50 miles of territory border and near a major airport. Relocation benefits are not provided for this role. Key Responsibilities: Sales and Business Development: * Achieve and exceed sales quotas by developing a robust pipeline and closing new business. * Develop and execute strategic sales plans to significantly grow the company's market share in digital pathology. * Present and demonstrate digital pathology solutions to potential clients, clearly articulating the value proposition of transitioning to digital workflows. * Identify potential customers, understand their specific needs, and present tailored solutions. * Maintain accurate records of all sales activities, customer interactions, and sales opportunities within the SFDC system. * Provide regular sales forecasts and reports to the regional sales manager, actively participating in sales meetings. Technical Expertise & Customer Advisory: * Cultivate deep technical expertise in our software to accurately map and align its applications with relevant disease areas. * Act as a trusted advisor to clients, thoroughly understanding their pathology workflows and providing customized solutions. * Address customer inquiries, resolve concerns, and ensure exceptional customer satisfaction throughout the entire sales process. * Achieve high levels of customer satisfaction through effective sales and support assistance. Collaboration & Support: * Collaborate closely with technical teams to provide compelling product demonstrations, training, and ongoing post-sales support. * Coordinate product demonstrations, installations, and customer training as required. * Partner with customer service, technical support, and Roche Healthcare Consulting to guarantee seamless post-sales implementation and support. Industry Knowledge: * Stay continuously informed about industry trends, competitive products, and emerging technologies within the dynamic digital pathology space. Key Performance Indicators (KPI's) * Achieve and exceed monthly, quarterly, and annual sales targets. * Increase market share for digital pathology products in assigned region * Establish and maintain a pipeline of prospects. * Customer satisfaction scores and retention rates. Who you are: * You hold a Bachelor's Degree in a related field (Life Sciences. Biomedical engineering, biotechnology or similar) or equivalent experience * You hold 3+ years of experience in sales, preferably in digital pathology, medical devices, healthcare IT software, or life sciences or equivalent experience. * Leadership presence and business acumen with an understanding of digital pathology systems and their software applications in clinical and research settings. * You hold have proven success in previous sales capacity, using consultative selling skills, along with demonstrated leadership and communication excellence. * Presence and communication ability required with the ability to create and present impactful group presentations. * Negotiation, contracting, and problem solving skills Preferred: * Laboratory sales experience, healthcare IT * Experience/background in IT or technology sales * Digital Pathology The expected salary range for this position based on the primary location of CA is $100,400 - $186,400. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below. Benefits #LI-JW2 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 form Accommodations for Applicants.

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** Are you ready to make a real difference in the world of Safety, Health, and Environmental (SHE) management? As a SHE Business Partner, you'll step into a role where you'll leverage your expertise to drive impactful programs across functional areas such as Manufacturing, R&D, Facilities, and Supply Chain. This dynamic position combines problem-solving, policy development, and thought leadership to create safe, sustainable, and compliant environments within a leading-edge organization. With the opportunity to serve as a trusted advisor to leadership, spearhead complex projects, and lead innovative initiatives, you'll play a vital role in shaping and enhancing SHE programs that support compliance, sustainability, and operational excellence. If you're passionate about driving change and thrive in a position of leadership, this opportunity might be your next career step. **The Opportunity** Functions as a Safety, Health, and Environmental (SHE) Business Partner for assigned functional areas (e.g. Manufacturing, Facilities, R&D, Supply Chain, etc.). In addition, will fulfill multi-site responsibilities for specific program area ownership. Expected to work on projects across the business functions, business units, and our business area. Applies extensive knowledge and skills to complete a wide range of difficult tasks. Acts independently to determine methods and procedures on new assignments. Consults with management in the understanding of policies, procedures, programs, and company directives to ensure compliance. Duties are diverse and complex often involving research, analysis, and solution development. Possesses and applies a comprehensive knowledge of a particular field across multiple business functions. Plans, conducts