Personalis jobs in Fremont, CA

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. Summary: A CLS Supervisor performs and reports on clinical laboratory testing that aids physicians in diagnosing and treating patients. A key part of the role is supervising team members and ensuring that all laboratory procedures are followed for specimen handling, next-generation sequencing (NGS) processes, test analyses, and the accurate maintenance of patient records. In our lab, we foster a positive, friendly, and team-based environment. We all pitch in to achieve our common goals and support each other. You'll work in a dynamic atmosphere, gaining hands-on experience at multiple benches, including extractions, library preparation, and sequencing. You'll also partner with our lab assistants to coordinate pre-analytical and post-analytical tasks. Available Shifts: Sun - Thu, 10:00pm - 6:30am Responsibilities: Perform and report clinical laboratory testing on patient samples to aid physicians diagnose and treat patients. This includes the following areas: Extractions Library Preparation Enrichments Sequencing Handle and process all patient specimens according to laboratory procedures, ensuring accurate and timely record-keeping and reporting of results. Select, implement, and evaluate quality control materials for statistical process control of laboratory assays. Troubleshoot assays and equipment when quality control materials fail to perform as expected. Document all corrective actions taken when test systems deviate from established performance specifications. Assist in audits by regulatory bodies like CAP and external customers. Participate in activities that support the laboratory's necessary licensure, including quality management and on-site inspections. Identify and correct problems that may negatively affect test performance or result reporting. If a problem cannot be immediately corrected, notify a supervisor, clinical consultant, or director. Train other CLS and lab personnel on laboratory methods. Monitor the activities of non-licensed staff. Provide guidance to team members on troubleshooting and deviation investigations. Assist in assay development activities. Demonstrate strong analytical skills and independent critical thinking. Apply technical and functional knowledge to help the team meet its goals. Work independently to identify and resolve complex, open-ended problems. Requirements: Education: Bachelor's degree, preferably in sciences or related discipline. Licensure: Valid California Clinical Laboratory Scientist (CLS) or Clinical Genetic Molecular Biologist Scientist (CGMBS) license. Experience: At least four years of CLS experience in a clinical laboratory environment. Minimum 1 year experience in a Lead role is required. Preferred Skills: Experience with manual DNA/RNA extractions, manual library preparation, and automated liquid handlers. The hiring range for this position is $72.10 to $81.70 per hour plus applicable shift differential. The offer will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. Our full-time regular positions also include an annual performance-based bonus (or a sales incentive plan) and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, dependent on the level and position offered. Personalis is an equal opportunity employer and is committed to the full inclusion of all individuals. As part of this commitment, Personalis will ensure that persons with disabilities are provided with reasonable accommodations. If you need an accommodation to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your recruiter know, if/when they contact you. Personalis offers a competitive compensation package and benefits including medical, dental, vision, 401(k) match, ESPP, tuition reimbursement, sick/vacation time, commuter benefits/ EV charging stations, onsite gym, and wellness benefits. (For US only, benefits in other countries may vary.) #LI-KK1 #LI-Onsite

Veracyte is seeking a Marketing Manager for the Prosigna Breast Cancer Assay, a genomic test designed to aid in treatment decisions for patients with breast cancer. The Marketing Manager will help drive global growth in Prosigna and breast cancer product portfolio by developing a multi-channel marketing plan, creating messaging, collateral and collaborating with field teams to enable sales growth. The ideal candidate will have experience with product marketing and brand development, gathering voice of customer feedback, product positioning, and digital marketing strategies. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Execute marketing operations for all aspects: Lead the development of the creation of global and US specific marketing materials Lead and support the development of content for digital marketing activities, including the website and social media, in collaboration with the corporate marketing team Lead conference planning and execution in collaboration with the corporate marketing team Budget management Closely partner with sales to: Develop and ensure that breast cancer messaging, sales tools, and other collateral are continuously relevant and accurate Create new marketing collateral and sales training, as needed Consistently keep a pulse on the latest market developments and proactively refine strategy, selling direction and tactics as necessary Distill customer feedback into actionable and appropriate marketing-related solutions Execute assigned aspects of the ongoing commercial initiatives to drive significant revenue growth Conduct qualitative and quantitative voice of customer research, market assessment, competitive analysis, as necessary to support product sales growth and product improvement Build relationships with key physicians to build domain expertise and strategic insights Who You Are: You are a highly motivated, results-driven individual with entrepreneurial drive and a track record of success in marketing. You have a deep sense of accountability and desire to own the product, from crafting the strategy to rolling up your sleeves and executing the tactics. Additional Qualifications Include: Bachelor's degree in science required 5+ years combined experience in marketing/sales preferred Experience with LDT and IVD marketing Experience working cross-functionally Excellent attention to detail required Excellent presentation, written, verbal communication, and interpersonal skills Excellent analytical and technical skills Adaptability to changes and challenges Tenacity and the drive to make an impact Team player with demonstrated track record of collaboration with others Location: This role can be remote in the US. Minimum of 25% travel is expected. Travel to the San Diego, San Francisco and European home offices along with US and EU customer visits and conference attendance is expected #LI-Remote, #LI-Hybrid

The Clinical Data Manager is responsible for participating all aspects of Clinical Data Management Operations at Veracyte, ensuring data integrity and quality for clinical studies. This is a hands-on role that requires technical expertise in the complete data management lifecycle. This is a remote role, with a strong preference for someone in San Diego, CA or San Francisco, CA Key Responsibilities: Support end-to-end clinical data management operations, from protocol design to database closure Support the implementation of comprehensive data management plans, validation specifications, and quality control procedures Participate in the design and validation of eCRF systems and edit checks aligned with protocol requirements Support database development, validation programming, and query management Collaborate with Clinical Affairs, Data Analysis, and IT teams to establish data collection methods and quality standards Generate key metrics reports and data analytics for clinical studies. Who You Are: Bachelor's degree in Computer Science, Life Sciences, or related field 4+ years hands-on experience in IVD, Medical Device, or Pharmaceutical clinical data management Knowledge of GCP and GCDMP and proficiency in the following: Programming languages (R, SAS) Database management (SQL, PL/SQL) EDC systems and clinical data management platforms (e.g. Medidata, Medrio) CTMS and eTMF platforms with strong preference for experience with Veeva Vault Sample management platforms (e.g. LabVantage) Microsoft Office Suite Technical Expertise: CDISC/CDASH/SDTM/ADAM standards FDA guidelines and regulations Database validation and quality control processes Clinical trials Experience with Medidata Experience with Veeva Vault Experience with LabVantage Clinical trial data workflows Teamwork and collaboration Competencies: Excellence in within and cross-functional team collaboration Clear communication of technical concepts to non-technical stakeholders Proactive issue identification and resolution Ability to work independently while maintaining team alignment Impact: This role directly contributes to improving patient outcomes by ensuring the highest quality clinical data management standards in diagnostic testing development and validation. #LI-Remote

