51 jobs found in south san francisco

Overview Compass Transportation is one of the most respected and reliable transportation companies in the South San Francisco Area. We are an integral component of Transdev Corporation , the global leader in private transportation services with offices in 21 countries worldwide, and proudly serving the needs of commuters, tourists, and the public. Our employees are the best in the business, and are proud to work for a Global Leader in the Transportation sector. If you're looking for a career at an extraordinary company in an exciting city, Compass Transportation is the place for you! Why is Compass Transportation such a great place to work? We offer occupancy space for employees to watch television, relax, and sleep at their leisure. Dynamic people Exciting location Excellent benefits Great starting wage - $27.88 - $33.27 plus shift differential! M-F work week & weekend work schedules available Opportunity for advancement Responsibilities Available Opportunities : Monday thru Friday workweeks available. Weekend only jobs available too. Both full time and AM/PM part time/weekend jobs in our South San Francisco locations. Wage ranges include 10-20% split shift premium and overtime, if applicable. Benefits Overview ** Compass provides an excellent and competitive benefits package that includes health (medical, dental, and vision) and group life insurance, and flexible spending accounts.. We also offer 11 paid holidays , 7 sick days, and paid vacation depending upon years of service. Qualifications Must possessa valid CDL Class A or B with passenger and airbrake endorsements; Have a valid medical card Have a strong commitment to customer service and safety. Lifting, pulling and pushing are among the physical requirements of performing work in this position. Specific required limits of weight are determined by location site. Application Process Please ensure to bring a current copy of your Department of Motor Vehicle (DMV) H-6 report (no later than 30 days), valid commercial driver license, and current/valid medical card certificate with you, when you arrive to interview. For more information please visit our website at www.transdevna.com/careers The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions upon request. Transdev is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Applicants will receive fair and impartial consideration without regard to race, sex, color, national origin, age, disability, veteran status, genetic data, gender identity, sexual orientation, religion or other legally protected status, or any other classification protected by federal, state, or local law. EEO is the Law Poster: http://www1.eeoc.gov/employers/poster.cfm Drug free workplace If based in the United States, applicants must be eligible to work in US without restrictions for any employer at any time; be able to pass a drug screen and background check Job Locations US-CA-South San Francisco Posted Date 4 months ago (9/11/2019 5:26 PM) Requisition ID 2019-11207 Position Category Driver/Operator - Bus, Paratransit, Taxi, Limo, Shuttle Internal Code #TOD Internal Reference 307 Internal Code 3 Ind2 Company/Division Compass Transportation

Sr. Staff Program Manager, Software PortfolioRequisition ID: 111182BRWhen you re part of the team at Thermo Fisher Scientific, you ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you ll be supported in achieving your career goals.How will you make an impact?By leading a cross-business unit team to collaboratively define and deliver a division wide software strategy and portfolio built from market trends, user needs, technology assets and innovation opportunities. You ll make a critical contribution in delivering the right software to drive customer satisfaction and allegiance, revenue growth, and consumables attachment across the qPCR, CE, and Microarray platforms together with the associated Animal Health, Agrigenomics, Human Identification, Reproductive Health, and Clinical verticals.What will you do? You ll drive an initial and ongoing assessment of all current software product offerings and product development projects, providing specific portfolio recommendations and assisting the business units with software lifecycle management.You ll lead a cross-BU team through a state-of-the-art road mapping process and will provide a regular cadence of roadmap updates as the product development situation and competitive landscape evolve.You ll optimize resource utilization across the portfolio of active software technology incubations, new product introductions, and sustaining engineering projects; ensuring that the right projects are executed effectively.How will you get here?Education/Experience:Bachelor's degree in Biology, Chemistry, Physics, Computer Science, Engineering or Life Science required; SCRUM certification, PMP certification, advanced leadership training, MS, MBA or Ph.D. preferred.10+ years of experience across two or more of the following: life science or medical device software product development in Program Management, Product Management or R&D roles; experience with genetic analysis technologies and in-vitro diagnostics preferred.Fluent in English.Knowledge, Skills, Abilities:Intrinsically motivated, accountable, and committed to professional development.Excellent written and verbal communicator; exceptional relationship builder.Effective at influencing and leading without direct authority.Ability to lead and drive complex decisions and solve problems.Strong product development technical and business expertise.At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission enabling our customers to make the world healthier, cleaner and safer.Apply today! Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Associated topics: chief program officer, cpo, manage, manager, management, monitor, product manager, project manager, relationship manager, task