and oversees work involving large and important/complex projects. May provide direction and guidance to more junior SHE staff. Reviews progress with management. Serves as a recognized resource to multiple Roche sites, corporate management, and/ or cross functional teams. May serve as a resource to all levels of personnel across our business area, including other Roche locations and assist external customers as needed. Works with considerable independence to provide direction and guidance on issues to department leadership, business functions, and/or SHE staff members. **Responsibilities:** + Coordinates, develops, implements, and maintains SHE policies, procedures, and programs for regulatory programs, company-specific Directives and Standards, Bay Area-wide goals, and other company initiatives and requirements within assigned areas of responsibility. Bay Area program management responsibilities may include (but not be limited to) Hazardous and Biohazardous Waste, Industrial Hygiene, Compressed and Asphyxiating Gases, Chemical Safety/HMBP, and Wastewater. Site program management responsibilities may include a variety of other physical safety, environmental and health programs. + Facilitates across multiple business functions, units, and/or our business area in order to help management establish objectives and plan SHE compliance and sustainability programs to achieve objectives. + Serves as the subject matter expert in the implementation of one or more program areas. Leads the identification of programs that need improvement. Creates and leads teams to address deficiencies. + Provides expertise to both management and lower level positions. Assists management and staff in resolving difficult technical problems, interpreting laws, regulations and Roche Directives and Standards. Assist management with new staff orientation and training as well as developing staffs' ability to achieve total impact recognition. + Conducts analysis of key program areas or as assigned by management. Analyzes trends, makes monthly, quarterly and annual comparisons. Works with vendors, staff and applicable business functions to identify opportunities, implement initiatives, and maintain program execution. Establish/improve the company's ability to track, measure, and report on assigned activities. + Identifies opportunities for improvements in current systems, works with area management for change, implements changes, monitors progress and refines systems. + Proactively inspects and conducts hazard evaluations of work areas related to subject matter expertise. Assesses impacts associated with equipment, materials, processes, and facilities; in order to identify and control hazardous conditions or actions that may cause adverse impacts and/or regulatory non-compliance. + Develops, implements, and conducts formal campus wide SHE inspections and audits. Assist with or lead external audits as required. Tracks resolution of issues. + Participates in emergency planning and emergency teams. Responds to emergency situations as needed. + Supports SHE management with projects or activities as assigned, which have impact across Molecular Solutions, Roche Divisional, and/or Corporate functions. + Other duties as assigned by management. **Who you are** **Qualifications:** + Bachelor degree in in physical science, life science, environmental sciences, engineering, safety, industrial hygiene, or other relevant field. + Master's degree preferred. + Completion of a national certification, or ability to obtain, such as Certified Industrial Hygienist (CIH) or, CHMM (Certified Hazardous Materials Manager) or, Associate Certified Safety Professional (ASP), Certified Safety Professional (CSP) or Professional Engineer (PE) preferred. **Experience:** + 10-12 years of experience in administering safety, health & environmental programs, preferably in a biotech, pharmaceutical, diagnostics, chemical or relevant industry required. **Knowledge, Skills, and Abilities:** + Ability to influence opinions and decisions of SHE activities beyond local site. + Ability to replicate best practices across business functions and/or business units. + Ability to evaluate existing knowledge sharing within Roche and replicates or influences those having positive/negative impact to the site. + Knowledge, interpretation, and application of laws and regulation and the ability to identify issues and make sound decisions under conditions of risk and uncertainty. + Proven background to identify, learn, develop, implement, and sustain new areas of subject matter expertise. + Excellent written and verbal communication skills: Written (business email, technical documents, programs) and verbal (leading meetings, presentation, and training). + Highly proficient computer skills (Microsoft office suite; Google Docs, Gmail, etc.) This position is not eligible for relocation. The expected salary range for this position based on the primary location of California is $99,80000 - $185,400 USD Annual. 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 form Accommodations for Applicants (***************************************************************************************************** .

