Hoffmann-LA Roche Inc 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.

Genentech, Inc. seeks a Business Process Analyst at its Oceanside, CA location. Duties: Contribute to the design and development of solutions and continuous improvement of SAP/MES integration strategy and scenarios for manufacturing sites. Drive the Manufacturing Execution System (MES) integration strategy to align with organizational objectives. Forge strategic partnerships with the MES Program Lead, Product Line Lead, and Product Manager to shape and drive the Global MES Program Strategy. Pioneer innovative pathways with Product Line Leads and Product Managers in the new modalities space, integrating groundbreaking technologies into the Global MES Program Technology landscape. Collaborate with MES Core Teams to enhance the efficiency and effectiveness of MES solution deployment across sites. Lead rigorous testing initiatives, working directly with site teams to ensure the reliability, efficiency, and precision of MES/SAP solutions in alignment with business goals. Optimize SAP configurations, coordinating with master data and functional consultants to tailor data setups and configurations for seamless testing and implementation. Align global processes with strategic vision, partnering with the Global Business Process Harmonization team to ensure MES/SAP solutions adhere to the global Roche template. Deliver actionable insights and innovative guidance on adopting SAP S4/HANA/EWM and MES solutions to elevate site operations. Collaborate with MES integration product teams to rigorously test and enhance the MES-SAP interfaces, ensuring seamless system interoperability and superior functionality. May telecommute up to 3 days per week. Position requires up to 25% fully reimbursed domestic and international travel. Education and experience required: Bachelor's degree, or foreign equivalent, in Engineering or Computer Science or related field and 8 years of experience as Systems Engineer, Business/Systems Analyst, or related position Special Requirements: 3 years of experience must include: Pharmaceutical Manufacturing Processes SAP-MES interfaces Installation and deployment of Pharmasuite and Syncade Solutions Architecture Hands-on SAP Powershell Scripting The expected annual salary range for this position based on the primary location for this position of California is $181,128 to $267,700 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 Antibody Way, Bldg. 331, Oceanside, CA 92056 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** **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** 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** 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 (***************************************************************************************************** .

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.**

Job Posting: Vertex Fellows ProgramLocation: San Diego, CAFlex Designation: On-Site DesignatedStart Date: August/September 2026Application Deadline: January 9, 2026, by 5:00 PM ETPlease submit a CV/resume and cover letter with your application. Letters of Recommendation will be requested if invited to interview. About the ProgramThe Vertex Fellowship is a unique, one-year training program for outstanding scientists and physicians passionate about solving unmet medical needs and advancing transformative science. Fellows join Vertex for a customized post-doctoral experience, gaining hands-on experience with real-world R&D challenges and benefiting from mentorship by Vertex leaders.This program is designed to provide participants with a broad understanding of the science and business of drug discovery.Program Highlights Project-based Fellowship: Embed for one year within a Vertex project team Work on a project of relevance, based on your skills and our pipeline needs Training & Mentorship Intensive didactic training on the science and business of drug development Scientific mentorship from research leaders Career mentorship from Vertex leaders Exploring Career Fit Upon completion, participants will be able to effectively decide if a career in industry is the right fit, and if so, how they might develop their career Why be a Vertex Fellow? Contribute to transformative medicines: Help patients by advancing scientific ideas in a team-based environment Accelerate your career: Learn about drug discovery and build your professional network Mentorship: Receive guidance from scientific, medical, and business leaders at Verte Vertex Fellows Network: Develop connections internally and externally Program Timeline Applications Accepted: November 24, 2025 - January 9, 2026, by 5:00 PM ET Interview Invitations: February 2026 (Letters of Recommendation requested at this time) Interviews: Early March 2026 Formal Offers: Mid-late March 2026 Program Start: September 2026 Program End: August 2027 Eligibility Requirements PhD, MD, or joint degree attained within 0-5 years Demonstrated scientific impact (e.g., peer-reviewed publications, presentations, awards) Evidence of creative thinking, scientific problem solving, and innovation Interest in learning how scientific research leads to the development of therapies Application InstructionsPlease submit your CV/resume and cover letter by January 9, 2026, 5:00 PM ET.In your cover letter, consider addressing: Your most significant scientific or research achievement and how you accomplished it An example of how you applied creative thinking to solve a problem What you hope to gain from the Vertex Fellows Program Letters of Recommendation will be requested if invited to interview. Pay Range: $110,000 - $165,000 Disclosure Statement: The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more. Flex Designation: On-Site Designated Flex Eligibility Status: In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility. Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time. #LI-Onsite Company Information Vertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