Principal Lead Cybersecurity Compliance - Digital Health Platforms South San Francisco California, United States of America Job ID: 201###-####36 Download PDF Apply For This Job Return to Search Results The Position Who We Are The Digital Health Platforms (DHP) group at Roche/Genentech is part of the Personalized Healthcare (PHC) Center of Excellence focusing on developing the next generation digital health platforms, tools and products for the future of medicine. Digital health promises to revolutionize how we diagnose disease, understand a patients disease course and response to treatment with unprecedented precision, and predict what treatment strategies are likely to be optimal. We are building a clinically validated, highly scalable and secure software platform that meet regulatory, quality, and privacy requirements. Our platform and services support Software as Medical Device (SaMDs), connected medical devices, and combination products. DHP partners across the company with other Digital Health groups to advance digital health solutions which include hardware, software, applications, tools, and platforms to enable development of our therapies as well as more personalized care of patients across a range of therapeutic areas. Our primary focus is on the validation, scaling, and productization of digital health platforms, tools, and products; inclusive of late-stage development of novel digital biomarkers and endpoints, as well as the design, conduct, and analysis of analytical validation, clinical validation, and clinical utility studies to meet stakeholder needs and regulatory requirements, as appropriate. The PHC Center of Excellence is focused on translating the promise of meaningful data at scale, advanced analytics, and digital technologies for drug development, and personalized patient care. The Position The Platform Compliance and Strategy (PCS) group within DHP leads the teams cybersecurity strategy covering the DHP platform and Software as a Medical Device (SaMD) applications, and the range of research, clinical and patient implementations that are anticipated to be productized. Products will have a customer focus, scaling from prototypes to commercial in-market deployment; making effective use of generated data is a high priority, facilitating deeper insights and ongoing product improvements. Enabling these outcomes securely is a key responsibility for the Cybersecurity Compliance Leader. We also closely collaborate within Roche with our other groups including: clinical development , other digital health groups, functions and subject matter experts within the Personalized Healthcare area and the Research and Early Development organizations (gRED, pRED & PD), Quality Assurance, Roche Diagnostics, Pharma Partnering, Informatics and privacy, cybersecurity & technology functions, in order to define and execute the strategic direction of Digital Health to transform drug development and patient care. We partner externally with patient groups and health care providers, technology companies, regulatory, policy makers and others. The Cybersecurity Compliance role has a leadership function as an advocate for DHPs information security needs. DHP creates digital products that are used in research, clinical environments, and by patients; the effectiveness and integrity of these products depends upon robust, end-to-end security and a coordinated effort by stakeholders across Roche. At the back-end, security-by-design ensures that the DHP platform has been crafted to be secure; at the front-end, design thinking validates that clinicians and patients can trust that their interactions and data remain private. This hands-on individual will own cybersecurity for the full product lifecycle. Their remit will include: defining security plans and requirements for the DHP platform, supporting requisite compliance and regulatory needs, and advocating across business and industry for a strategic view on delivering personalized healthcare to millions with improved outcomes. Our intention is to align the tactical design decisions made in building the DHP platform with the digital health regulations and policies that Roche advocates. Responsibilities Cybersecurity Leadership + Work collectively across stakeholders in Genentech and Roche to craft a risk-based framework which informs cybersecurity requirements and standards for the companys digital products + Lead and participate in security risk assessments as part of the digital product lifecycle + Act as the product owner for security across the technology teams by working with other groups and stakeholders to prioritize security-related work on the DHP platform, and on digital health products that are part of the DHP portfolio + Establish, lead, and be an active partner on a cross-functional Security Incident Response Team, and associated standard operating procedures, to rapidly investigate and address security incidents that arise + Keep abreast of healthcare industry security trends and developments + Coordinate cybersecurity policy positions across Roche policy and regulatory affairs groups Architecture + Partner with product and technology teams to ensure that technical designs will lead to secure implementations + Liaise among enterprise IT, Platform Architecture, Product Development, Cloud Service Providers, and Legal Manufacturers to build end-to-end alignment for cybersecurity + Provide deep technical understanding of security systems at different layers, including: network, cloud, endpoint, advanced malware defense, and data security Compliance + Establish governance, risk management and compliance frameworks for digital products developed by DHP + Establish, and lead, and be an active partner on a working group to determine how the companys digital health products will address the five trust principles in SOC 2; lead DHPs activities to ensure compliance with SOC 2 + Prepare DHP to satisfy the requirements for the HITRUST Common Security Framework; align stakeholders and executive sponsors for HITRUST certification. Develop a plan to efficiently manage ongoing compliance costs, and lead DHPs HITRUST certification + Develop a cybersecurity audit plan, collaborate on company implementation/standard development and oversee independent penetration testing of the network, application and device + Minimum Qualifications + Passionate about using technology and data-driven approaches to help improve the lives and health of our patients + Working experience with software, digital health, and/or cybersecurity aspects of digital health + Bachelors degree in a technology field, an auditing discipline, or equivalent practical work experience + 6+ years experience in software engineering management, product design management, and/or IT infrastructure management + 4+ years leading cybersecurity compliance efforts thorough in-depth understanding of standards and certification frameworks, including: NIST CSF, NIST 800-53, FISMA + Knowledge of platform network security + Experience in Cloud Security + Experience in software component security + Experience in data encryption and data access security + Familiarity with GDPR, HIPAA and implementing rules for data sharing across regions + Demonstrated ability to develop and implement cybersecurity strategic plans + Security certifications such as ISC 2 CISSP, SANS GIAC, or CompTIA Security + + Demonstrated experience in building stakeholder consensus and support for technical compliance + An entrepreneurial mindset, tolerance for ambiguity, and a predilection for self-direction + Track record of effectively working in a matrix environment with global team members coming from scientific, business and technology backgrounds, using influence without authority + Customer-centric behavior, experience in employing design-thinking, and deep interest in serving patients + Excellent written and spoken communication in English + Ability to travel domestically and internationally up to 20% time Preferred Qualifications + Masters degree or greater, with at least 5 years experience as described in minimum qualifications , above + Accomplished at leading a complex organization through HITRUST Certification + 2+ years leading compliance activities associated with HIPAA, ISO/IEC 27032, and/or HITRUST + Experience in addressing compliance for medical devices and/or Software as a Medical Device + Experience in security for product development, and a certification such as ISASecure CSA + Familiar with wearables and IoT devices Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page. Who We Are A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work. The next step is yours. To apply today, click on the "Apply online" button. Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page. Return to Search Results Associated topics: forensic, identity access management, iam, idm, information technology security, phish, security, security engineer, threat, violation

Hello We have a new requirement with one of our client for Product Manager Sharing the Job Description with you Title : Product Manager Duration : 6months Location: South San Francisco, CA Required Qualifications: 9 years experience in Product Management required with 4 years experience in regulated instruments Product Management required Bachelor s degree in Biology, Biochemistry, Science OR Bachelor s degree in business, marketing, or related degree Outstanding written and verbal communication skills are required Track record of success in launching solution oriented products as a system required Demonstrated ability to develop business cases, financial model, customer and product requirements for strategic and/or complex products, soliciting and integrating Voice of Customer and User Centered Innovation inputs Demonstrated experience successfully managing products, pricing, and forecasting Strong leadership skills within cross functional teams; a demonstrated leader through influence with strong negotiation skills Is customer-centric and keenly aware of markets, trends and competitors Is authentic, transparent and leads by example, holding self and others accountable Organized with strong project management skills Demonstrates a sense of urgency, contagious optimism and a can do attitude Inspires, motivates and collaborates with others; team-first attitude Stretches across borders, breaks silos and builds effective partnerships with customers and colleagues Regards Vinay KM Indecomm Digital Services ( : 917-###-#### Email: 8800 E Raintree Dr, Suite 200, Scottsdale, AZ 85260 / - provided by Dice