What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. The Onsite Field Service Engineer will provide daily on-site support performing installation, upgrade, diagnoses, troubleshooting, and repair of complex equipment and systems. Provides feedback to Manager and identifies opportunities to promote efficiency in day to day operations. The successful applicant will be part of an award-winning customer support team that leads the industry in customer satisfaction. Delivers technical support to onsite sites utilizing experience performing installations, diagnoses, troubleshooting, service, and repair of complex Illumina instrumentation and systems. This role requires troubleshooting, communication, time management, situational awareness, poise under pressure, and collaboration. You will be expected to build and maintain strong relationships across in-district Service and Support teams. Responsibilities: * Proficient at installation, repair and maintenance of Illumina platforms * Troubleshoot a wide variety of complex customer reported problems * Proactively monitor, schedule, and prioritize tasks to maximize instrument uptime and customer satisfaction * Responsible for completing post repair/install validation runs as required on all platforms * Manage all administrative tasks (SFDC case management) in a quality manner and within the established guidelines, making suggestions and changes when needed * Independently manage account, build and help strengthen customer relationships * Schedule and perform equipment upgrades and new installations * Utilize and maintain up to date Service and training manuals, Field Service Bulletins, SOPs and facilitate remote connectivity to customer instrumentation. * Responsible for escalating repairs as needed and primary point of contact for escalation related activities * Running reports on instrument failures and using data to proactively service instruments in order to avoid costly downtime * Lead regular meetings with site personal reporting out metrics related to instrument performance, downtime etc. * Partner with NSST and product support for any ongoing sustaining engineering activities (product performance monitoring or product improvement efforts) * Responsible for communicating and overseeing any rotational support locally or from other regions * Resource to assist other SSE's in troubleshooting complex issues * Provide additional onsite training/support to other SSE's to further develop their skill sets * Identify opportunities for gaining site efficiencies which will promote a decrease in mean time between repair and increase instrument uptime * Ensure proper inventory levels of service parts and make changes as needed All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities. Requirements: * BS in Electrical/Electronic Engineering, Biomedical Engineering, Mechanical Engineering, Bioengineering, related degree with knowledge in the biotechnology/biomedical industry, or applicable experience * 2-6 years relevant experience or direct experience servicing our products * Must be highly motivated and have problem-solving ability * Ability to operate as an independent contributor and as a cooperative member of a team * Excellent verbal and written communications skills * Biotechnology/Biomedical industry knowledge, or applicable military experience * Demonstrated experience using electronic troubleshooting equipment; e.g. DVM, Oscilloscope, etc * Familiarity with field optical alignments, robotics, electrical/electronics, and mechanical systems * Technical knowledge of computer hardware, Windows OS, and networking * Planning, scheduling, and prioritization skills The estimated base salary range for the Onsite Field Service Engineer role based in the United States of America is: $70,800 - $106,200. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual's qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off. We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact accommodations@illumina.com. To learn more, visit: ****************************************************************** The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. We are always looking for great people to join our growing teams. If you don't see the right role posted but think we should meet you anyway, apply and let us know how you'd like to help! If we open a role that matches your experience, our team will reach out. ** Please note, while we do try to respond to all applicants who apply through our careers page, applications through this specific link may not receive a response. If there is a specific job you're interested in, please apply directly to that role. ** Personalis is an equal opportunity employer and is committed to the full inclusion of all individuals. As part of this commitment, Personalis will ensure that persons with disabilities are provided with reasonable accommodations. If you need an accommodation to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your recruiter know. Personalis offers a competitive compensation package and benefits including medical, dental, vision, 401(k) match, ESPP, tuition reimbursement, sick/vacation time, commuter benefits/ EV charging stations, onsite gym, and wellness benefits. (For US only, benefits in other countries may vary.) #LI-DNI

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. Summary: Under the direction of the department supervisor, technical/clinical consultant, and laboratory director, the Histotechnician will be responsible for processing FFPE specimens for microscopic evaluation to support our molecular diagnostics test offerings. Onsite: Tuesday-Saturday, 12 pm-8:30 pm Responsibilities: Perform sectioning of tissue using a microtome and mounting on glass slides Perform routine staining of tissue sections with automated and/or manual staining techniques Perform automated and/or manual coverslipping of slides Generate digital slide images for pathologist examination Perform manual and automated macrodissection Operate and perform instrument maintenance Perform histology lab functions while following laboratory safety and quality policies Comply with standard laboratory operating policies and procedures Use of good documentation practices to record specimen data manually or in Laboratory Information Management Systems Help meet TAT goals while maintaining high-quality productivity Maintain clean and organized work areas within the laboratory Report problems to the department supervisor/manager to ensure timely resolution Requirements: Associate's degree in chemical/physical/biological science or completion of a NAACLS-accredited Histotechnology program; Bachelor's degree in a laboratory science curriculum preferred 0-3 years experience working in a high-volume histology laboratory performing microtomy of various tissue types, H&E staining, and tissue embedding HT or HTL certification from ASCP required Experience working in IHC and digital imaging, tissue/tumor identification, and proficiency in reading pathology reports, a plus Excellent attention to detail, organization, and time management skills Ability to communicate effectively with excellent interpersonal skills Physical demands include stooping, turning, bending, squatting, kneeling, and the ability to lift up to 25 lbs. The hiring range for this position is $36.00 to $48.00 per hour, which may factor in various geographic regions. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. Our full-time regular positions also include an annual performance-based bonus (or a sales incentive plan) and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, dependent on the level and position offered. Personalis is an equal opportunity employer and is committed to the full inclusion of all individuals. As part of this commitment, Personalis will ensure that persons with disabilities are provided with reasonable accommodations. If you need an accommodation to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your recruiter know, if/when they contact you. Personalis offers a competitive compensation package and benefits including medical, dental, vision, 401(k) match, ESPP, tuition reimbursement, sick/vacation time, commuter benefits/ EV charging stations, onsite gym, and wellness benefits. (For US only, benefits in other countries may vary.) #LI-KK1 #LI-Onsite