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 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 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. At Roche Diagnostics, we are driven by our vision: innovating diagnostics, shaping healthcare, and changing lives. We are excited to see this vision come to life. The opportunity Join our team as the Global Strategic Pricing leader in the Diagnostics Global Access & Policy (GA&P) team. You'll play a vital role in developing strategic global pricing guidance for our products and solutions, collaborating closely with global, regional, and local teams to optimize revenues and ensure sustainable access. Be part of shaping our global pricing strategy and policy for a brighter future. Your impact: * Lead the design and implementation of global value-based pricing strategies for prioritized pipeline and on-market products, utilizing analytics to assess elasticity, forecast trends, and manage profitability. * Co-lead the roll-out of pricing strategies, including innovative pricing and contracting solutions, in collaboration with access and commercial stakeholders to drive market access and profitability. * Act as the main responsible for exception management, providing clear guidance and supporting affiliates with local strategy development to address access barriers. * Be the key responsible for price monitoring and insights generation using internal databases (e.g., DIAprice, sCORE), delivering actionable insights to affiliates, regions, and IBTs. * Establish and lead pricing committee meetings, issue price memos, and drive pricing governance, including the maintenance and monitoring of pricing policies, controls, and KPIs (e.g., floor price). * Conduct and leverage primary and secondary payer, reimbursement, and pricing research to inform global strategy and provide consolidated pricing and reimbursement advice to relevant product teams. * Partner cross-functionally to inform IBTs and their Product Managers on recommended price setting, ensuring adherence to relevant governance processes. Who You Are * Minimum 8-10 years of professional experience with recognized expertise in pricing and reimbursement, preferably in the diagnostics, medical device, or pharmaceutical industry. Affiliate and/or regional experience is a plus. * Possess a Bachelor's Degree in a relevant field such as business, finance, economics, health economics, life sciences, or public health. An MBA or other Graduate/higher-level Degree is beneficial. * Deep financial and commercial understanding with in-depth knowledge of the global reimbursement environment, competitive intelligence, and market segmentation for effective global price setting. * Demonstrated Strategic & Analytical Acumen with strong influencing, negotiation, and Agile leadership skills to excel in a global matrix organization and lead diverse multicultural teams. * Committed to permanently optimizing processes to increase quality and efficiency standards and implement pricing competence and awareness across the organization through training and support. Essential Skills * Strategic & Analytical Acumen: Must be able to design and implement global value-based pricing strategies, utilizing analytics to assess elasticity, forecast trends, and manage profitability. Deep financial and commercial understanding is critical. * DX & Market Knowledge: Needs in-depth knowledge of the global reimbursement environment, and the clinical value proposition of the products. Expertise in competitive intelligence and market segmentation is essential for effective global price setting. * Global Leadership & Execution: Must excel at cross-functional collaboration and stakeholder management across a global matrix organization. Key capabilities include establishing clear pricing governance and processes, effective negotiation, and driving the necessary change management to ensure pricing discipline and strategic execution across all regions. 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 2026 Summer Intern - Process Engineering We advance science so that we all have more time with the people we love. Department Summary GenMark Diagnostics, a proud member of the Roche Group, is committed to delivering world-class solutions for multiplex testing, bolstering Roche's mission to advance the diagnosis of infectious diseases and combat antibiotic resistance. Automation Engineering is an integral part of the Manufacturing Technical Operation group in driving innovation and automation. We work alongside our operation partners to develop, characterize and optimize manufacturing process in a GMP environment. We are also responsible for designing and implementing automated manufacturing equipment to enhance production efficiency and quality. This internship position is located in CARLSBAD, on-site. The Opportunity Applications for the Summer 2026 Roche Summer Internship Program are now open! As a Process Engineering intern, you'll have the opportunity to gain valuable hands-on experience by contributing to multiple projects within the Automation Engineering team, from PCB biosensor processing to high-throughput consumable packaging. Furthermore, you will be expected to: Attend meetings, read independently on relevant topics, and perform tasks independently as appropriate. Assist in designing and implementing new equipment and tools to improve manufacturing efficiencies and improve quality. Utilization of data collection, management, analytics techniques to identify trends & actionable insights. Provide technical support and engineering solutions for process and equipment-related issues. Program Highlights Intensive 12-weeks, full-time (40 hours per week) paid internship. Program start dates are in May/June 2026 (Summer). 