Full Description: IT Manager / Sr. Systems Administrator Our client is for an IT Manager for their office in South San Francisco. They are looking for someone who can help them implement new Saas apps as they move towards commercialization. An ideal candidate will have many years of experience in an IT role 8 years experience supporting computer systems on a variety platforms Expert knowledge of Active Directory and Group Policy Objects Experience with AirWatch MDM, AWS or Azure, BitLocker, and MBAM Proficiency with layer 3 switches and subnet routing BA/BS in computer science, management information systems, or an equivalent Are you available? Please send your most current resume to resumesmbg.com Please reference JO17069 Mainz Brady Group provides technology staffing solutions to the best known companies in Software Development, Finance, Electronics/Manufacturing, Retail, R&D, Services, Biotechnology, Healthcare and Telecommunications. We specialize in Information Technology, Technical Sales and Marketing Staffing on a Contract, Contract to Hire, and Direct Hire basis. To see a complete listing of all current openings please visit us at www.mbg.com/ To download our FREE Mobile Apps "MBG Jobs", visit www.mbg.com/mobileapps dice - provided by Dice Associated topics: chief program officer, cpo, manage, manager, management, monitor, product manager, project manager, relationship manager, task

The Product Manager will develop multi-generational product strategies and guide planning for future positioning, growth, and development of disruptive advancements in synthetic biology. This includes assessing and prioritizing customer and market requirements, working with strategic collaborators, research & development, operations and the wider commercial team to deliver truly innovative products. The product manager is ultimately responsible for revenue, margin, customer satisfaction, and market share objectives. What Youll Be Doing In collaboration with the commercial team, the product manager will own and be responsible for growing the synthetic biology product portfolio Work closely with customers and strategic partners to gather input to develop disruptive new products Develop detailed product strategy and roadmaps to meet company financial and strategic objectives Build business plans and strategy for the application area that includes opportunity assessment, positioning strategy, financial analysis, and required tactical plans to support successful product adoption Deliver on an ongoing basis the product requirements with associated prioritization, metrics, and supporting analysis Work very closely with development teams to ensure successful implementation of product requirements and drive product development to commercial launch Perform ongoing competitive and market analyses Train the sales teams and support selling activities as appropriate, including the development of sales tools and collateral Create content collateral and product messaging to convey the value proposition to target markets Provide input to partnership opportunity assessments Manage collaborations with key partners and customers to rapidly develop innovative gene synthesis solutions and support broader product adoption What Youll Bring to the Team Track record of success defining and launching products in the research tools marketplace with a deep knowledge of synthetic DNA preferred Must speak DNA Understanding of gene synthesis technologies, workflows including current and future applications Proven ability to influence cross-functional teams, and to work effectively with customers, development, and sales teams A successful candidate will have both molecular biology and product management experience Demonstrated track record of managing high profile collaborations that deliver successful products Experience with building product roadmaps and product life cycle management Experience with financial modeling and data analysis skills. Ability to build and analyze models to forecast and track results 3-6 years of relevant work experience in the life sciences or a related field, with at least 5 years in product management and/or product marketing positions Degree in molecular biology, genetics or associated scientific field required. Outstanding leadership, teamwork, and communication skills Hands on, high energy, proactive attitude Ability to travel up to 20% both domestically and internationally Preferred Qualifications PhD and/or MBA is a plus Experience of working with DNA synthesis Associated topics: chief program officer, cpo, manage, manager, management, monitor, product manager, project manager, relationship manager, task

The Position POSITION SUMMARY As a DATA MANAGER within our Clinical Data Management (CDM) function you will work within a team of experts in data life-cycle management who acquire and curate data for use in exploratory research, clinical development and evidence generation. You will collaborate with peers within the function and across the organization to identify, design and execute fit for purpose data management solutions, adhering to F.A.I.R. (Findable, Accessible, Interoperable, Reusable) principles. You will ensure the timely completion of data management deliverables and partner with Functional Service Providers (FSPs) and vendors, overseeing and providing technical expertise in the delivery of high quality data. You may also contribute to functional, cross functional, enterprise-wide or external initiatives that shape our technical landscape, business and healthcare environments. You will need strong strategic, collaboration and communication skills, as well as an entrepreneurial mindset, to evolve the way we collect and deliver data and to develop and deliver medicines for our patients. Job Levels Data Manager: As Data Manager you will be accountable for study/studies and non-study project deliverables. You partner with cross-functional teams and external partners and work with considerable independence. Senior Data Manager: As Senior Data Manager you will lead/contribute to the development of new concepts, technologies, and standards. We will look to you as a positive role model for peers and you will support colleagues to improve in their role with both technical and interpersonal skills. Principal Data Manager: As Principal Data Manager you will be expected to lead/contribute to broad CDM strategies, lead and deliver on complex projects, and interact with external partners. You will proactively share learnings/experience with colleagues both internal and external to the function. Responsibilities PROJECT MANAGEMENT : Develop risk management strategies and proactively manage timelines to ensure successful oversight and delivery of studies, projects and coding responsibilities, including the implementation and adoption of new technologies. STAKEHOLDER MANAGEMENT: Proactively engage with stakeholders across the business to understand their needs and influence their understanding of decisions made in our function. Inform stakeholders of status of key deliverables and act on changing milestones. VENDOR MANAGEMENT: Partner with relevant functions for external data vendor selection and management. Oversee development of data transfer agreements with vendors ensuring use of standards, fit-for-purpose data models and transfer intervals. DATA COLLECTION AND ACQUISITION: Act as experts for data collection, advising teams and stakeholders on best practices and proposing innovative solutions. Ensure a high quality of data and compliance with applicable pharma industry regulations and standards. PROVIDE DATA SOLUTIONS: Stay current with and adopt emergent data collection, data management, visualisation and provision tools and applications to ensure fit-for-purpose and impactful approaches. Deliver on solutions as needed. DATA QUALITY REVIEW: Use data surveillance tools and strategies to provide aggregate level reviews designed to identify patterns or anomalies in our data to ensure high quality results. DATA CURATION: Organization and integration of data collected from various sources. Maintain value of data through application of FAIR (Findable, Accessible, Interoperable, Reusable) principles. SUPPORT ANALYSES: Partner with stakeholders to understand their data insight needs and offer Data Management solutions. Demonstrate a strong understanding of the data flow from collection through to analysis and filing. FUNCTIONAL EXCELLENCE : Collaborate and contribute to functional/cross-functional initiatives or goals to promote new ways of working, including emerging technologies. Enable broader and more effective use of data to support the business. TECHNICAL CONSULTANT : Offer guidance and advice to peers within the function, to key stakeholders and to FSPs, CRO and collaborative groups on technical solutions to ensure high quality data collection and delivery. Deliver on solutions as needed. Minimum Qualifications BSc or MSc in Life Sciences, Data/Computer Science, Bioinformatics OR equivalent industry experience. Demonstrated strong collaboration and excellent communication skills both written and oral (proficiency in English required). Knowledge of CDISC data standards. Knowledge of ICH-GCP and working in regulated environments. Project Management skills. Able to manage multiple requests and priorities. Demonstrated leadership capabilities around decision-making, negotiation, motivation (self and others) and influencing. Experience with data analytics and/or visualization tools and techniques. Demonstrated entrepreneurial mindset and self-direction, ability to mentor others and willingness to learn new techniques. Knowledge of biological principles, display interest and demonstrate scientific curiosity including an understanding of data types and their scientific use ( clinical, biomarker, WGS, RNA-seq, etc.). The skills below include the specialities for all activities, tasks and responsibilities. Some (not all) will be required by individuals depending on the tasks performed and needs of business. Preferred/Additional Qualifications Experience in leading CDM study teams and maintaining oversight of all start-up, conduct and close-out activities for multiple or complex studies, ensuring fit for purpose quality (including oversight of FSPs, Vendors, CROs and Collaborative Groups). Experience in leading the collection of clinical trial and/or Real World Data. Good understanding of molecule and disease area strategies, healthcare environments, as well as strong scientific and technical expertise. Extensive [technical] and/or [industry] experience required for senior/principal roles. Experience in enterprise level operating systems and familiarity with databases (Relational Database Management System, RDBMS). Fluency in programming languages (SAS, R, Python, SQL etc.). Some experience with advanced analytics approaches (e.g. machine learning, AI). Experience with tools related to technologies required to undertake analyses on large data sources or with computationally intensive steps (SQL, parallelization, Hadoop, Spark, etc.). Experience producing interactive outputs (e.g. Shiny, Tableau). Contributor to open source packages, libraries or functions. Experience implementing reproducible research practices like version control (e.g., using Git, Rmarkdown) and literate programmer. Experience with SDTM implementation and CDISC standards. Experience with standardized terminologies such as MedDRA and WHODrug BSN, RN, RPh, Pharm D, PA or other applicable health professional qualification preferred or previous practical and theoretical experience of clinical coding This is a local hire only designated position, as relocation assistance is not available for the position #LI-PDBA1 Who We Are A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work. The next step is yours. To apply today, click on the "Apply online" button. Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page. Associated topics: data administrator, data center, data engineer, data integrity, data management, data quality, data scientist, data warehouse, database administrator, hbase