PacBio (NASDAQ: PACB) is a premier life science technology company that designs, develops, and manufactures advanced sequencing solutions to help scientists and clinical researchers resolve genetically complex problems. Our mission is to enable the promise of genomics to better human health. Genomics is core to all biological processes, and our advanced genomics tools provide scientists and clinical researchers the insights to better understand biology and health. We are now entering the century of biology and genomics is at the heart of the next revolution. Become part of the new paradigm in gene sequencing and help shape the future of genomic study by joining the PacBio team. Position Summary: The Instrument Engineering team is seeking a highly motivated and detail-oriented NPI Mechanical Engineer II to support new product introduction (NPI), production, and product ramp-up activities. In this role, you will help bridge the transition from design to manufacturing, ensuring new instrument products are introduced efficiently, cost-effectively, and to the highest quality standards. You will work closely with R&D, Manufacturing, Quality, Supply Chain, and Contract Manufacturing partners to define processes, resolve technical challenges, and continuously improve product performance and manufacturability. This position offers the opportunity to work on complex, high-impact instrumentation that advances PacBio's mission of enabling the promise of genomics. Responsibilities: * Lead and execute NPI activities to ensure seamless product transitions from R&D to full-scale manufacturing. * Support instrument and sub-assembly builds, troubleshooting, and root cause analysis to improve yield and reliability. * Create, review, and release detailed engineering drawings, specifications, and BOM structures. * Design, validate, and document packaging for instruments and spare parts to meet quality and compliance standards. * Develop and implement scalable manufacturing processes and process control documentation. * Collaborate with Contract Manufacturing partners on training, issue resolution, and ongoing quality improvements. * Drive mechanical design, prototyping, integration, testing, and final product release activities. Required Qualifications: * Bachelor's degree in Mechanical Engineering. * A minimum of 4-6 years of relevant industry experience in mechanical design, manufacturing engineering, or new product introduction. * Proven hands-on experience in equipment assembly and/or hardware repair. * Ability to work independently with minimal supervision. * Excellent interpersonal, written, and verbal communication skills. * Excellent documentation skills with attention to detail and quality. * Results-driven mindset with a demonstrated desire to grow into roles with greater responsibility. This role is required to be onsite Monday-Friday. Candidates must have current authorization to work in the United States without the need for present or future sponsorship. You may be required from time to time to visit and work at PacBio locations and for such times as the Company considers necessary for the proper performance of your duties. All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, or on the basis of disability, gender identity, and sexual orientation. * #LI-Onsite Salary Range: $97,400.00 - $146,200.00 To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at PacBio. Staffing and recruiting agencies and individuals being represented by an agency are not authorized to use this site or to submit profiles, applications or resumes, and any such submissions will be considered unsolicited. PacBio does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to our jobs alias, PacBio employees or any other company location. PacBio is not responsible for any fees related to unsolicited resumes/applications. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, or on the basis of disability, gender identity, and sexual orientation. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact us at ************, or ****************************** for assistance. Visit our following pages for more information on: * FAQs * Benefits * Culture * Equal Opportunity Employment

. On-site cube available in South San Francisco or San Diego. We are seeking a talented and experienced data scientist to join our Data Analysis Team (DAT), as part of the R&D group for Veracyte Inc. This position offers a unique opportunity to work with experienced professionals to carry out AI/ML modelling and analysis of the world's largest database of cancer patients, encompassing multi-platform digital pathology, genomic and clinical outcome data. The primary objective of this role is to analysis millions of records of real-world insurance claims and EHR data to define clinical treatments and outcomes. The successful candidate needs to be proficient in state-of-art data extraction, transformation and loading (ETL), and statistical analysis to convert data into meaningful insights and stories. The candidate will also need to communicate and understand business needs, identify relevant data, process and analyze data accordingly. Experience of academic writing and prepare data/figures for manuscript are necessary for success in this position. The candidate should also be able to design graphics to explain AI models with known clinical or genomic features. Strong track record of publishing in both clinical and technical peer-review journals or conferences is highly desired. The ideal candidate is passionate about data, eager to learn independently, and possesses strong analytical, problem-solving, and storytelling skills. KEY RESPONSIBILITIES: Assist in analyzing real-world data to identify patterns for various clinical and business cases, including treatment patterns and management costs. Participate in Identifying key clinical events, such as cancer progression and treatments, using CPT, NDC, ICD codes, and structured database free text. Assist in conducting statistical analysis and survival modelling for the clinical events defined from real-world data. Ability to visualize finding from the data and summarize them in a coherent story. Support data scientists in developing digital pathology AI models Work with bioinformatician, statistician, and medical experts in manuscripts. Who You Are: REQUIRED EXPERIENCE: PhD in Statistics, Data Science, or equivalent field. 3+ years of experience of data/applied scientist role or equivalent. Experience in working with real-world data of insurance claims and EHR records Proficient in SQL and R. Strong skills with data clean-up, manipulation and visualization using tidyverse, ggplot in R or equivalent. Proficient in statistical analysis, especially in survival modelling and hypothesis testing (i.e., multivariate regression modelling with interaction effects). Experience working in cloud computing environments (AWS preferred). Demonstrated proficiency in summarizing and communicating findings from data, including an attention to detail when sharing findings. Ability to work effectively in a fast-paced and collaborative environment. Eagerness to learn new technologies and adapt to evolving requirements. RELEVANT EXPERIENCE (preferred but not required): Experience with cloud platforms (e.g., AWS, Azure, Google Cloud Platform) is desirable. Knowledge of basic bioinformatics, genomics, and cancer biology Past research experience in urological oncology, bioinformatics, digital pathology, or relevant fields Research experience with developing AI models such as LLM, vision/time series foundation models. #LI-Hybrid, or #LI-Remote