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** Our team is composed of forward-thinking scientists, engineers, and researchers who are passionate about revolutionizing healthcare through innovation. We are seeking a highly motivated and experienced Software Engineer to join our growing team and contribute to the development of high-performance, high-quality NGS bioinformatics algorithms. **The Opportunity:** As a Software Engineer specializing in Next Generation Sequencing Bioinformatics at Roche Diagnostics, you will play a critical role in designing, developing, and optimizing cutting-edge algorithms to extract meaningful insights from genomic data. This position offers a unique opportunity to work on innovative projects that impact the fields of diagnostics and precision medicine. You will work closely with cross-functional teams of biologists, data scientists, and software engineers to build robust, scalable, and efficient software solutions. + Algorithm Development: Design and implement high-performance algorithms for NGS data analysis, including variant calling, quality control, and data preprocessing. + Optimization: Continuously refine and optimize bioinformatics solutions for handling large-scale genomic datasets with improved efficiency and performance. + Collaboration: Partner with biologists, data scientists, and engineers to meet the unique challenges of NGS diagnostics and research workflows. + Software Integration: Seamlessly incorporate bioinformatics tools into Roche's software ecosystem, ensuring compatibility and robustness. + Quality Assurance: Maintain the integrity of analytical results by crafting rigorous test suites and working alongside QA teams. + Innovation and Leadership: Stay at the forefront of NGS and bioinformatics trends while mentoring junior engineers and driving innovation within the company. **Who You Are:** + You hold a Bachelor's or higher degree in Computer Science, Bioinformatics, Computational Biology, or a related field. + You have at least 8-10 years of proven experience in developing high quality software and algorithms for NGS data analysis. + You have strong proficiency in programming languages such as C++ and Python. + You have a track record of proficiency in relevant bioinformatics tools and libraries. + Demonstrated progression in experience with parallel computing, optimization, and performance tuning. + You have strong problem-solving skills and attention to detail. + You have excellent communication and teamwork skills. **Preferred Qualifications:** + Experience working in a regulated environment (e.g., FDA, CLIA). + Experience with GPU development and optimization. The expected salary range for this position is based on the primary location of Pleasanton, CA is $189,200 - $270,300. 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 in this **link (*************************************************** .** **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 form Accommodations for Applicants (***************************************************************************************************** .

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 Sequencing Solutions, Inc. seeks an International Product Manager at its Pleasanton, CA location. Duties: Apply knowledge of biological science, and confer with scientists, laboratory manager, key opinion leaders, and functional subject matter experts in the areas of non-invasive pre-natal testing (NIPT) and other women's health products, to plan and implement product marketing and branding strategies and projects. Serve as a subject matter expert for Roche's NIPT and other women's health products. Provide training, tools, and high-level support for product issues for regional representatives and/or affiliates. Contribute commercial ideas into planning for product research and development, applying understanding of how molecular, sequencing, and micro-array products are designed, manufactured, and commercialized. Provide key feedback that guides research and development of molecular tools, including NGS and micro-array reagents, automated instrument compatibility, bioinformatics pipelines, and analysis and interpretation software, for NIPT and other women's health products. Guide appropriate market research and analysis of the global market for NIPT and other areas of women's health. Participate in and coordinate the development of marketing tools and globally organized marketing activities in support of the products, considering relevant regulatory rules and guidelines and their impact, as well as providing message development and communication of product positioning and branding. Identify portfolio gaps and make recommendations. Identify and monitor competitor activities and help to develop product feature decisions that scientifically differentiate our products, taking into account the highly competitive landscape of NIPT and women's health products. Create the customer requirements that will be used to create and drive the direction of our research and development, as well as our global marketing and branding strategy, for the NIPT and women's health portfolio. Contribute to and update the relevant chapters of Customer Requirements Document (CRD). Generate proof sources, including studies and publications, application notes, and white papers, that show how our products work and can be used and what type of data they generate. Drive the fulfillment of regulatory, market access, and commercial requirements needed to ensure that the products developed can be sold in all major international, regulated, and unregulated markets. Manage allocated product budget. Requires 25% domestic and international travel. Up to 2 days per week telecommuting allowed. Education and experience required: Bachelor's degree or foreign degree equivalent in Marketing, Life Science, or a closely related field, and 2 years of experience as a Service