Overview Myriad is an industry-leading clinical genomics company that has helped millions of patients andtheir families benefit from advanced and accessible DNA and RNA testing. We are the pioneersof hereditary cancer screening, which informs patients of their risk for cancer via next-generationsequencing of key genes. We have since augmented our portfolio with products that helppatients with everything from selecting appropriate medication for depression to understandingtheir risk of having a child affected with severe disease. We eagerly pursue cutting-edgegenomic technologies that can ultimately empower people to make informed health decisions.Our clinical development and science teams are collegial and interdisciplinary, attracting scientists from the top universities and research centers. We are seeking a Computational Scientist with strong analytical tools from any area of biology to join us in the South San Francisco office. Responsibilities What you ll do: Design and perform analyses for publications to drive the clinical development across 14 products, leveraging large datasets including both clinical and laboratory data Serve as the expert scientist who can turn a hunch or intuition your own or a colleague s into a rigorous quantitative analysis Work closely with different groups across the organization, e.g., medical affairs, biostatistics, clinical operations, marketing, and sales across different products Communicate scientifically complex topics to diverse stakeholders across the company and externally through academic and clinical conferences Influence the medical guidelines that impact the lives of millions of people. Thrive on handling diverse projects with a range of time-scales. Qualifications Suggested Qualifications (feel encouraged to apply even if not all are met): PhD (or equivalent experience) in Computational Biology, Biophysics, Mathematics, Physics, Computer Science, Statistics, Molecular Biology, Genetics, or related discipline. Well versed in computational analyses with large datasets and making quantitative arguments from first principles. Computational skills, preferably with fluency in Python or another scripting language. Track record of peer-reviewed publications in well-respected journals; we re especially interested in those where you played a driving role. Excellent communication via speech, text, and graphics. Strategic thinker and implementer A sense of humility and an eagerness to contribute to a supportive, interdisciplinary team The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is frequently required to sit; talk; or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and stoop; kneel; or crouch The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision and depth perception. About Our Company Myriad Genetics Inc., is a leading personalized medicine company dedicated to being a trusted advisor transforming patient lives worldwide with pioneering molecular diagnostics. Myriad discovers and commercializes molecular diagnostic tests that: determine the risk of developing disease, accurately diagnose disease, assess the risk of disease progression, and guide treatment decisions across six major medical specialties where molecular diagnostics can significantly improve patient care and lower healthcare costs. Myriad is focused on three strategic imperatives: maintaining leadership in an expanding hereditary cancer market, diversifying its product portfolio through the introduction of new products and increasing the revenue contribution from international markets. For more information on how Myriad is making a difference, please visit the Company's website: www.myriad.com. Myriad is an equal opportunity employer and as such, affirms in policy and practice to recruit, hire, train and promote, in all job classifications without regard to race, color, religion, gender, age, sexual orientation, gender identity, national origin, disability status or status as a protected veteran. Reasonable accommodation will be provided for qualified individuals with disabilities and disabled veterans in job application procedures. We believe that diversity lends a regional, national, and global advantage to the clients we serve. Our workforce consists of dynamic individuals, with a range of backgrounds, talents, and skills. Associated topics: .net, application, backend, back end, devops, java, matlab, sde, software programmer, sw

Job Description Informatica MDM Tech Lead / DA , South SFO, CA Job Title: MDM Tech Lead / DA Job Location: South SFO, CA Duration: 1+ Years Duties: Demonstrates extensive knowledge and interaction with end users to understand and document business and functional requirements for complex projects in Customer Master data management and Field Alignments Demonstrates experience working with technical teams across the full software development life cycle. Demonstrates extensive knowledge and exposure to the following Master data and Alignment concepts : Data Cleansing & Standardization Process Data Integration & Data Enrichment Hierarchy Management Custom UI Sales alignment & Employee assignment Incentive Compensation process Skills: Strong SQL skills. Experience with MDM Tools like Informatica or Reltio. Experience with Sales/Field Alignment process and Incentive calculation for sales team Familiarity with Alignment systems like JAMS, Organization Management etc Full understanding of various MDM domains like Customer, Product and Organization and their data models Experience with data profiling to understand rules for match/merge, DQ and hierarchy management Demonstrated experience in methodologies and processes for managing large-scale databases. Understanding of addressing and metadata standards. Experience with Continuous Integration/Continuous Deployment pipelines Background working in an agile delivery framework Ability to work with stakeholders to assess potential risks Excellent interpersonal, written communication, persuasive and presentation skills. Associated topics: chief program officer, cpo, manage, manager, management, monitor, product manager, project manager, relationship manager, task