What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. Position Summary: This position is responsible for Quality activities that improve, monitor and measure Illumina's compliance with the Quality System Regulations, Illumina Quality policies, FDA regulations and ISO standards as well as Illumina product quality for current operation and compliance objectives. Responsibilities: * Lead or provide support to investigations to determine root causes on material quality issues and initiate/ensure corrective and preventive action plans are developed and executed. * Interface with Suppliers/CM (Contract Manufacturer), Engineering/ Manufacturing/ Quality Assurance/ Procurement departments to drive for quality improvements, specifically on incoming rejects, workmanship defects and primitive failures. * Drive Quality review with supplier/CM for improvement to meet quality expectation. * Constantly review quality processes and suggests improvements that can be implemented to improve performances. * Manage Supplier/CM through continuous improvement activities. * Compile and evaluate supplier/CM quality performance metrics. * Ensure that supplier's preventive and corrective action is implemented and effective * Provide monthly quality data/input for suppliers/CM's Scorecard. * Responsible for the qualification processes for suppliers, including new supplier evaluation, audit programs and supplier approval programs * Work closely with Procurement and Engineering departments to identify new suppliers for evaluation. * May be involved in providing training. * Other such duties that may be determined by Management Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs. Requirements: * Experience in managing Contract Manufacturer/Suppliers * Experience in conducting supplier audits. * Good understanding of FDA regulatory environment (CFR 820), 501k and ISO 13485 strongly preferred. * Experience in medical device/ pharmaceutical/ IVD is preferred. * Developing basic knowledge of FDA Quality System Regulations and/ or ISO 13485 Standard. * Developing basic knowledge of quality tools. * Beginning to intermediate experience with words processing and spreadsheets, charting, graphing tools and presentation tools. * May have experience with electronic production life (PLM), enterprise resource planning tools (SAP) and etc. * May have experience with statistical analysis packages, eg, JMP, minitab. * Must be detailed oriented, well organized and able to work independently and in teams. All listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities. Experience/Education: * Typically requires B.S. degree and 0 to 2 years of experience, or additional experience in lieu of degree. The estimated base salary range for the Supplier Quality Engineer role based in the United States of America is: $70,800 - $106,200. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual's qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off. We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact accommodations@illumina.com. To learn more, visit: ****************************************************************** The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.

Associate Director, Sales (West Region) The Associate Director, Sales (West Region) will lead PacBio's commercial efforts across the Western U.S., driving growth, expanding market presence, and leading a team of Territory Account Managers and Genomic Sequencing Specialists to exceed revenue and strategic objectives. This role reports directly to the Vice President of Global Sales and is a key member of the AMR leadership team. The ideal candidate is a dynamic commercial leader with a proven track record of sales excellence, strategic account growth, and people development. You will play a critical role in shaping territory and account plans, building high-performing teams, and driving collaboration across marketing, support, and product functions to deliver sustainable success. Key Responsibilities Lead, coach, and develop the West Region commercial team to achieve revenue, growth, and strategic objectives. Build and execute comprehensive regional business plans aligned with corporate priorities and customer needs. Directly manage and support key strategic and enterprise accounts to drive long-term partnerships and revenue expansion. Foster a culture of accountability, collaboration, and continuous improvement across the team. Partner with Strategic Marketing, Product Marketing, and Customer Support to optimize customer engagement and solution delivery. Provide accurate, data-driven forecasting and pipeline management within our current forecasting tools. Act as a visible and accessible leader - spending time in the field with customers and team members to identify opportunities and remove barriers. Collaborate with global and cross-functional counterparts to ensure alignment across multinational and strategic accounts. Represent PacBio at key conferences, customer meetings, and industry events, serving as a trusted ambassador for the company and its mission. Qualifications & Requirements Minimum 5 years of sales leadership experience, including at least 2 years at the Senior Manager level or equivalent senior management capacity. Bachelor's degree required, advanced degree preferred. Strong scientific or technical background. Demonstrated success managing teams selling high-end capital equipment and consumables in the Life Science and Clinical and Academic markets. Deep understanding of complex, high-value purchasing processes across multi-site organizations. Strong strategic and analytical mindset, with proven ability to translate strategy into actionable sales execution. Track record of developing talent and building high-performing commercial teams. Exceptional communication and presentation skills, with the ability to influence C-level stakeholders. Excellent interpersonal skills. Self-motivated, adaptable, and capable of thriving in a fast-paced, evolving environment. Willingness and ability to travel a minimum of 60%. Candidates must have current authorization to work in the United States without the need for present or future sponsorship. You may be required from time to time to visit and work at PacBio locations and for such times as the Company considers necessary for the proper performance of your duties. All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, or on the basis of disability, gender identity, and sexual orientation. #LI-Onsite Salary Range: $170,400.00 - $293,900.00 To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at PacBio. Staffing and recruiting agencies and individuals being represented by an agency are not authorized to use this site or to submit profiles, applications or resumes, and any such submissions will be considered unsolicited. PacBio does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to our jobs alias, PacBio employees or any other company location. PacBio is not responsible for any fees related to unsolicited resumes/applications. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, or on the basis of disability, gender identity, and sexual orientation. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact us at ************, or ****************************** for assistance. Visit our following pages for more information on: FAQs Benefits Culture Equal Opportunity Employment

