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Job DescriptionThe AV Safety Software Data Engineer will play a critical role in supporting Zoox’s safety data reporting and compliance efforts. In this position, you will work with large-scale fleet data to gather, analyze, and triage events for internal safety learnings and external compliance requirements. As an AV Safety Software Data Reporting Engineer, you will operationalize defined requirements through data-driven analyses, dashboards, and workflow automations. You will implement innovative processes that are rigorous, diligent, and systematic, as well as applicable and repeatable, as Zoox continues to scale, to ensure reliable and safe operations. You will continually improve our internal data-gathering, analysis, and reporting processes and work closely with our Legal, Policy, Operations, Vehicle Engineering, Safety Design, Software, Hardware, and Communications teams to ensure a rigorous, disciplined, quantified engineering approach. A successful candidate will be able to support other Zoox safety efforts, including Operational Safety, Safety Planning, Policy, System Design, and Risk Assessment activities.In this role, you will: • Create, implement, and maintain our internal and external safety data gathering, analysis, and reporting processes, and work cross-functionally with other internal organizations to ensure accurate regulatory reporting., • Support the implementation of safety learnings & data programs, processes and dashboards for awareness and decision-making, including systematically ensuring representation and input from key internal stakeholders., • Continuously improve data pipelines, triage processes, and dashboard functionality to support efficient safety data reporting., • Leverage AI tools (LLMs/VLMs, prompt engineering, and context engineering) to assist with event summarization, semi-automated triage, and workflow automation., • Support the continuing development and implementation of successful operational safety and compliance programs., • Design, build, and maintain dashboards in Looker and Databricks to track safety data reports, learnings, and feature implementation.Qualifications, • BS or MS in Computer Science, Data Science, Robotics, Statistics, or a related field., • 4+ years of experience working with large-scale datasets, preferably in autonomous vehicles, robotics, or other safety-critical systems., • Strong programming skills in Python (pandas, PySpark) and advanced SQL/Spark query development., • Experience designing and maintaining dashboards in Looker, Databricks, Tableau, or similar platforms., • Demonstrated attention to detail in analyzing technical, engineering or forensic data., • Familiarity with AI tools (LLMs/VLMs, prompt engineering, context engineering) for data analysis, triage, or workflow automation., • Experience working with cross-functional teams and communicating technical content clearly to both engineering and non-technical audiences.Bonus Qualifications, • Experience with NHTSA SGO, TREAD, or State AV reporting requirements, • Experience in automated vehicle systems or diagnostic data or large-scale fleet data, • Understanding of AV stack components and vehicle behavior, • Advanced degree in Engineering, or in a technical field, • Certification in Safety or Automotive systemsBase Salary Range There are three major components to compensation for this position: salary, Amazon Restricted Stock Units (RSUs), and Zoox Stock Appreciation Rights. A sign-on bonus may be offered as part of the compensation package. The listed range applies only to the base salary. Compensation will vary based on geographic location and level. Leveling, as well as positioning within a level, is determined by a range of factors, including, but not limited to, a candidate's relevant years of experience, domain knowledge, and interview performance. The salary range listed in this posting is representative of the range of levels Zoox is considering for this position. Zoox also offers a comprehensive package of benefits, including paid time off (e.g. sick leave, vacation, bereavement), unpaid time off, Zoox Stock Appreciation Rights, Amazon RSUs, health insurance, long-term care insurance, long-term and short-term disability insurance, and life insurance.About ZooxZoox is developing the first ground-up, fully autonomous vehicle fleet and the supporting ecosystem required to bring this technology to market. Sitting at the intersection of robotics, machine learning, and