Lead on clinical studies and manage/provide training to lower level personnel when needed. Contribute and implement to statistical analysis plans; provide additional expertise in the analysis of clinical trial when it relates to protocol development, case report form design and data collection. Review Data Management Plan, Data Transfer Plan, Data Validation Plan and Edit Check Specifications and provide comments. Work closely with Biostatistics to create analysis specifications following the instructions provided in Statistical Analysis Plan (SAP) Create CDISC SDTM and ADaM files, SAS export files, Define.xml and Reviewer's Guide for Electronic Submission. Perform Data analysis, statistical analysis, generate safety and efficacy tables, listings and graphs using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS. Interact with Statisticians and other clinical team, perform ad hoc analysis and generate outputs according to the requirements. Help identify issues and initiates resolution of the problems. Act as a liaison between statistical programming, subcommittees and project teams as needed. May serve as external spokesperson for the organization. Create/acquire tools to improve programming efficiency or quality. Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues. Experience with integrated summaries (ISE/ISS) and Clinical Study Reports. Qualifications: Ability to use professional concepts to achieve objectives in innovative and efficient ways. FDA submission experience is a must. Experienced in managing programming staff. Solid knowledge of CDISC standard (SDTM & ADaM). Experience: Minimum 7 years Pharmaceutical/Biotech programming experience NDA submission experience is a plus. Strong SAS programming and Statistical background along with experience with SAS Base, SAS/Macros, SAS/Graph and SAS/Stat. Education Requirements (degree, certifications, etc.): Include must have and preferred BS/MS in Statistics, Math or Scientific Discipline. Associated topics: biostatistics, data analyst, probability, statistics, c

Job Description About Us Pliancy provides white-glove, high-touch IT consulting services to Life Sciences and Finance organizations (Venture Capital, Private Equity, and Hedge). As a people-first company who invests in the long-term success of our employees, were looking for creative thinkers who like to solve interesting problems. Anyone can sell solutions, right? Wed rather find the right solution for our clients by discovering their unique needs and applying them to the bigger picture. We challenge the status quo to innovate towards simplicity and sustainability thats what sets us apart. That, and our Cloud Native-first approach, which is still rare among our legacy-solution-bound competitors. Whether streamlining a clients race to a cancer cure or securing the fine details of data integrity, were driven to help people. Plenty of opportunity for out-of-the-box thinkers looking to grow their career. What's an average day like? The clients you'll work with are exclusively Life Science and Capital Management firms (likely Venture Capital, Private Equity, or Hedge Fund). These clients are very friendly and enjoyable to work with. You're treated as one of their own, not as an outside individual. We're a fun, relaxed team who has a passion for technology and helping our clients through creative solutions. If you love a challenge, building relationships, and socializing with fellow team members you'll love our culture. A typical week is a mix of four-hour to eight-hour scheduled visits consulting with your primary clients, researching solutions, implementing projects, using technology to improve process and workflows, improving documentation, training users, and responding to ad-hoc requests. You'll also enjoy catered lunches onsite or meet up with teammates nearby for meals and coffee. When not scheduled at your clients' sites, you may drop in at the local office to collaborate with a coworker on pending issues. The remainder of the time is spent with the team on internal solutions, special projects, ticket escalations, and learning new technologies. Who are we looking for? You're an attentive, sociable person who loves connecting with the people you support and working in a team environment. To you, clients are people, not cases to solve you build relationships, and as a by-product, you build trust. Few things make you feel better at the end of a workday than helping your team work swiftly and efficiently toward a common goal. You look out for your people and theyre grateful for your responsiveness. You enjoy solving business problems through the clever use of emerging technologies, often pioneering the adoption of these tools. Responsibilities: Driving the adoption of forward thinking technology in a rapid growth environment Identifying unique cutting edge solutions to business problems leveraging technology Providing high touch white glove responsive support to executives, executive assistants, and staff Troubleshooting day to day technical issues and assisting with daily requests Creating new users, configuring laptops, and setting up their desks/workstations Training and assisting on use of tools and technology to meet business needs Documenting assets, configurations, passwords, processes, etc. and maintaining current and accurate documentation Assisting with office moves, upgrades, and AV deployments Requirements Must Have Soft skills (Personality, Relationship Building, Communication Skills, Stress Management) Experienced and comfortable supporting executive teams Intimate Windows and MacOS knowledge 5+ years of general IT support experience Incredible sense of pride and passion for what you do and a desire to help your teammates Aptitude (Ability to learn new technologies quickly) Troubleshooting (Ability to work through issues methodically) Ability & willingness to properly document processes and assets Active Directory / Azure AD Cloud based services (O365 / GSuite / Box / Egnyte and others) General understanding of networks including wireless mesh networks Authorization to work in USA for any employer Nice to Have Cloud based services (AWS, GCP, Azure) Prior experience supporting Capital Management firms (VC/PE/Hedge) Experience with cloud ID services, Okta / DUO and other MFA/SSO providers Video-conferencing/AV experience Addigy/Jamf/Intune PowerShell & Scripting VoIP Support & Management Benefits Compensation & Benefits Generous salary, above average pay (100K-130K dependent on experience) Cadillac healthcare: Anthem Blue Cross Gold Plan (Premiums 100% covered for employees, 50% for dependents) Medical HRA: Company funded reimbursement account to help cover copays, deductibles, and coinsurance Dental / Vision HRA 401K + 6% Matching (available on Day 1) Health/Wellness Reimbursement up to $100/mo Cell phone & home internet covered (reimbursement) Commuter benefits Unlimited vacation policy Why us? High profile clients / unique challenges / best in class hardware & technologies Competent and fun co-workers who take team work seriously Rapid company growth 33%+ year over year Limitless potential for those who go above and beyond Flexible schedule for those who are organized self-starters and are good at self-management Great culture of working with talented people, we really do treat our people as family Clothing allowances, lunch allowances, and other perks Associated topics: business, business advisory, business analysis, business analyst, business systems, business systems analyst, client, consult, consultant, market