Portfolio Liaison, in the job offered or a closely related role. Special Requirements: Employer requires 2 years of experience in the following areas: 1. Developing product strategy, including marketing strategies in the areas of genetics, molecular biology, and bioinformatics 2. Analyzing market trends, competitive landscape, and customer needs to identify opportunities for product differentiation, pricing strategies, and market positioning against competition for the success of the product 3. Collaborating with various business, technical, and scientific teams to create customer requirement documents, plan product roadmap, and scope priorities and resources to meet established objectives 4. Utilizing assay, reagents, and microarray technology to manage on-market product needs, manage customer complaints, and develop roadmap and project scope for launching product improvements 5. Collaborating with various business, technical, and scientific teams to ensure customer satisfaction, prevent interruptions to the business in the field, and ensure that appropriate steps are being taken to ensure feasibility of on-market product 6. Using SAP, SalesForce, Tableau, Microsoft Suite, and Quality management Systems to manage inventory and approve documentation in compliance with regulatory bodies 7. Working within applicable regulatory frameworks to ensure product is compliant Requires 25% domestic and international travel, fully-reimbursed. Up to 2 days per week telecommuting allowed. Worksite: 4300 Hacienda Drive, Pleasanton CA 94588 The expected annual salary range for this position based on the primary location for this position of Pleasanton, California is $182,112 to $245,200 per year. Actual pay within the range 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 form Accommodations for Applicants.

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** The GCS Senior Specialist is the third in the series of four jobs. The employee is involved in defining the work scope and works autonomously with little to no supervisor direction. Serves as a technical expert on customer IT/Network design and works on complex projects requiring broad knowledge of sequencing data systems. **The Opportunity:** **Key Responsibilities** + Provides on-market support by addressing complex Level 2 network/IT submissions independently with little or no direction. + Analyzes and understands customer use cases, bioinformatics (BFX) pipelines, and application (App) data flow to define infrastructure requirements. + Develops, documents, and iterates on comprehensive IT/Network guidelines for customer sites, including detailed plans for data storage and bandwidth capacity. + Leads the global customer-site readiness process from an IT/Network perspective, ensuring all preparations are complete prior to customer installations. + Creates, revises, and delivers curriculum for training sessions for affiliate teams on customer room readiness, network design, and IT guidelines. + Participates in and leads design review teams to provide an IT/Network service perspective, reviews and approves design change content, and creates the required deliverables. + Creates IT/Network service requirements on development projects and advocates for functional goals. + Responsible for creating and updating service documentation, service manuals, and technical bulletins related to network/IT setup, configuration, and troubleshooting. + Follows established Roche Quality System procedures in execution of work and identifies need for and creates new departmental procedures. + Utilizes project management fundamentals to ensure assigned projects are completed properly and on time (with potential to lead GCS projects as a TPM). + Other duties as assigned by management. **Who you are:** **Required Qualifications & Experience** Formal Training/Education: + Formal Training/Education: Bachelor's degree (in Computer Science, Information Technology, Engineering, or similar technical degree) and 5 years of relevant technical support or IT infrastructure design experience (customer-facing role and incorporating experience with troubleshooting and training). Knowledge, Skills, and Abilities: + Advanced knowledge of enterprise networking, IT infrastructure, data storage solutions (NAS/SAN), and bandwidth planning principles. + Strong understanding of customer IT environments, preferably in a diagnostics, life science, or regulated setting. + Possesses good communication, organizational, logical thinking, and presentation skills. Communicates complex and unfamiliar ideas and solutions easily to users with little or no technical knowledge. + Ability to work independently on assigned tasks of broad scope with minimal guidance or supervision. + Normally receives little instruction on day-to-day work, determines methods and procedures on new assignments. + Ability to interact with appropriate internal cross-functional groups, areas, and regions. + Courteous and customer-oriented. Works to satisfy internal and external partners. **Preferred Qualifications** + Demonstrated knowledge of bioinformatics (BFX) workflows and sequencing applications (App). + Experience with Sequencing instruments and NGS technologies/workflow. + Practical experience with Linux commands and navigating log files using CLI. + Project management experience. + Previous experience mentoring and/or training. **Travel Requirements/Location Requirements** + **Location:** Preferred in Bay Area, CA. Will also consider RDI or Penzberg. + **Travel time:** 25% both domestic and international, required. + **This position does not offer relocation.** The expected salary range for this position based on the primary location of California is $89,500 - $166,300.00. 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 form Accommodations for Applicants (***************************************************************************************************** .