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. Summary: In our lab, we foster a positive, friendly and team-based environment where we all pitch in to help achieve our common goals and support each other. We offer a dynamic atmosphere where you will have the opportunity to work on multiple benches such as extractions, Library prep, and sequencing. You will also partner with our lab assistants and coordinate with them on pre-analytical & post analytical tasks. Our Clinical Lab Scientists perform and report clinical lab testing on samples used by physicians in the diagnostic and treatment of patients. This will entail following the laboratory's procedures for specimen handling and next generation sequencing processes, test analyses, reporting and maintaining records of patient test results. Current opening: PM Shift Thursday to Monday (2pm to 10:30pm - Training schedule may be different) Days Onsite: Thursday - Monday Responsibilities: Maintain updated understanding and knowledge of the methods employed in the lab and the use of the resulting information by physicians through continuing education activities Supervise the activities of the lab in the absence of an onsite manager Identify problems that may adversely affect test performance or reporting of test results and either correct the problems or notify management Participate in activities which support all necessary licensure for the clinical laboratory, including quality management functions and on-site inspections of the laboratory Trains other CLS personnel and other staff in laboratory methods. Monitor the activities of non-licensed personnel as needed Follow the laboratory's established policies and procedures, quality control policies and activities including required documentation necessary to ensure compliance May be required to assist in assay development activities Other duties as required Requirements: Bachelor's degree, preferably in sciences or related disciplines California Clinical Laboratory Scientist license OR CGMBS license 0-4 years of experience in a clinical laboratory setting Beneficial to have experience with manual DNA/RNA extractions, manual library prep and working with a microtome The hiring range for this position is $56.25 to $62.00 per hour, which may factor in various geographic regions. The 3rd shift would be eligible for an additional shift premium. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. Our full-time regular positions also include an annual performance-based bonus (or a sales incentive plan) and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, dependent on the level and position offered. Personalis is an equal opportunity employer and is committed to the full inclusion of all individuals. As part of this commitment, Personalis will ensure that persons with disabilities are provided with reasonable accommodations. If you need an accommodation to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your recruiter know. Personalis offers a competitive compensation package and benefits including medical, dental, vision, 401(k) match, ESPP, tuition reimbursement, sick/vacation time, commuter benefits/ EV charging stations, onsite gym, and wellness benefits. (For US only, benefits in other countries may vary.) #LI-KK1 #LI-Onsite

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way - it's about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together: We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other The Position: Veracyte is seeking a highly motivated and experienced Senior Automation Engineer to join our growing Automation and Process Engineering team. This is a dynamic and impactful role where you will lead the development, optimization, and validation of automated liquid handling workflows-particularly using Hamilton platforms-for the implementation of molecular Laboratory Developed Tests (LDTs) in a regulated clinical laboratory environment. You will collaborate cross-functionally with R&D, Clinical Operations, Software, and IT teams to design and deploy innovative automation solutions that improve throughput, reproducibility, and efficiency. This is a unique opportunity to shape the future of molecular diagnostics through cutting-edge automation and process innovation. This is an onsite position based in our South San Francisco office. Responsibilities Design, program, and validate automated workflows for molecular assays using liquid handling platforms (eg. Hamilton) and other automated laboratory instruments Translate manual molecular protocols (e.g., RNA/DNA extraction, NGS library prep) into robust, high-throughput automated methods. Collaborate with Product Development, Clinical Operations, and Software teams to integrate automation with LIMS, bioinformatics pipelines, and data management systems. Lead portions or entire cross-functional projects from concept through implementation, ensuring timelines and deliverables are met. Collaborate with Equipment Engineering and Operations and QA on equipment qualification (IQ/OQ/PQ), calibration, and preventive maintenance procedures. Contribute to the development of custom 3D printed parts, software scripts, workcells, and novel automation technologies. Document workflows, SOPs, ERDs, and process maps in accordance with quality and regulatory standards. Provide technical mentorship and collaborate with internal stakeholders and external vendors. Who You Are: You've worked with both manual and automated molecular assays and feel right at home programming Hamilton systems. You might also have experience with microarray prep, NGS library prep, or RNA/DNA extraction from sample types like FFPE, blood, or cultured cells-that's a big plus. You know how to build automation workflows that work in a high-throughput, CLIA-regulated lab-not just in theory. You're good at spotting potential issues before they become problems, and you're the kind of person who enjoys figuring out how to fix things when they don't go as planned. You manage your time well, stay organized, and aren't afraid to try new approaches or take calculated risks. You enjoy working with others, sharing ideas, and solving tough problems as a team. Most of all, you're excited about using your skills to help push the boundaries of what's possible in molecular diagnostics. Required Qualifications Bachelor's degree in Life Sciences, Engineering, or related field. Minimum 5-7 years of industry experience in laboratory automation, with deep expertise in Hamilton Robotics platforms (preferred). Strong background in molecular biology techniques such as PCR, RNA/DNA extraction, microarray, and NGS. Proven experience designing, programming, and troubleshooting automated workflows in a clinical or regulated lab. Familiarity with CLIA, CAP, GxP, and 21 CFR Part 11 compliance. Excellent organizational, communication, and documentation skills. Ability to work independently and collaboratively across multidisciplinary teams. Proficiency in MS Office (Word, Excel, PowerPoint). Preferred Qualifications Experience with scripting languages (e.g., Python, C#) and database integration. Familiarity with Agile/Scrum methodologies and tools like Jira and Confluence. Experience with CAD design and 3D printing. Proficiency with Microsoft Power Platform and modern AI tools. Experience integrating automation with cloud-based data systems and bioinformatics pipelines. #LI-Onsite The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Pay range$135,000-$175,000 USDWhat We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. About Veracyte Veracyte (Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit **************** or follow us on LinkedIn or X (Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to ********************