As an IT Business Partner for the Scientific Decision Support Network in PD Informatics you will work closely with the Roche Immunology, Infectious Diseases and Ophthalmology Therapeutic Area (I2O) teams, developing the business understanding to effectively support opportunities enabled by Information and Technology. I2O is part of the larger Clinical Science (PDC) organization whose mission is to develop and execute innovative and robust product development programs to deliver well-characterized and differentiated medicines to patients with medical need.What you ll be working onYou will partner with business stakeholders in the I2O TA and co-create technology-enabled business strategies/cases with colleaguesProvide strategic direction, prioritization, mobilization of resources aligned to shared business objectives with respective areasActively participate in strategy setting meetings in PD Informatics, Scientific Decision Support and across InformaticsTake leadership role that educates, advises and challenges to enrich business area strategy for the benefit of the wholeNegotiate and influence to ensure the right product managers and product owners are assigned to key initiativesUnderstand the data needs of I2O TA and offer data solutions to enable stakeholders answer scientific questionsProactively identify business opportunities and work with business and Informatics partners to architect, design, prototype and deliver continually improved productsThe ideal candidateHas business domain knowledge of Pharma Late Stage Clinical Science, specifically around using different types of data to enable data driven decision makingNurtures and develops a collaborative, consultative and value driven partnershipHas an understanding of, and practical experience applying, advanced analytics, machine learning and artificial intelligence techniques to solve Drug Development challengesExhibits a high degree of self-awareness, empathy, listening, active curiosity, awareness of different norms and expectationsWell-networked, has a cross-organization perspective, connects the dots and adds the external perspectiveExhibits an Agile mindset in the approach to work, i.e.:Enables a diverse group of partners to speak with a single voiceGood enough instead of perfectionFocus on Reuse before Buy before Make when providing direction on future solutionsExhibits intellectual curiosity and integrity and has strong passion to bring value-adding technology to the business. Exhibits strong soft skills typically required as an Informatics Business Partner (i.e.: active listening, influencing, challenging the status quo)Understands, for example, the protocol development and medical data review requirements and is keen to find automation opportunities in such business processesQualificationsMaster s degree in Computational Biology, Bioinformatics, Statistics or related experience; PhD a plus.Familiarity with R, Shiny, Python, Spotfire and other analytical tools advantageousSolid understanding of global Late Stage Drug Development and ideally of the disease areas in the scope of I2OAbility to travel up to 20%Full time Associated topics: artificial intelligence, c++, c#, c c++, information technology, matlab, photonics, processor, python, schematic

Requirements: BS in Computer Science or Math or equivalent experience At least 2+ years of experience in cryptocurrency 4-7 years building data pipelines using Spark in: Scala Ignite Kafka Yugabyte Cassandra Required Skills for all Data Science Team Candidates: 1. Solid development foundation >= 7 years developing highly usable analytics tools 2. Highly self-directed & able to work a project from conception through delivery (e.g. from formulation, execution and evaluation of the research through to development and integration into prod) 3. Good understanding of the blockchain technical space and data structures >= 4 years analyzing relevant data structures (i.e. in tabular, or network forms) 4. Clear dedication to continuous learning 5. Python, Jupyter, Scala, Avro, Spark, Ignite, Kafka, Cassandra, Yugabyte 6. > 2 years Experience in large-scale network analysis, graph databases implementation at scale Associated topics: application, backend, back end, c c++, c#, matlab, perl, python, sde, software engineer

Job Description Encoded Therapeutics Inc. is a biotechnology company advancing precision medicines for a broad range of genetic disorders. Our mission is to unlock new opportunities for viral gene therapy through genomics-driven discovery. We focus on delivering life-changing advances for individuals with genetic disorders not addressable with current approaches. For more information, please visit www.Encoded.com. Reporting to the Senior Director, Biometrics the Senior Manager/Associate Director, Clinical Data Manager is responsible for the data management aspects of clinical trials. The Director, Clinical Data Management will oversee all activities of data management in all or some development programs including, collaborating and supervising vendors, working closely with CROs, clinical operations and collaborating with spearheading relationships with vendors with regard to clinical trial database and ensuring the integrity of data and analysis. Primary Responsibilities Reviews protocols from a CDM perspective and provide functional-expert feedback Review and approve key clinical data management deliverables generated by a DM vendor, including: Case Report Form (CRF) design, CRF completion guidelines, database design specifications, data entry guidelines, data management plans, edit check specifications, serious adverse event reconciliation plans, medical coding, data listing specifications, and electronic data transfer agreements Manage/oversee study setup, testing and system validation for new studies in partnership with the DM vendor Oversee data cleaning activities executed by the DM vendor and ensures protocol-specified guidelines are applied to the review and cleaning of clinical data Collaborate with internal Data Science (statistical programming), internal Biostatistics, and internal Medical Monitor on identifying critical variables in the clinical dataset, for protocol-specified endpoints. Coordinate implementing these variables into DM vendor activities Develop and manage timelines for key clinical data management deliverables in coordination with the clinical data management vendor and Encodeds project team Coordinates with partner functions and counterparts at CROs, central laboratories, and other service providers to ensure study objectives and DM timelines are met Monitor vendor performance to ensure timelines and data quality standards are met Ensure compliance of clinical data management processes with applicable regulations and guidelines The Clinical Data Manager will need to be familiar with CDISC SDTM standards and SAS/Excel Data extracts and data cleaning listings Stays abreast of all requirements of EDC and electronic submission Utilizes EDC platforms such as RAVE, InForm, Data Track, etc. Requirements A minimum of a B.S. degree in biology, nursing, computer science, or related field and 8+ years experience as a Clinical Data Manager in a pharmaceutical or biotechnology industry and 3+ years experience as a Senior Manager or Associate Director within a Clinical Data Management group. Experience with various database systems and electronic data capture Understanding of relational database and ability to function individually as well as a member of a team Strong understanding of clinical trials and regulated and GCP compliant working environment and documentation Demonstrated experience with IWRS A thorough understanding of coding dictionaries and various required reconciliations A thorough understanding of central and local labs and their different requirements Strong understanding of requirements of a fast-pace environment and need for change as deemed necessary Excellent at prioritizing, understands timelines and working within budget Demonstrates positive attitude, able to follow instructions and always reliable Builds strong professional relationships and work with internal and external partners Exceptional flexibility and a proven track record of adapting to change Successful experience in starting and locking database Very familiar in working with vendors and Data Transfer Plans Proven experience developing, modifying and following SOPs Successful Experience handling and managing Regulatory Agencies as related to data management documentation, audits, and requirements A good communicator and writer, creative and intuitive Organized and prioritizes tasks, delegate or escalate as needed Proficiency in Word, Excel, and PowerPoint presentation Preferred Skills and Experience Familiarity with rare disease drug development Benefits Comprehensive benefits package, including competitive employer premium contributions Meaningful stock option grants PTO, sick time and holiday pay Generous Parental Leave program Pre-tax medical and dependent care programs STD, LTD, Life and AD&D Professional development opportunities Team-building events Fully stocked kitchen Purple Tie dry cleaning service Fitness center Encoded is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Encoded is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Encoded are based on business needs, job requirements and individual qualifications, without regard to race, religion or belief, color, national origin, gender, status as a protected veteran, status as an individual with a disability, or any other status protected by the laws or regulations in the location in which we operate. Encoded will not tolerate discrimination or harassment based on any of these characteristics. Encoded encourages applicants of all ages. If you need assistance or an accommodation due to a disability, you may call us at +1 650-###-####. Associated topics: demand, government, lead generation, market, marketing, marketplace, newspaper, solicitation, twitter, university relationship