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) Required Education: You meet one of the following criteria: Must be pursuing a Bachelor's Degree (enrolled student). Must be pursuing a Master's Degree (enrolled student). Required Majors: Chemical Engineering, Bioengineering, Biomedical Engineering, or related field. Required Skills: Willingness to learn. Good time management. Strong communication and interpersonal skills. Preferred Knowledge, Skills, and Qualifications Please note: The goal of the internship is to expose you to the medical device industry & the myriad opportunities within it. The following skills will give you an idea of different assignment possibilities. You do NOT need to have all of these skills in order to apply. Not all internships will use all these skills. Experience with presentation software: Google Slides, Lucid Chart. Base knowledge of medical device manufacturing or process development. Base knowledge of data analysis (Excel or JMP). Base knowledge of technical writing. Base knowledge of CAD software (SolidWorks). Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of Carlsbad, California is $23.00-$35.00 per 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 GenMark is now a proud member of the Roche Group, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. As a global leader in healthcare, Roche Diagnostics offers a broad portfolio of products, tools and services that help in the prevention, diagnosis and management of diseases like HPV, HIV, hepatitis and diabetes as well as other medical conditions, such as fertility and blood coagulation. With the addition of GenMark to the Roche Group, syndromic infectious disease diagnostics is now added to the long list of disease states and conditions that the Roche Group addresses. GenMark's ePlex true sample-to-answer system offers unique solutions to address the most significant challenges facing clinical laboratories, while supporting hospital systems to deliver patient-centered, value-based care. ePlex streamlines the diagnostic workflow from physician order entry to the final test report and is the true sample-to-answer solution designed to improve patient care, reduce costs, and increase lab efficiency. GenMark is headquartered in Carlsbad, California. GenMark 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 Pharma Technical Operations (PT) department is establishing the One PT Data Office to serve as the strategic center for data governance, strategy, and enablement across the entire global PT network. This team is at the heart of our digital transformation, responsible for architecting and leading a central data office to unlock the full potential of PT's data assets. The Head of PT Data Acceleration will be accountable for establishing this critical function in close collaboration with the Head of PT Data Governance. This role is central to creating a single, unified data strategy that will serve as the backbone for our data driven decision making in PT as well for our digital transformation. You will be at the heart of our transformation, building a world-class data organization to unlock the full potential of PT's data assets. You will build and lead a high-performing team, champion a data-first culture across PT, and ensure that data is managed as a strategic asset to accelerate the realization of patient benefits. This pivotal role requires a visionary leader capable of building a unified data ecosystem, delivering measurable outcomes, and ensuring our data capabilities are a key driver of efficiency, quality, and innovation. **The Opportunity** + Provide strategic leadership and vision for data management across PT, ensuring alignment with PT's digital strategy and Roche's overall data ambitions. + Develop, champion, and execute a comprehensive, long-term data strategy and Data Product roadmap, identifying high-impact opportunities in close partnership with PTx business stakeholders to meet their organizational objectives. + Collaborate with the Head of Data Governance to establish and enforce a robust, centralized data governance framework, including policies, standards, and stewardship practices to ensure the quality, integrity, and security of data across the entire product lifecycle. + Accountable for breaking down data silos and architecting a single, unified data ecosystem for PT that is FAIR (Findable, Accessible, Interoperable, Reusable). + Drive the adoption of cutting-edge technologies and platforms to ensure state of the art data infrastructure, in close collaboration with IT and IT/OT teams. + Build, recruit, develop, and retain a world-class, globally distributed team of data professionals, nurturing their skills in data governance, strategy, and architecture. + Build and maintain strong strategic relationships with key senior stakeholders across PT (e.g., manufacturing, quality, supply chain, development, regulatory), global functions, and IT. + Serve as the ultimate steward of our data, ensuring all data activities are conducted in compliance with GxP, GDPR, and other relevant regulations, thereby building trust with all stakeholders. + Define, track, and report on the tangible business value, ROI, and key performance indicators of data initiatives to senior leadership. **Who You Are** + You have 15+ years of progressive experience in data management, governance, or strategy, with at least 10 years in a senior leadership role building and leading centralized data functions. + You have a deep understanding of the pharmaceutical or life sciences industry, including regulatory requirements like GxP environments and data integrity. + Demonstrated experience driving the implementation of enterprise-wide data strategies that deliver measurable business value, ideally in a manufacturing or technical operations context. + You possess expert-level knowledge of data governance frameworks, architecture principles, master data management, and modern cloud-based data platforms. + You are an exceptional strategic thinker with proven ability to translate complex business challenges into an actionable data strategy and roadmap. Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity! **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.