design, Zoox aims to provide the next generation of mobility-as-a-service in urban environments. We’re looking for top talent that shares our passion and wants to be part of a fast-moving and highly execution-oriented team. Follow us on LinkedIn AccommodationsIf you need an accommodation to participate in the application or interview process please reach out to accommodations@zoox.com or your assigned recruiter. A Final Note:You do not need to match every listed expectation to apply for this position. Here at Zoox, we know that diverse perspectives foster the innovation we need to be successful, and we are committed to building a team that encompasses a variety of backgrounds, experiences, and skills. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job DescriptionSUMMARY: Individual will be involved in writing and creating some technical knowledge base articles, etc. REQUIREMENTS: • Solid analytical and content management skills., • Creating and updating technical knowledge bases

Job Description Description We are seeking a Technical Writer to support GMP documentation activities in a biotech environment. This role will focus on creating, editing, and maintaining compliant documentation across supply chain, inventory management, manufacturing, and clinical supply operations. The Technical Writer will collaborate cross-functionally with Quality, Manufacturing, and Supply Chain teams to ensure accuracy and regulatory compliance. Skills gmp, technical writing, supply chain, sop, forms, inventory, inventory management, biotech, erp system, mrp system, electronic document management system edms, clinical trial supplies Top Skills Details gmp,technical writing,supply chain,sop,forms,inventory Additional Skills & Qualifications Bachelor’s degree or equivalent experience in Life Sciences, Supply Chain, or related field 5+ years of technical writing experience in biotech, pharmaceutical, or regulated industry Strong GMP documentation experience required Familiarity with supply chain, warehouse, and clinical supply processes Strong organizational, communication, and attention-to-detail skills Experience Level Intermediate Level Job Type & Location This is a Contract position based out of South San Francisco, CA. Pay and Benefits The pay range for this position is $35.00 - $55.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in South San Francisco,CA. Application Deadline This position is anticipated to close on Jul 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionBenefits: • Free uniforms, • Opportunity for advancement, • Paid time off, • Training & development, • Vision insurance, • 401(k) matching, • Dental insurance, • Employee discounts BIG O TIRES has immediate opportunities for experienced service advisors and customer service professionals and are interviewing proven TEAM MEMBER candidates today for our Service Centers If you have proven Auto Repair Advisor/Tire sales experience, and if you strive to be the best....we would like to talk with you. The right candidate has a proven sales drive to meet our customer's automotive needs.. What we're looking for: • Demonstrated Tire / Service sales experience., • Excellent communication, or organizational and written skills, • Customer oriented and able for responding to customer concerns and and repair concerns., • Achieving sales goals and budgets while maximizing profitability, • Knowledge of Brakes, Suspension, Ride Control, Tune ups, Alignments, Tires and More.What BIG O Offers:, • Excellent compensation based on proven experience. Our compensation includes a Commission Plan for Advisors, • Great Family Health, Vision, Dental Insurance Plan Commission and Spiff Program., • 5 Day work week (Opened 6 Days a Week), • Paid Vacations / Paid Holidays, • Online Training Program, • 401K Plan, • Employee Referral Program, • Uniforms Provided, • Opportunities for AdvancementWe will provide the tools, training and resources to help you succeed. We are an Equal Opportunity Employer with a benefits package that includes: Excellent pay w/incentives Health Insurance (Medical/Dental/Vision) Paid vacation Uniforms Paid Employee Purchase Program Contact Bill Moseley at bill.moseley@bigo.com for immediate consideration and to discuss next steps. Take the BIG O TIRE challenge today !! We are an equal opportunity employer, dedicated to a policy of non-discrimination in employment on any basis including race, creed, color, age, sex, religion or national origin. We are committed to building a culturally diverse faculty.