Title: Senior Technician Engineer, Systems Integration PacBio (NASDAQ: PACB) is a premier life science technology company that designs, develops, and manufactures advanced sequencing solutions to help scientists and clinical researchers resolve genetically complex problems. Our mission is to enable the promise of genomics to better human health. Genomics is core to all biological processes, and our advanced genomics tools provide scientists and clinical researchers the insights to better understand biology and health. We are now entering the century of biology and genomics is at the heart of the next revolution. Become part of the new paradigm in gene sequencing and help shape the future of genomic study by joining the PacBio team. Pacific Biosciences is seeking a hands-on Engineering Technician to join our Systems Integration team. This person will be responsible for supporting an instrument sequencing lab as well as the development of next-generation SMRT sequencing platforms. The person will work hand in hand with Mechanical, Electrical, Optical, Systems and Manufacturing Engineering teams in all phases of a product release. Responsibilities: * Serve as the first line of contact for instrument issues and complaints. * Performing routine instrument maintenance and repairs. * PCBA soldering, rework, and cabling. * Building test fixtures and executing necessary tests. * Supporting prototype instrument builds and troubleshooting. * Identifying issues and communicating feedback to development teams. Required Qualifications: * A minimum of 3-5 years engineering technician experience. * Experience in a ISO/cGMP production environment. * Strong experience with PCBA soldering, rework, and cabling. * High School diploma or GED equivalent. * Strong analytical and problem-solving skills. * Strong attention to detail. * Effective interpersonal skills. * Proficient with Microsoft Word, Excel and work-order type transactions. * Excellent interpersonal, written, and verbal communication skills. Preferred Experience: * Experience building test fixtures and executing tests. Candidates must have current authorization to work in the United States without the need for present or future sponsorship. This role is 100% onsite. You may be required from time to time to visit and work at PacBio locations and for such times as the Company considers necessary for the proper performance of your duties. All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, or on the basis of disability, gender identity, and sexual orientation. #LI-Onsite Salary Range: $77,700.00 - $116,500.00 To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at PacBio. Staffing and recruiting agencies and individuals being represented by an agency are not authorized to use this site or to submit profiles, applications or resumes, and any such submissions will be considered unsolicited. PacBio does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to our jobs alias, PacBio employees or any other company location. PacBio is not responsible for any fees related to unsolicited resumes/applications. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, or on the basis of disability, gender identity, and sexual orientation. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact us at ************, or ****************************** for assistance. Visit our following pages for more information on: * FAQs * Benefits * Culture * Equal Opportunity Employment

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. Days onsite: Sunday-Thursday, 10:00pm-6:30 am Training hours may be at different shifts. Responsibilities: Perform nucleic acid extraction from various sample types in a Biosafety Level 2 laboratory (e.g., FFPE, blood, plasma, and more) Quantify extracted materials by following QC protocols Prepare extracted materials for library prep using automated and manual procedures. Record sample processing workflows in real-time through a Laboratory Information Management System (LIMS) Maintain robotic liquid handlers and other instruments for optimal performance Assists in data transfer and basic QC evaluation of data Perform troubleshooting and system evaluations when necessary, in communication with the automation support team, laboratory supervisor, and/or third-party technical support teams Escalates issues to a supervisor when problems arise with sample processing Maintain appropriate supplies and equipment to maximize department efficiency and meet established budgetary and quality goals Support and ensure compliance with the laboratory's quality control procedures and policies Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications Demonstrate knowledge of laboratory safety protocols Demonstrate commitment to quality and continuous improvement Use effective two-way communication and participate in general laboratory meetings Perform other duties as assigned, including performing workflows outside of extractions Requirements: BA/BS in a biological discipline 0-2 years of relevant laboratory experience Familiarity with Hamilton, or other robotic liquid handlers, is desired Familiarity with LIMS or sample management tracking systems is desired Familiarity with Quality control of samples and quantification devices (e.g., TapeStation, Qubit, qPCR) Flexible and adaptive in a frequently changing environment Strong communication skills, ensuring effective communication when issues arise. Strong organizational skills and attention to detail Ability to analyze and solve basic problems Ability to work as part of a team in a highly collaborative environment Ability to work independently with minimal supervision Desire to learn new skills and grow his/her knowledge of next-generation sequencing technologies Strong desire to work in a demanding, high-energy, hands-on environment The hiring range for this position is $27.50 to $34.60 per hour, which may factor in various geographic regions. This shift is eligible for an additional shift premium. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. Our full-time regular positions also include an annual performance-based bonus (or a sales incentive plan) and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, dependent on the level and position offered. Personalis is an equal opportunity employer and is committed to the full inclusion of all individuals. As part of this commitment, Personalis will ensure that persons with disabilities are provided with reasonable accommodations. If you need an accommodation to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your recruiter know, if/when they contacts you. Personalis is an Equal Opportunity Employer/Minorities/Females/Veterans/Disabilities. Personalis offers a competitive compensation package and benefits including medical, dental, vision, 401(k) match, ESPP, tuition reimbursement, sick/vacation time, commuter benefits/ EV charging stations, onsite gym, and wellness benefits. (For US only, benefits in other countries may vary.) #LI-KK1 #LI-Onsite

What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. The Onsite Field Service Engineer will provide daily on-site support performing installation, upgrade, diagnoses, troubleshooting, and repair of complex equipment and systems. Provides feedback to Manager and identifies opportunities to promote efficiency in day to day operations. The successful applicant will be part of an award-winning customer support team that leads the industry in customer satisfaction. Delivers technical support to onsite sites utilizing experience performing installations, diagnoses, troubleshooting, service, and repair of complex Illumina instrumentation and systems. This role requires troubleshooting, communication, time management, situational awareness, poise under pressure, and collaboration. You will be expected to build and maintain strong relationships across in-district Service and Support teams. Responsibilities: * Proficient at installation, repair and maintenance of Illumina platforms * Troubleshoot a wide variety of complex customer reported problems * Proactively monitor, schedule, and prioritize tasks to maximize instrument uptime and customer satisfaction * Responsible for completing post repair/install validation runs as required on all platforms * Manage all administrative tasks (SFDC case management) in a quality manner and within the established guidelines, making suggestions and changes when needed * Independently manage account, build and help strengthen customer relationships * Schedule and perform equipment upgrades and new installations * Utilize and maintain up to date Service and training manuals, Field Service Bulletins, SOPs and facilitate remote connectivity to customer instrumentation. * Responsible for escalating repairs as needed and primary point of contact for escalation related activities * Running reports on instrument failures and using data to proactively service instruments in order to avoid costly downtime * Lead regular meetings with site personal reporting out metrics related to instrument performance, downtime etc. * Partner with NSST and product support for any ongoing sustaining engineering activities (product performance monitoring or product improvement efforts) * Responsible for communicating and overseeing any rotational support locally or from other regions * Resource to assist other SSE's in troubleshooting complex issues * Provide additional onsite training/support to other SSE's to further develop their skill sets * Identify opportunities for gaining site efficiencies which will promote a decrease in mean time between repair and increase instrument uptime * Ensure proper inventory levels of service parts and make changes as needed All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities. Requirements: * BS in Electrical/Electronic Engineering, Biomedical Engineering, Mechanical Engineering, Bioengineering, related degree with knowledge in the biotechnology/biomedical industry, or applicable experience * 2-6 years relevant experience or direct experience servicing our products * Must be highly motivated and have problem-solving ability * Ability to operate as an independent contributor and as a cooperative member of a team * Excellent verbal and written communications skills * Biotechnology/Biomedical industry knowledge, or applicable military experience * Demonstrated experience using electronic troubleshooting equipment; e.g. DVM, Oscilloscope, etc * Familiarity with field optical alignments, robotics, electrical/electronics, and mechanical systems * Technical knowledge of computer hardware, Windows OS, and networking * Planning, scheduling, and prioritization skills The estimated base salary range for the Onsite Field Service Engineer role based in the United States of America is: $70,800 - $106,200. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual's qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off. We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact accommodations@illumina.com. To learn more, visit: ****************************************************************** The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.