Position: Senior Web Developer/Creative Engineer Location: Bay Area, CA Duration: Long Term Responsibilities: Architect, design, develop, and maintain innovative, engaging, and informative websites for a worldwide audience. Advise, collaborate with, and synthesize feedback from Marketing, Product, and Engineering partners. Have a voice in the design process and contribute UX design feedback. Skill/Experience/Education Mandatory 6 years of experience developing websites and applications. BA/BS degree or equivalent practical experience Advanced Javascript skills including data structures, algorithms, and object oriented implementations. Intimate knowledge of the front end stack and the latest web standards including ES6, HTML5, and CSS3. Experience with the Angular framework (, not to be confused with the older AngularJS framework) Experience with mobile development including responsive design and page load optimization Experience writing Javascript unit and/or end to end tests Cross discipline communication and organizational skills Coding consistency and attention to detail Desired Typescript - Python Experience implementing accessibility standards Contributions to open source Sass, Gulp, Node.js Protractor, Jasmine, Karma Coding to a style guide & linting DevOps (build systems, project scaffolds) Git workflows (branching models, merge tools, release versioning) Requires Angular code samples/GitHub to be considered Associated topics: angular, ajax, d3js, ecmascript, frontend, json, php, web application, web application programmer, website

Job Description Sr. Manager, Clinical Data Management Description Position Summary: The Senior Manager, Clinical Data Management at Portola has broad study data management responsibilities including but not limited to study start-up through database lock and clinical study report. The successful candidate will deliver high quality data, on time and on budget. This role will report to the Senior Director, Biometrics. Responsibilities: Manage group of internal data managers; mentor and develop direct reports Responsible for ensuring the data collected meets the requirements of the study objective and company quality standards Ensure that the clinical study efforts are aligned with business objectives and comply with FDA requirements Lead or provide oversight to technical infrastructure of the clinical programming and EDC environments with Development IT, contribute to strategy for integration of systems, including DM systems (EDC, CTMS, Data Warehouse, etc.) and partner systems (CTMS, IVRS, Safety database, etc.) Lead CDM Systems activities (EDC, Study Build, Clinical Programming) Partner with clinical study team to create and validate database design, edit check specifications, data transfer specifications, and clinical listings and reports Develop and implement strategy for the improvement of productivity and standardizing of study build and programming activities Determine documentation and archival standards of CDM Systems deliverables including DM systems, databases, programs, and specifications Working with IT, ensures that local IT infrastructure meets Biometrics/Data Management needs and global standards Develop, apply and promote consistent standards through standard processes and SOPs Ensure guidelines and specifications on validation procedures and data transfer procedures are followed Maintain appropriate documentation surrounding maintaining or archiving clinical data Assist with identifying suitable vendor(s) for outsourcing data management activities and coordinate the review and approval of Master Services Agreements Work closely with CROs to prepare and ensure proper execution of data management plans; manage data management projects from beginning to end Work closely with Clinical Operations group, statisticians, SAS programmers and other staff as appropriate to collect complete and accurate data required for database lock and statistical analyses Communicate with all departments regarding project statuses/issues; provide ongoing feedback on data management workflows to increase efficiency and provide feedback to CRAs Oversee interactions with outside vendors (e.g. clinical laboratories) on collection, transmittal and transfer of study specific data Manage multiple and varied tasks; prioritize workload with attention to detail Author documents such as Standard Operating Procedures (SOPs) and other departmental work processes Qualifications: M.S. degree in relevant field (or equivalent experience) with 8- 10 years experience in a clinical research data handling environment with relevant practical experience in protocol review/CRF design, clinical study databases and data management, preferably in the biotech and/or pharmaceutical industry Strong well-rounded technical skills: EDC, SAS, and CDISC Knowledge of lab/image data and other external data sources Strong scientific background and understanding of clinical trials, pharmaceutical operations, and regulatory compliance Practical knowledge of ICH, FDA, and GCP regulations and guidelines; Demonstrated success in leadership roles contributing to critical regulatory submissions such as safety updates, FDA requests, and/or briefing documents Strong scientific background and understanding of clinical trials, pharmaceutical operations, and regulatory compliance Experience in leading cross-functional teams Proven ability to take independent action to initiate process improvements when needed Proven ability to work in a matrix-like manner where cross-functional interaction is an implicit way of working Solid time-management skills to meet deliverables commensurate with a fast-paced environment Well organized, able to multitask and prioritize competing tasks Ability to use SAS at the expert level Experience with small biotech companies and high paced work environment is a plus A strong understanding of clinical trial data including ability to prepare simple listings, pivot tables and reports using SAS to assist in data review Excellent organizational skills with ability to manage staff, projects and resources to meet timelines and budgets Effective problem solving, collaboration and strong teamwork skills Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment Able to manage expectations with supervisors, peers and customers Amount of travel: Currently up to 5% Associated topics: data center, data integration, data integrity, data quality, data scientist, data warehouse, database, erp, hbase, mongo database administrator