Job DescriptionSenior Scientist, Translational Immunology Location: South San Francisco, CA (On-site) Parvus Therapeutics Inc. Parvus Therapeutics Inc. is a privately held biopharmaceutical company developing Navacims™, a platform technology based on foundational research published in 2016 (Nature 530:434), to treat autoimmune diseases. Parvus’ mission is to shift the treatment paradigm toward Navacim™-directed immune regulation, avoiding non-specific immune suppression associated with current therapies. Parvus’ innovative approach has the potential to benefit millions of patients suffering from debilitating autoimmune diseases and other chronic inflammatory conditions. Parvus is advancing a pipeline of proprietary drug candidates for multiple autoimmune indications through preclinical development and into the clinic. Parvus’ leadership team is experienced in successful drug discovery, development, manufacturing, regulatory approval, and commercialization. The Position We are seeking a Senior Scientist to join our team and drive projects enabling the translation, validation, and execution of preclinical biomarkers to the clinic. Primary Responsibilities: • Identify and validate biomarkers relevant to the pharmacology of target clinical candidates., • Lead context-of-use validation (in-house or through CLIA-certified laboratories or clinical CROs) of clinical biomarker assays suitable for use in recommended phase 2 dosing selection and/or regulatory submission., • Write and amend internal SOPs and reports as necessary for GSP or GCLP purposes., • Liaise with nonclinical pharmacology and discovery immunology teams to establish proof-of-concept/proof-of-mechanism biomarker strategies suitable for use in NHPs and FIH studies., • Participate in all aspects of lab operation, training, and compliance including external audits where applicable., • Other duties and responsibilities as assigned.Requirements:, • Bachelors degree with a minimum 10 years of experience or a Masters degree with a minimum of 6 years of experience (at least 2 years must be in biotech or industry setting) in Immunology or other relevant life sciences. Experience with regulatory T cells or Tr1 cells will be prioritized., • Expertise in high-dimensional flow cytometry assays including but not limited to spectral flow cytometry and CyTOF., • Experience leading phase appropriate clinical bioanalytical assay development and analyses including full validation and management of clinical bioanalytical labs/CROs., • Experience developing lean and agile clinical biomarker budgets suitable for early phase POC and POM studies., • Nice to have:, • Experience with nanomedicine, • Experience with IQOQ, • Familiarity with biomarker-centric platforms such as spatial profiling, multi-omics integration, • Excellent oral, written communication, and presentation skills., • Demonstrated ability to effectively work in cross-functional teams, meet deadlines, and prioritize multiple projects is required., • Comfortable working collaboratively in a small, fast-paced environment., • Ability to quickly adjust to shifting project demands and priorities.The expected annual salary range for this role is $150,000 – $170,000. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. Powered by JazzHR pZpcx9xnpv

Job Description "All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment". Job Title: Senior Medical Content Writer Location: South San Francisco, CA Duration: 03 Months Contract Pay Rate: $68/hr Notes: • Working Model (hybrid, remote, fully onsite): Hybrid (Tue-Wed-Thu in office), • Working days: Monday through Friday, • Working hours (e.g. 8 AM to 4 PM PT, 9 AM to 5 PM, etc.): 8am to 4pm, • Interview Format (e.g. one round, two rounds, and length of interviews [30, 45, 60, 90 minutes]): Two interviews, 45 minutes each. About the Role: • We are looking for a Senior Medical Content Writer who can do the hardest kind of writing in pharma: claims. You will develop, substantiate, and annotate promotional and educational claims, and write the medical content that carries them & mdash; accurately, clearly, and in a way that survives MLR review without losing its edge. You will work embedded in an in-house creative studio, alongside creative directors and designers, which means your writing needs to work as creative material, not just as reference text. What You'll Do: • Draft, refine, and substantiate promotional and non-promotional claims grounded in clinical data, prescribing information, and peer-reviewed literature., • Build annotated references and claim substantiation packages ready for MLR submission., • Write medical content across formats: HCP materials, patient education, disease-state content, congress panels, digital assets, video scripts, and sales materials., • Ensure fair balance, accurate ISI integration, and on-label alignment in all promotional content., • Partner with medical affairs and regulatory reviewers to resolve claim language efficiently; anticipate objections and offer compliant alternatives proactively., • Collaborate with creative directors and designers so that copy and visual concepts develop together rather than sequentially., • Maintain claim libraries and reference databases to accelerate reuse across the portfolio. What You Bring: • 5 - 8 years of medical writing experience in