PacBio (NASDAQ: PACB) is a premier life science technology company that designs, develops, and manufactures advanced sequencing solutions to help scientists and clinical researchers resolve genetically complex problems. Our mission is to enable the promise of genomics to better human health. Genomics is core to all biological processes, and our advanced genomics tools provide scientists and clinical researchers the insights to better understand biology and health. We are now entering the century of biology and genomics is at the heart of the next revolution. Become part of the new paradigm in gene sequencing and help shape the future of genomic study by joining the PacBio team. Position Summary: The Instrument Engineering team is seeking a highly motivated and detail-oriented NPI Mechanical Engineer II to support new product introduction (NPI), production, and product ramp-up activities. In this role, you will help bridge the transition from design to manufacturing, ensuring new instrument products are introduced efficiently, cost-effectively, and to the highest quality standards. You will work closely with R&D, Manufacturing, Quality, Supply Chain, and Contract Manufacturing partners to define processes, resolve technical challenges, and continuously improve product performance and manufacturability. This position offers the opportunity to work on complex, high-impact instrumentation that advances PacBio's mission of enabling the promise of genomics. Responsibilities: Lead and execute NPI activities to ensure seamless product transitions from R&D to full-scale manufacturing. Support instrument and sub-assembly builds, troubleshooting, and root cause analysis to improve yield and reliability. Create, review, and release detailed engineering drawings, specifications, and BOM structures. Design, validate, and document packaging for instruments and spare parts to meet quality and compliance standards. Develop and implement scalable manufacturing processes and process control documentation. Collaborate with Contract Manufacturing partners on training, issue resolution, and ongoing quality improvements. Drive mechanical design, prototyping, integration, testing, and final product release activities. Required Qualifications: Bachelor's degree in Mechanical Engineering. A minimum of 4-6 years of relevant industry experience in mechanical design, manufacturing engineering, or new product introduction. Proven hands-on experience in equipment assembly and/or hardware repair. Ability to work independently with minimal supervision. Excellent interpersonal, written, and verbal communication skills. Excellent documentation skills with attention to detail and quality. Results-driven mindset with a demonstrated desire to grow into roles with greater responsibility. This role is required to be onsite Monday-Friday. Candidates must have current authorization to work in the United States without the need for present or future sponsorship. You may be required from time to time to visit and work at PacBio locations and for such times as the Company considers necessary for the proper performance of your duties. All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, or on the basis of disability, gender identity, and sexual orientation. - #LI-Onsite Salary Range: $97,400.00 - $146,200.00 To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at PacBio. Staffing and recruiting agencies and individuals being represented by an agency are not authorized to use this site or to submit profiles, applications or resumes, and any such submissions will be considered unsolicited. PacBio does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to our jobs alias, PacBio employees or any other company location. PacBio is not responsible for any fees related to unsolicited resumes/applications. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, or on the basis of disability, gender identity, and sexual orientation. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact us at ************, or ****************************** for assistance. Visit our following pages for more information on: FAQs Benefits Culture Equal Opportunity Employment

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way - it's about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together: We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other The Position: The Clinical Laboratory Assistant's primary responsibility is to perform the lab support functions, helping other laboratory personnel during testing, and/or preparing samples for testing. This may include preparing labware and maintaining equipment, assisting with documentation, sample processing, and keeping the laboratories in a clean and orderly condition. ESSENTIAL DUTIES AND RESPONSIBILITIES: The Clinical Laboratory Assistant functions as a laboratory support team member. The main duties and responsibilities include the following, but not limited to: Under direct and constant supervision by a licensed, certified, or senior- level individual, as mandated by local regulations. Maintain flexibility, and work as a team player Assist in room and equipment maintenance in accordance with the laboratory's policies and procedures Prepare labware and help with stocking of laboratory supplies and reagents Assist in research and validation activities Archive samples by following the specimen storage and retention policies Create aliquots of reagents as needed using the appropriate lab equipment according to established protocols. Perform all duties according to guidelines outlined within the quality systems Compliant with company policies, procedures, safety requirements and regulations Take ownership and accountability of ensuring the highest quality of internal/external customer service Perform any other site/lab specific duties as assigned Who You Are: REQUIREMENTS: QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE High school diploma required A two-year college degree preferred Excellent problem solving skills Excellent written and oral communication skills Ability to work independently Exercise good judgment Excellent teamwork and collaborations skills Excellent interpersonal skills Aptitude and interest in laboratory work and orderliness At least one year experience in a laboratory setting preferred PHYSICAL REQUIREMENTS Repetitive movement of hands, arms, and legs Repetitive movement of fingers (typing and/or writing) Sitting, with occasional walking, standing, stooping, and moving about Exposure to general office and laboratory environment conditions Occasionally required to lift up to 25 pounds #LI-Onsite The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Pay range$28-$33 USDWhat We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. About Veracyte Veracyte (Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit **************** or follow us on LinkedIn or X (Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to ********************