Looking for Senior Core Java Developer a long term contract. South San Francisco, CA (Must be local candidates) Need someone with hands on: Core Java Development (Strong in Back-end development) 12-15 years IT experience. SQL JPA OR Spring Strong in performance tuning AWS (Certification nice to have) ****Interested candidates can apply resumes at ...@veear.com or can call at 415-###-####**** - provided by Dice Associated topics: .net, algorithm, backend, back end, c c++, c++, developer, java, sdet, sw

We are looking for software engineers to join the Bioinformatics team at Myriad Womens Health and help build the analytical pipeline responsible for delivering meaningful health impact to hundreds of thousands of patients a year. The ideal candidate will enjoy working in a collaborative, multidisciplinary R&D environment as we build innovative solutions for bioinformatics software systems. They will have a scientific curiosity with eagerness to learn and explore new challenges since their work will enable breakthroughs in genomics. WHAT YOU'LL DO + Lead, design, and architect major bioinformatics initiatives to expand the capabilities of bioinformatics ecosystem + Author innovative, robust, and high quality software systems + Responsible for core NGS products analytical pipeline from raw sequencing data to patient genotypes + Build frameworks and practices to enable continuous integration for science + Industry thought leadership with contributions to open source bioinformatics tools + Build frameworks and applications to support simultaneously running projects at scale ABOUT YOU + Deep thinker about systems and how systems should work optimally + BS/MS/PhD in Computer Science or related computational science (previous genetics experience not required!) + 5+ years industry experience with demonstrated project leadership + Proven track record of developing innovative and high performance bioinformatics algorithms and analysis pipelines + Full-stack capability; proficient in scientific Python 3 (numpy, scipy, pandas, scikit learn, etc) + Fluency with Linux, high-performance computing clusters, shell scripting, databases, and analysis pipelines. Bonus for background in cloud computing architecture + Experience with (or eagerness to learn) modern genetics tools + Previous experience in regulated clinical environment with rigorous design control and software validation a big plus + Experience with large scale data science, statistical modeling, and machine learning a plus Requisition ID: 2019-9379 Name: Myriad Genetics, Inc. External Company Name: Myriad Genetics Inc. External Company URL: www.myriad.com Street: 180 Kimball Way Associated topics: .net, application architect, application developer, architect, back end, c/c++, develop, project architect, software architect, software engineer lead

Job Description Join Hired and find your dream job as a Senior Full-Stack Software Engineer at one of 10,000+ companies looking for candidates just like Associated topics: algorithm, application, c++, c#, develop, devops, programming, python, sde, sw

The Position: Veracyte, Inc. is a leading genomic diagnostics company that is fundamentally improving patient care by resolving diagnostic uncertainty with evidence that is trustworthy and actionable. The company's products uniquely combine genomic technology, clinical science and machine learning to provide answers that give physicians and patients a clear path forward without risky, costly surgery that is often unnecessary. Based on our company s outstanding success with our first commercial solutions along with our rich product pipeline, we are aggressively investing in our Software development and testing team. As a lead software test engineer, you ll make an immediate impact by managing and leading the testing process for applications at Veracyte that directly help our company expand and develop new diagnostic solutions to improve patient outcomes and lower healthcare costs. You'll report to our Senior Director of Software Development and as a core member of the team you'll lead testing of mission critical systems and applications for commercial, lab and clinical systems at Veracyte. In this role, you'll have ownership of QA and testing of high impact solutions for both web and mobile platforms in a distributed micro services environment. You will be collaborating with all stake holders including business leaders, end users and teammates. This is an opportunity to use industry standard best practices and state of the art technologies to plan, execute and manage testing lifecycle. Additionally, this is an opportunity to increase the efficiency of testing by test automation. Who You Are: Experienced leading and executing across all aspects of quality assurance including establishing metrics, applying industry best practices, and developing new tools and processes to ensure quality goals are met. Acted as key point of contact for all testing and QA aspects of releases, providing testing services and coordinating resources internally and externally. Developed and executed test cases, scripts, plans and procedures (manual and automated) Demonstrated strong analytical skills coupled with the ability to find and solve the root cause of problems. Excellent critical thinking and troubleshooting skills. Strong collaboration skills with end-users and development team. Excellent written and spoken communication skills 5+ years of experience in the software test and QA field. 2+ years of experience establishing and leading formal QA processes, ensuring that the team is using industry-accepted best practices What 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 work collaboratively, offering you the opportunity to constantly learn from your colleagues even those outside of your area of expertise. Here at Veracyte, we find fun, little ways to make it a great place to work participate in our annual Halloween costume contest, treat yourself to free coffee or the endless supply of PB&J sandwiches, and a toast with colleagues as we celebrate milestones. We are a company with a heart and believe in positively impacting the world beyond our doors by providing our product to those who cannot afford it through a financial assistance program. Veracyte seeks the best employees and works to create an environment where they can thrive, expand their knowledge and contribute at the highest level. About Veracyte Veracyte, Inc. is a leading genomic diagnostics company that is fundamentally improving patient care by resolving diagnostic uncertainty with evidence that is trustworthy and actionable. The Company s products uniquely combine genomic technology, clinical science and machine learning to provide answers that give physicians and patients a clear path forward without risky, costly surgery that is often unnecessary. Since its founding in 2008, Veracyte has commercialized three genomic tests, which are transforming the diagnosis of thyroid cancer, lung cancer and idiopathic pulmonary fibrosis and collectively target a $2 billion market opportunity. At Veracyte, we are more than just a diagnostics company. We are redefining diagnostic truth and changing patient care as we know it. We are improving the lives of patients by enabling the evolution of evidence-based clarity from scientific discovery. Our team embraces challenges - the more complex, the better. We are laser-focused and know how to prioritize. We act with a sense of urgency, because when it comes to advancing patient care, every minute matters. We take ownership of our work and are deeply committed to the success of our team. And, above all, we value integrity - in our work and how we treat all of our stakeholders, including each other. Our accomplishments and innovation have earned us widespread recognition, from appearing on The Wall Street Journal Next Big Thing list to receiving the 2016 Edison Award, which honors product innovation and excellence. Yet the honor we are proudest of is being named a Top Workplace by the Bay Area News group four years in a row, based solely on feedback from our employees. Veracyte affords equal employment opportunities to all qualified persons, regardless of race, color, religion, national origin, age, sex, disability, sexual orientation, gender expression, veteran or marital status. Veracyte participates in E-Verify in the United States Associated topics: automation, performance test, process, quality, quality assurance, quality assurance engineer, quality assurance lead, software quality, software quality assurance, tester