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 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.

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. The company has approved medicines that treat the underlying causes of multiple chronic, life-shortening genetic diseases - cystic fibrosis, pain, sickle cell disease and transfusion-dependent beta thalassemia - and continues to advance clinical and research programs in these diseases. Vertex also has a robust clinical pipeline of investigational therapies across a range of modalities in other serious diseases. The Principal Research Scientist will focus on targeted drug delivery including nucleic acid therapies. This role will be on-site in our state-of-the-art research site in San Diego. The successful candidate will have extensive expertise in receptor biology and targeted delivery in extrahepatic tissues/cells which is instrumental in the development of novel therapeutics. Key Duties and Responsibilities: Develop and implement strategic plans for receptor & ligand identification, characterization, optimization, and application in drug discovery. Responsible for executing research plans, collecting and interpreting data, trouble shooting, and defining next steps. Collaborate with cross-functional partners (medicinal chemistry, computational genomics, molecular and cellular biology, pharmacology, protein sciences) to support integrated drug discovery programs from target validation through lead optimization. Apply innovative approaches and stay current with advances in receptor biology, ligand discovery, and nucleic acid therapeutics to strengthen pipeline opportunities. Prepare and present data in project team meetings, contributing scientific insight and recommendations to guide program strategy. Maintain high standards of scientific rigor, accurate documentation, data integrity, and compliance with regulatory guidelines. Knowledge and Skills: Strong expertise in receptor biology, ligand-receptor interactions and signaling mechanisms. Hands-on experience with biochemical, biophysical, and/or cell-based assays to study receptor function and behavior. Experience with ligand-mediated delivery into specific tissues or cell types is highly desirable. Demonstrated track record of scientific achievement (e.g., publications, presentations, or contributions to therapeutic programs) in receptor biology and targeted drug delivery. Ability to collaborate effectively within multidisciplinary project teams. Excellent personal and communication skills, with the ability to influence stakeholders and drive decision-making across functions. Proven ability to thrive in a fast-paced, multidisciplinary, and innovative environment Education and Experience: Ph.D. (or equivalent degree) in biology, biochemistry or related science and 4-7 years of relevant post-doctoral employment experience, or Master's degree (or equivalent degree) in biology, biochemistry or related science and 7+ years of relevant employment experience, or Bachelor's Degree (or equivalent degree) in biology, biochemistry or related science and 10+ years of relevant employment experience #LI-KM1 #LI-Onsite Pay Range: $136,000 - $204,000 Disclosure Statement: The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more. Flex Designation: On-Site Designated Flex Eligibility Status: In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility. Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time. Company Information Vertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

Kickstart Your Career at Vertex! Are you ready to make a real impact? At Vertex, our mission is to tackle serious diseases and to change lives, for the better, for the future. Our aim is to give you the skills, insights, and career guidance to be an important part of that future; to turn your potential into progression. As a Vertex intern or co-op, you'll work on meaningful projects, collaborate with talented teams, and learn from industry leaders. We're passionate about innovation, inclusion, and supporting your growth-inside and outside the lab. Why Vertex? Real Projects: You'll work on assignments that make a real impact, not just busy work. Mentorship & Networking: Connect with leaders and peers who want to see you succeed through professional networks, connections, and collaborations that will shape your longer-term career. Flexible & Supportive: We offer flexible work options with Flex @ Vertex and prioritize your wellbeing. Inclusive Culture: Collaboration and inclusion are embedded in everything we do. Career Launchpad: Build skills, explore career paths, and get guidance for your future career. Ready to apply? Submit your application and let's turn possibilities into reality! Your Impact The Vertex Preclinical Formulation internship program is a multi-week experiential training program for students currently working towards an undergraduate or advanced degree in Pharmacy, Chemistry, Biochemistry, Chemical Engineering, Biochemical