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 At Roche/Genentech, we believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives and making medicines more convenient and accessible to patients while investing in our planet to reduce the carbon footprint. We are fearless in both decision and action. That is why we come to work each day. Who We Are Pharma Global Technical Operations (PT) is the organization that manufactures and delivers Roche's groundbreaking therapies to millions of patients worldwide. PT is involved in producing every Roche medicine from the development process through clinical trials and continuing to product maturity. Our organization coordinates all aspects of the production of Roche medicines in all disease areas and dosage forms. Pharma Technical Development (PTD) is an integral part of this mission. As an organization of over 2,500 people globally, PTD is responsible for developing the manufacturing processes, products, analytical methods, and Chemistry, Manufacturing & Controls (CMC) strategies to deliver all new products in Roche's pipeline. This work encompasses the full range of development functions, including biologics, synthetic molecules, devices, clinical supply chain management, and project and portfolio management. PTD applies leading technical expertise to design, develop, supply, and register clinical-stage products globally, reliably delivering the pipeline and supporting commercial manufacturing operations. We excel through innovation, collaboration, dedication, and mutual respect, continuously improving what we do to ensure Roche's supply of quality products to patients. We commit ourselves to scientific rigor, technical excellence, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. The Opportunity The Global Head of Project and Portfolio Management will provide strategic and operational leadership for Chemistry, Manufacturing & Controls (CMC) across the R&D organization. You will define and drive the global CMC development portfolio and strategy, ensuring alignment with corporate priorities, scientific innovation, and regulatory expectations. Additionally, you will oversee portfolio execution, CMC project management, and a team of technical development leaders (CMC leaders) responsible for delivering high-quality, timely CMC packages to advance the pipeline from early development through commercialization. Key Responsibilities CMC Strategy & Leadership * Establish and lead the global CMC development strategy in alignment with One Pharma Strategy and R&D Excellence objectives. * Anticipate and integrate industry, regulatory, and scientific trends into CMC approaches and portfolio decisions. * Provide scientific, technical, and business leadership to guide critical CMC development programs. Portfolio Management & Execution * Develop, enhance, and oversee CMC portfolio governance, prioritization, and decision-making processes effectively such as Late Stage Technical Development Committee (LSTDC). * Ensure timely and efficient delivery of CMC packages supporting IND, CTA, IMA/BLA/NDA, and global submissions. * Drive portfolio insight and performance analytics to optimize resource allocation and execution. * Lead the creation and use of standard systems, tools, and processes to enable analysis and management of the technical development portfolio (e.g. 100 people years, RDE DevGo to EIH goal). Project & Program Leadership * Manage CMC strategies, risks, and overall project execution to efficiently deliver robust manufacturing processes and materials within requested timelines and budget * Partner with R&D, regulatory, quality, clinical, and commercial & PT stakeholders to ensure seamless development collaborations and execution. * Champion a culture of operational excellence, accountability, and proactive risk identification and mitigation. Team Leadership & Talent Development * Lead, inspire, and develop a team of technical development leaders (TDLs) delivering the projects by working with functions such as drug substance, drug product, analytical development & quality control, device and delivery, regulatory CMC, manufacturing sciences, and clinical and commercial manufacturing sites. Act as a coach for teams. * Recruit, retain, and develop high-potential talents for the Technical Development Leaders (TDLs) and Project Managers. Foster a high-performing, collaborative, and inclusive culture. * Build organizational capabilities to meet evolving portfolio and industry needs. Leadership Team Contribution * As a member of the PTD leadership team, contribute to the team's high performance, foster cross-functional thinking, and work collaboratively to set priorities for the global organization. Stakeholder Engagement and Communication * Ensure a strong connection to key stakeholders within the broader global project team system (e.g., Lifecycle Teams, gRED & pRED project Teams). * Partner with R&D, regulatory, quality, commercial stakeholders, and Roche Partnering to ensure seamless development transitions and alignment. * Enable open and timely communication with senior management regarding CMC issues and resolutions. Facilitate project status reports, governance committee briefings, and project updates to management. Who You Are * Advanced degree (Ph.D. preferred) in chemistry, biology, engineering, pharmaceutical