. On-site cube available in South San Francisco or San Diego. We are seeking a talented and experienced AI/ML data scientist to join our Veracyte's Data Science team. This position offers a unique opportunity to work with experienced professionals to drive research and develop new diagnostic products employing one of the world's largest clinical cancer databases, encompassing multi-platform digital pathology, genomic and clinical outcome data. The successful candidate will develop digital pathology AI models for a wide range of clinical and pathology outcomes by applying and adapting state-of-the-art vision/vision-language foundation models to whole-slide images (WSIs). As a Data Scientist III at Veracyte, the candidate will be expected to assist in developing innovative solutions to complex problems under company's objective. This work will be conducted in close collaboration with other teams, including internal medical and business development teams, as well as key opinion leaders, with whom we collaborate on identifying relevant data, and developing computer vision models. The ability to explain AI/ML concepts to both experts and non-experts, including formal presentation, academic writing, and generation of publication-quality figures will be key necessary talents. The ideal candidate is passionate about data, eager to learn independently, and possesses strong analytical, problem-solving, and storytelling skills. KEY RESPONSIBILITIES: Develop digital pathology AI (DPAI) models with WSI data to predict clinical outcome and pathological/morphologic features, including adapting open-source state-of-the-art AI foundation models to Veracyte's data. Evaluate and analyze DPAI models with respect to clinical, pathological and genomic outcomes or features, with a view to linking explainability of model features to biology. Design and carry experiments to compare and evaluate DPAI methods. Document and explain the results. Collaborate with both internal and external partners to understand the clinical and business requirements for given products and tailor algorithms accordingly. Work with bioinformatician, statistician, and medical experts to document projects, including generating analyses and visualizations for publication in peer-reviewed journals. Who You Are: REQUIRED EXPERIENCE: PhD in Data Science, Machine Learning, Applied Math or equivalent field. 5+ years of experience of data/applied scientist role or equivalent Expert in Python or equivalent language for AI/ML development in the context of computer vision / DPAI (this includes data manipulation and preparation.) Experience in statistical analysis, especially in survival modelling and hypothesis testing (i.e., multivariate regression modelling with interaction effects). Experience working in cloud computing environments (AWS preferred). Demonstrated proficiency in summarizing and communicating findings from data, including an attention to detail when sharing findings. Ability to work effectively in a fast-paced and collaborative environment. Eagerness to learn new technologies and adapt to evolving requirements. RELEVANT EXPERIENCE (preferred but not required): Knowledge of cancer biology Proficiency with documentation and submission in regulated diagnostic environments (LDT or IVD). Experience working with real world clinical data. #LI-Hybrid, or #LI-Remote

Veracyte is seeking a highly motivated and experienced Senior Automation Engineer to join our growing Automation and Process Engineering team. This is a dynamic and impactful role where you will lead the development, optimization, and validation of automated liquid handling workflows-particularly using Hamilton platforms-for the implementation of molecular Laboratory Developed Tests (LDTs) in a regulated clinical laboratory environment. You will collaborate cross-functionally with R&D, Clinical Operations, Software, and IT teams to design and deploy innovative automation solutions that improve throughput, reproducibility, and efficiency. This is a unique opportunity to shape the future of molecular diagnostics through cutting-edge automation and process innovation. This is an onsite position based in our South San Francisco office. Responsibilities Design, program, and validate automated workflows for molecular assays using liquid handling platforms (eg. Hamilton) and other automated laboratory instruments Translate manual molecular protocols (e.g., RNA/DNA extraction, NGS library prep) into robust, high-throughput automated methods. Collaborate with Product Development, Clinical Operations, and Software teams to integrate automation with LIMS, bioinformatics pipelines, and data management systems. Lead portions or entire cross-functional projects from concept through implementation, ensuring timelines and deliverables are met. Collaborate with Equipment Engineering and Operations and QA on equipment qualification (IQ/OQ/PQ), calibration, and preventive maintenance procedures. Contribute to the development of custom 3D printed parts, software scripts, workcells, and novel automation technologies. Document workflows, SOPs, ERDs, and process maps in accordance with quality and regulatory standards. Provide technical mentorship and collaborate with internal stakeholders and external vendors. Who You Are: You've worked with both manual and automated molecular assays and feel right at home programming Hamilton systems. You might also have experience with microarray prep, NGS library prep, or RNA/DNA extraction from sample types like FFPE, blood, or cultured cells-that's a big plus. You know how to build automation workflows that work in a high-throughput, CLIA-regulated lab-not just in theory. You're good at spotting potential issues before they become problems, and you're the kind of person who enjoys figuring out how to fix things when they don't go as planned. You manage your time well, stay organized, and aren't afraid to try new approaches or take calculated risks. You enjoy working with others, sharing ideas, and solving tough problems as a team. Most of all, you're excited about using your skills to help push the boundaries of what's possible in molecular diagnostics. Required Qualifications Bachelor's degree in Life Sciences, Engineering, or related field. Minimum 5-7 years of industry experience in laboratory automation, with deep expertise in Hamilton Robotics platforms (preferred). Strong background in molecular biology techniques such as PCR, RNA/DNA extraction, microarray, and NGS. Proven experience designing, programming, and troubleshooting automated workflows in a clinical or regulated lab. Familiarity with CLIA, CAP, GxP, and 21 CFR Part 11 compliance. Excellent organizational, communication, and documentation skills. Ability to work independently and collaboratively across multidisciplinary teams. Proficiency in MS Office (Word, Excel, PowerPoint). Preferred Qualifications Experience with scripting languages (e.g., Python, C#) and database integration. Familiarity with Agile/Scrum methodologies and tools like Jira and Confluence. Experience with CAD design and 3D printing. Proficiency with Microsoft Power Platform and modern AI tools. Experience integrating automation with cloud-based data systems and bioinformatics pipelines. #LI-Onsite