Engineering, or a related field of study. If you are passionate, collaborative, and growth-minded, an internship at Vertex will help you gain meaningful experience in our formulation functional areas and serve as a launchpad for your career. Important Notice Regarding Internship and Co-op Inquiries At Vertex Pharmaceuticals, we are committed to providing a fair and structured recruitment process for all students interested in internship and co-op opportunities. To ensure consistency and equity, all student applications must go through our Early Talent Acquisition Team. Due to the high volume of interest, we are unable to respond to individual solicitation. Direct solicitation to Vertex employees- including senior leaders via email will result in removal from the recruiting process. We appreciate your enthusiasm and interest in Vertex. To be considered for internship or co-op roles, please apply directly through our official application channels. (************************************************************************** Thank you for respecting our process and helping us maintain a fair experience for all candidates. What you will be doing: The Preclinical Formulation department located in San Diego, CA is responsible for serving the Chemistry team and preparing Vertex medicines for dosing. To execute this function, we run benchtop experiments to understand how the compounds may translate to animal models. The focus of this position is on automating one of these experiments using a liquid/solid handling robot. We are looking for an enthusiastic intern to learn the robot software, code the workflow, and execute the experiment in simulation/real. The project will conclude with a PowerPoint and/or poster presentation to the site on findings. Key responsibilities include: Learning the day-to-day experiments of preclinical formulation experimentation Running benchtop experiments using a wide variety of wet lab instruments including but not limited to pipettes, centrifuges, pH meters and analytical equipment Learning liquid/solid handling software and hardware Designing/coding liquid handling workflow What you will need to succeed: Enrolled in an undergraduate (Junior or Senior preferred but will consider underclass applicants with extensive experience) or graduate degree program and majoring in Pharmacy, Chemistry, Biochemistry, Chemical Engineering, Biochemical Engineering, Biomedical Engineering, or a related scientific field. Wet lab experience (pipetting, pH meter use, proper lab safety) Basic coding knowledge (logic, loops, variable understanding and function understanding) Excellent communication and presentation skills Legal authorization to work in the United States, now and in the future. Please note that Vertex does not provide sponsorship for internships or entry level roles within this part of the organization. You must be available to work full-time, 40 hours per week from May - August 2026 Program Details: Full-time, paid internship $20.00 - 32.00 USD/hour Program Dates: May - August 2026 At Vertex, we believe that when you feel your best, you can perform at your best. That's why our US benefits and global well-being resources are designed to support you. • Free 24/7 onsite gym access and free access to group exercise classes • Subsidized commuter benefits- transit and parking • Provided meals-free breakfast daily! • Career development opportunities and events, including C Suite engagement • Social events-both intern-only and company-wide • Location-specific perks and extras! • Recognition of National Intern Day Equal Opportunities Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Vertex is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. Accessibility & Accommodations We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Vertex is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com. Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant's ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role, Vertex is unable to sponsor non-U.S. persons to apply for an export control license. This job posting is for a temporary role with a third-party agency partner that provides services to Vertex. The individual selected for this role will be offered the role as an employee of that third-party agency; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency upon offer. For any questions or concerns, please contact early_*************** Pay Range: $0 - $0 Disclosure Statement: The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more. Flex Designation: Hybrid-Eligible Or On-Site Eligible Flex Eligibility Status: In this Hybrid-Eligible role, you can choose to be designated as: 1. Hybrid: work remotely up to two days per week; or select 2. On-Site: work five days per week on-site with ad hoc flexibility. Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time. #LI-Hybrid Company Information Vertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

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.