sciences, or related discipline. * Extensive years of progressive and inspiring leadership in CMC development, manufacturing sciences, or related R&D functions, with proven success and a long track record. * Deep knowledge of global regulatory requirements, product development processes, and CMC and/or product lifecycle management. * Demonstrated ability to grasp the changing and dynamic external environment to shape strategy, manage complex portfolios, and deliver across early and late-stage development. * Exceptional leadership capabilities, excellent communication-, and influencing skills in effective engagement with leaders and stakeholders across R&D and PT. Ability to positively influence colleagues and key decision-makers. * Strong business acumen and collaboration skills, with the ability to balance scientific, operational, and strategic priorities in a global organization. * Experience in team leader development, project portfolio management, and developing business processes and tools to support a global team system. * 15-20% international travel required. Leadership Competencies * Strategic and innovative thinker with a global mindset. * Strong decision-making and problem-solving skills in complex, fast-paced environments. * Track record of building and leading high-performing, inclusive teams, passionate about talent development. * Highly collaborative, able to influence and align across all levels, internal stakeholders, and external partners. * Commitment to quality, compliance, and patient-centric innovation. 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.

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 a Software Solution Program Management Lead, you will drive the software project management activities related to the launch and further development within the Roche Sequencing Platform. This includes coordinating the work across research and development teams along the sequencing datapath - instrument control, real time analysis, platform management, and downstream post-primary analysis software. Success will require providing software project management leadership across the solution with the goal of a cohesive sequencing commercial launch. **The Opportunity:** + You will be accountable for the overall planning, execution tracking, and coordination of the software datapath for the sequencing solution by managing and optimizing the flow of the various sequencing software solution projects using various tools, such as the program JIRA boards, Gantts, etc. + You will oversee the sequencing software solution team progress updates with regards to execution & testing of features and capabilities. You will consolidate and report status to the Sequencing Core Team, Steering Committee, and various project teams. + You will hold Product and Project Managers accountable for aligning of planned actions with the overall solution delivery strategy + You will provide input on resourcing to the Sequencing Core Team and the capabilities needed to address critical bottlenecks + You will work with the various software teams to define solution integration configurations, checkpoints, and installations + You will manage stakeholders within the sequencing software project and solution teams. and also with internal and external research partners. + You will develop / modify processes, policies, and procedures to facilitate the working relationship between software development teams and its business functions / partners. + You will ensure compliance with Roche processes, quality, and regulatory requirements. **This is an onsite position based in Santa Clara, CA** **.** **Relocation support will not be provided.** **Who You Are:** **(Required)** + You have a Masters in computational science or related disciplines (e.g. mathematics, physics, computer science). + You have 8+ years leading complex projects or cross-functional teams in the Diagnostics, Medical Device, and/or Pharmaceutical industry. + You have first-hand experience delivering digital solutions in healthcare or life sciences (e.g. medical imaging, bioinformatics, ML/AI-driven clinical decision support). + You have a deep technical understanding of computational science and informatics applications and methods in the Diagnostics, Medical Device and/or Pharmaceutical industry. + You have demonstrated knowledge of hardware and software product development processes for regulated medical devices. **Preferred:** + You have the ability to manage complex projects with ambitious timelines in high pressure circumstances. + You have the ability to lead by influence. + You have strong meeting facilitation capabilities. + You have the ability to coordinate project related activities; the ability to challenge management in relation to data and resources. + You have excellent communication skills with ability to effectively present complex problems or projects to stakeholders of all levels across multiple functions. + You have high emotional intelligence, self-motivation, and strong analytical and interpersonal skills. The expected salary range for this position based on the primary location of Santa Clara, CA is $169,000 - $314,000. 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 form Accommodations for Applicants (***************************************************************************************************** .