The Senior Director, Structural Biology and Biophysics will define and execute a forward-looking vision for structural biology and biophysics to accelerate drug discovery. This leader will further develop our research capabilities in structure-enabled discovery, driving scientific excellence, innovation, and integration across disciplines. Based at our state-of-the-art research site in San Diego, this individual will combine deep technical expertise with strategic foresight to position structural biology as a core differentiator in our discovery platform. KEY RESPONSIBILITIES Define and articulate a scientific vision and strategic plans that integrate experimental structural biology and biophysics data as well as computational approaches to accelerate drug discovery Lead and manage a team specialized in structural biology and biophysics. Provide guidance and mentorship. Foster a collaborative work environment. Champion existing and new structural biology and biophysical technologies that advance drug discovery projects forward. Propose new applications, apply technology, and follow up on new MoA, drug target and binding site identification and/or kinetic analysis of drug binding. Synthesize diverse approaches across modalities, build strategic collaborations within and outside the organization, and articulate how structural insights translate to biological and therapeutic impact. Independently perform hands-on experimental troubleshooting and methods development in biophysical assay development and protein structure determination by crystallography and/or CryoEM. Stay current with the latest advancements in the field of structural biology and biophysics, and integrate new technologies and methodologies into the drug discovery process. Propose and implement novel and improved data analysis tools. Maintain the excellence of standards for structure and interpretation of all laboratory records, electronic database entries, internal reports, patents, and external communications from the team. Ensure compliance with relevant regulatory guidelines, maintain accurate records, and promote a culture of scientific rigor and integrity within the team. Ensure effective interaction & communication between the structural biology and biophysics group and other disciplines within Research such as pharmacology, molecular and cellular biology, computational chemistry, etc. Develop and implement strategies in collaboration with key stakeholders to ensure the discovery and development of clinical candidates with high clinical success rates. Lead and/or contribute to cross-site and cross-functional goals within Vertex. Required Education Level Ph.D. (or equivalent degree) in Structural Biology, Biophysics, or a related field and 11+ years of industry / academic experience with a minimum of 5 years managing a team. Master's degree (or equivalent degree) and 15+ years of relevant employment experience, or Bachelor's Degree (or equivalent degree) and 20+ years of relevant employment experience. Extensive experience in pharmaceutical, biotechnology, or leading academic biomedical research setting, with a proven track record of leading and managing teams in structural biology and biophysics. Experience in applying structural biology and biophysics to advance drug discovery programs. Required Knowledge/Skills Established reputation with a strong track record of scientific impact in driving drug discovery programs forward by initiating and implementing structural biology and biophysics for mechanism-of-action studies and drug target or protein binding site identification and characterization. Experience can come from functional or cross-functional project leadership roles. Industry experience is preferred. Demonstrated ability to craft and communicate a unifying scientific vision that integrates structural biology, biophysics, and computation into discovery strategies. Proven success in applying structural insights to advance drug discovery from target validation through lead optimization. Experience with integral membrane proteins is highly desirable. Experience in managing scientific teams, individual and team performance, goal setting, and career growth development and building a culture of innovation and inclusion. Demonstrated independent thought/creativity in science, leadership skills, and ability to inspire and motivate drug discovery teams. Excellent communication (oral and written) in articulating goals, objectives and results to the group and larger cross-functional project teams. Strong inter-personal, oral, and written communication skills. Extensive experience interfacing with internal and external stakeholders to collaborate and execute on research programs, deliver results, and influence decision making. Ability to navigate and be successful in a fast-paced, innovative, and multi-disciplinary work environment. #LI-KM1 #LI-Onsite Pay Range: $221,900 - $332,800 Disclosure Statement: The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more. Flex Designation: On-Site Designated Flex Eligibility Status: In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility. Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time. Company Information Vertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com