pharma, biotech, or a medical communications agency, with direct experience writing and substantiating claims., • Deep familiarity with the MLR review process and what makes claims approvable: substantiation standards, referencing conventions, and common reviewer objections., • Strong command of AMA style and the ability to read and accurately interpret clinical trial data, publications, and prescribing information., • Understanding of FDA/OPDP promotional regulations, fair balance requirements, and ISI standards., • Range as a writer: able to move between rigorous scientific accuracy and accessible, engaging language for different audiences (HCP, patient, internal)., • Meticulous attention to detail in referencing, annotation, and version control. Nice to Have: • Advanced degree in life sciences (PharmD, PhD, MS) or equivalent scientific depth., • Experience with Veeva Vault Promo Mats annotation workflows., • Oncology, immunology, or biologics therapeutic area experience., • Experience working inside an in-house studio or embedded content team. About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

Job Description Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date. We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team. We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment. For more information see: www.septerna.com. THE ROLE This is a contracted position requiring 20-30 hours per week for a 6-month term. The Veterinary Technician / Research Associate will initially be responsible for conducting in vivo rodent studies, with the potential to engage in additional ex vivo or in vitro studies in the Translational Sciences Department to support the advancement of Septerna's small molecule drug discovery pipeline. The candidate will work independently and collaboratively in an inter-disciplinary setting to execute experiments in preclinical models to understand in vivo pharmacology, establish PK/PD relationships, and inform the efficacy of Septerna's therapeutic candidates. They will help generate in vivo and/or ex vivo data to determine therapeutic mechanisms of action, in vivo efficacy, and rank candidates for preclinical development. This role is expected to be primarily in the lab with some desk work. Regular weekend working hours will be required. We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will help move therapies through preclinical development, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team on the frontlines of innovative therapeutic development. The position is based in South San Francisco, CA. Key Responsibilities include but are not limited to: • Execute in vivo pharmacology studies to understand therapeutic mechanisms in relevant disease models, • Work collaboratively to determine the mechanism of action of drug candidates, primarily with in vivo models, • Be a member of multiple project teams, • Dose large volumes of animals (approx. 50-80 rats per day), • Maintain and organize lab spaces, • Follow all company policies/practices, and maintain accurate records and notebooks, • Perform routine weekend study activities REQUIRED EDUCATION, SKILLS & EXPERIENCE • At least 2 years direct full-time experience with in vivo studies in academia or the biotechnology and pharmaceutical industries, • Experience working in vivarium laboratory settings with rats, • Demonstrated ability to be hands on and work directly with rodent models, including multiple routes of administration (e.g. oral, subcutaneous, intraperitoneal, intravenous, intramuscular) and sample collection (e.g. tail vein bleeds, jugular bleeds, cardiac puncture, necropsies, etc.)., • Experience working with other scientists to collect and record study data consistently and accurately, • Ability to collaborate and trouble-shoot biological experiments, • Detail-oriented and organized, with strong interpersonal skills for clear and effective communication – ability to proactively engage and collaboration with colleagues PREFERRED SKILLS & EXPERIENCE • BSc in Pharmacology, Toxicology, Animal Science, or related biological science, • Experience working with in vitro/ex vivo protein and RNA/DNA assays (e.g. ELISA, qPCR), • Experience with subcutaneous injections and oral gavage routes of administration, • Experience collecting and processing blood samples, especially timed blood collections, • Experience with cell culture, • Experience with data analysis using Excel and/or Prism, • Experience working with rodent surgical models, • Previous work on therapeutic discovery and development programs in the field of endocrine, inflammatory, neuroscience, or metabolic diseases The anticipated salary range for candidates who will work in South San Francisco, CA is $30.00/hr - $40.00/hr. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are 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. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Job DescriptionOverview We are seeking a Technical Writer to join its Global Product Team. This role is responsible for creating, maintaining, and publishing high-quality internal and client-facing documentation that supports product integrations, implementation activities, and ongoing customer success. The ideal candidate combines strong technical writing expertise with project management skills and the ability to translate complex technical concepts into clear, user-friendly content. Experience leveraging AI tools for content development and documentation management is highly valued. Key Responsibilities • Create, edit, and maintain comprehensive technical documentation, including:, • Implementation Guides, • Program Guides, • Technical Reference Documentation, • Best Practices, • FAQs, • Technical Specifications, • Supporting Product Materials, • Partner closely with Product Managers, Engineers, and cross-functional stakeholders to understand technical requirements and translate them into clear, accurate, and customer-friendly documentation., • Ensure all published content adheres to documentation standards, style guidelines, and quality assurance processes., • Own the end-to-end documentation lifecycle, including intake, drafting, review, approvals, publication, and maintenance., • Prioritize and manage documentation requests through JIRA, coordinating timelines and deliverables across multiple projects., • Establish and facilitate documentation intake, review, and publishing cadences with global product stakeholders., • Maintain documentation inventories, version control records, publication logs, and working drafts., • Develop and manage capacity planning workbooks to track project milestones, publication schedules, service-level agreements (SLAs), and business priorities., • Utilize AI tools such as OpenAI, Claude, and similar platforms for content drafting, quality reviews, style consistency, and process optimization., • Drive stakeholder accountability by coordinating content reviews, tracking deliverables, managing deadlines, and facilitating alignment meetings., • Support publication and distribution of documentation to internal and external repositories.Required Qualifications, • 3–5 years of experience in Technical Writing, preferably supporting client-facing products, technical integrations, or software documentation., • Proven experience developing documentation for technical audiences such as developers, fraud analysts, payment professionals, or similar stakeholders., • Exceptional written communication, editing, and proofreading skills with strong attention to detail., • Experience creating Standard Operating Procedures (SOPs), implementation guides, and technical documentation., • Familiarity with AI-powered content creation and automation tools., • Strong project management and organizational skills with the ability to manage multiple priorities and deadlines., • Excellent communication, collaboration, and stakeholder management abilities.Required Skills, • Technical Writing, • SOP Development, • AI Tools (OpenAI, Claude, etc.), • Product Documentation, • Project Management, • Content Editing & Review, • Stakeholder Management, • JIRA Job Type & Location This is a Contract to Hire position based out of Foster City, CA. Pay and Benefits The pay range for this position is $35.00 - $40.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Foster City,CA. Application Deadline This position is anticipated to close on Aug 10, 2026. About Aston Carter Aston Carter provides world-class corporate talent solutions to thousands of clients across the globe. Specialized in accounting, finance, human resources, talent acquisition, procurement, supply chain and select administrative professions, we extend the capabilities of industry-leading companies. We draw on our deep recruiting expertise and expansive network to meet the evolving needs of our clients and talent community with agility and excellence. With offices across the U.S., Canada, Asia Pacific and Europe, Aston Carter serves many of the Fortune 500. We are proud to be a ClearlyRated Best of Staffing® Platinum Award winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email astoncarteraccommodation@astoncarter.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description We are looking for a strategic and hands-on leader to bridge the gap between early discovery and our patients. As the Senior Director of Translational Research & Biomarkers, you will design and execute the translational strategies to support the development of our clinical portfolio. You’ll lead efforts developing and identifying the biomarkers that help identify how to select our patients and to demonstrate that our molecules impact the desired target biology. Key Responsibilities • Strategic Leadership: Develop and lead the overarching translational medicine strategy for the entire pipeline, from lead optimization to Phase II/III., • Biomarker Discovery: Oversee the identification, development, and validation of pharmacodynamic, predictive, and prognostic biomarkers., • Clinical Integration: Collaborate with Clinical Development to integrate biomarker assays into clinical protocols and ensure high-quality data collection and analysis., • Cross-Functional Partnership: Act as the primary link between Discovery Research, Clinical, and Regulatory Affairs to ensure seamless program transitions., • External Innovation: Manage relationships with CROs, academic collaborators, and potential diagnostic partners for assay development and companion diagnostic (CDx) strategies., • Regulatory Representation: Lead the translational/biomarker sections of regulatory filings (IND, CTA, BLA/NDA) and represent the company in meetings with health authorities (FDA/EMA).Qualifications, • Education: PhD or MD in Biology, Pharmacology, Oncology, Immunology, or a related field., • Experience: 10+ years in the biopharma industry, with a proven track record of moving programs from bench to bedside., • Technical Expertise: Deep knowledge of diverse platform technologies (e.g., NGS, IHC, flow cytometry, proteomics, liquid biopsy)., • Strategic Mindset: Experience developing validated lab tests/Cdx and a strong understanding of global regulatory requirements for biomarkers., • Leadership: A history of managing high-performing teams and influencing stakeholders in a fast-paced, matrixed environment.About Attovia Attovia is creating a pipeline of biotherapeutics with initial focus immune-mediated disease. The company leverages Attobody™, a novel biologics platform, to generate small format biparatopic binders that expand the addressable target universe across disease areas and can offer stronger efficacy, faster speed to response, and an improved safety profile than traditional approaches. We are currently progressing multiple programs across immune-mediated disease indications. Our culture is centered around five core pillars: • Integrity, • Learning & Growth, • Drive for Excellence, • Innovation, • Teamwork & Collaboration We take pride in fostering a strong team and dynamic work environment, and we are seeking individuals who align with our values and contribute to a positive and impactful workplace. Attovia is located in San Carlos, CA. Attovia is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Learn more about Attovia: www.attovia.com Leveling and salary is commensurate with experience. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job Description POSITION SUMMARY: Focus Interpreting is seeking a skilled Spanish Consecutive Interpreter to join our team in San Mateo, CA. In this role, you will provide accurate and professional interpretation services to facilitate communication for Spanish-speaking individuals in various environments. RESPONSIBILITIES: • Render accurate consecutive interpretation services during meetings, interviews, medical appointments, and other communications involving Spanish and English speakers., • Ensure the clarity and integrity of the message interpreted while adhering to professional and ethical standards., • Maintain confidentiality and professionalism throughout all assignments., • Prepare for assignments by researching relevant terminology and understanding the specific needs of clients., • Continuously enhance language skills and subject matter knowledge to improve service delivery. REQUIREMENTS: • Fluency in both Spanish and English, with outstanding oral and written communication abilities in both languages., • Strong understanding of cultural nuances to facilitate effective communication., • Excellent listening and analytical skills to ensure precise interpretation., • Prior experience in consecutive interpretation is preferred. If you are an experienced interpreter looking to join a supportive team and contribute to effective communication for the Spanish-speaking community, we invite you to apply! Requirements • Fluency in Spanish and English, • Strong communication skills, • Knowledge of cultural nuances, • Excellent analytical skills, • Prior experience in consecutive interpretation preferred Benefits Paid per assignment per hour

Job Description Join the XRG Team: Where Passion for Hospitality Meets Limitless Opportunities! At Xperience Restaurant Group (XRG), our foundation is built on the unwavering dedication of team members who exude a relentless passion for hospitality. We have set our standards high, never settling for anything less than the extraordinary, because at XRG, we believe in delivering not just meals but unforgettable eXperiences. If you're one of those individuals, we invite you to join our XRG Team! Why XRG? Here's a Taste of What We Offer: • Competitive pay: Your hard work deserves more than just a paycheck. Enjoy competitive pay that recognizes your dedication and skills., • Flexibility: Strike the perfect balance between work and life with our flexible hours. Your time matters, and we value your well-being., • Career Growth Opportunities: We thrive on promoting from within, fostering #XperienceRealGrowth for every team member., • Unique Culture: Our Core Values set us apart, making the XRG culture truly unmatched. Join the #XRGFam and eXperience the difference., • Team Member Dining Discounts: Savor the perks of being part of our team with exclusive dining discounts for you and up to 5 guests., • Employee Referral Program: Share the joy of being part of the XRG team with others., • Financial Well-Being: Exclusive Credit Union Benefits, including Checking/Savings, Loans, and Financial Education., • Partner Perks: Unlock discounted rates on theme parks, travel, apparel, sports tickets, and more!, • Sick Time: Offered in eligible states (CA, CO, AZ, MA, MD, WA, NY, NV, IL), we've got you covered!, • Health Insurance: Take care of your well-being with comprehensive health insurance for our full-time team members. Join XRG, where every team member is a valued part of our journey. Discover a workplace that goes beyond expectations, a place where your passion meets endless possibilities. Certified Top Workplaces- 7 years running! Compensation Range: $18.15- $18.65/Hour *Range(s) - DOE PURPOSE Food Expeditors arrange the transfer of food from the kitchen line to the serving floor. They ensure each plate is prepared neatly, properly and in accordance with customer specifications, such as well-done or with extra cheese. Expeditors prepare condiments and side dishes for each order, verify product temperatures and alert servers when orders are ready to go. In some establishments, such as bar and grills, they might deliver food to the bar rather than calling on servers. DUTIES & RESPONSABILITIES • Responsible for helping to maintain the efficiency of a restaurant kitchen by delivering dishes to the table, • Making sure to deliver items to the customer’s table when they are ready., • Assists waiters and waitresses., • Keeps up a constant flow of items from the kitchen to the table to the dishwasher. QUALIFICATIONS & SKILLS • Ability to stay organized throughout the day to avoid becoming overwhelmed during busy times., • Must also be able to communicate well with other members of restaurant staff., • Needs to be coordinated and able to keep track of several different tasks at once., • It’s important that an expeditor is not afraid to speak up loudly to let coworkers know what needs to be done., • Excellent communication skills., • Effective verbal and written communication skills WORKING CONDITIONS The working conditions described below are representative of those a team member encounters while performing the essential duties and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties and responsibilities of this job. • Work indoors and/or outdoors, exposed to hot and/or cold surfaces, steam, and wet floors, • Work in an environment that is subject to varying levels of noise, crowds and smoke, the severity of which depends upon guest volume, • Fast paced, high volume, full service restaurant, • Work varied shifts to include days, nights, weekends and holidays PHYSICAL REQUIREMENTS The physical demands described below are representative of those that must be met by a team member to successfully perform the essential duties and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions. • Ability to walk long periods of time, • Ability to stand for long periods of time, • Ability to use hands to handle, control, or feel objects, tools, or controls., • Ability to repeat the same movements for long periods of time, • Ability to understand the speech of another person, • Ability to speak clearly so listeners can understand, • Ability to push and lift up to 50 lbs, • Ability to reach with hands and arms; climb stairs; balance; stoop, kneel, crouch or crawl DISCLAIMER This job description is a summary of duties, which you as a Food Expeditor are expected to perform in your normal course of work. It is by no means an all-inclusive list but is merely a broad guide of expected duties. You should understand that a job description is neither complete nor permanent; it can be modified at any time with or without notice.

Job Description POSITION SUMMARY: Focus Interpreting is seeking a talented Spanish Simultaneous Interpreter to join our team in San Francisco, CA. This role is essential for providing high-quality, real-time interpretation services during conferences, meetings, and events, ensuring seamless communication between Spanish-speaking participants and English speakers. RESPONSIBILITIES: • Deliver simultaneous interpretation services at various events, allowing Spanish and English speakers to communicate effectively., • Utilize interpretation equipment and advanced technology to ensure clear and accurate communication., • Maintain a high level of professionalism and confidentiality during all interpretation sessions., • Prepare for assignments by familiarizing yourself with relevant terminology and the specific context of the event., • Continuously refine your language skills and knowledge of industry-specific vocabulary to enhance interpretation accuracy. REQUIREMENTS: • Fluency in both Spanish and English, with excellent oral and written communication skills., • Demonstrated experience in simultaneous interpretation, with a solid understanding of its techniques and challenges., • Strong awareness of cultural nuances to convey meanings accurately and sensitively., • Exceptional listening abilities and cognitive skills to process and interpret information in real-time., • Previous experience working in a professional interpreting environment is preferred. If you are a dedicated and skilled simultaneous interpreter looking to make a significant impact in San Francisco, we would love to connect with you! Requirements • Fluency in Spanish and English, • Demonstrated experience in simultaneous interpretation, • Strong communication skills, • Knowledge of cultural differences, • Exceptional listening and cognitive skills, • Previous professional interpreting experience preferred Benefits Paid per assignment per hour.

Care Coordinator Medical Interpreter Burlingame, CA 94010 Overview Salary Range $36.92 - $41.85 Hourly Description Summary Of Position: The Care Coordinator Medical Interpreter is part of the NEMS MSO Care Coordination and Case Management (CC/CM) team. The primary function of the Care Coordination Medical Interpreter is to establish communication between health care providers and NEMS patients who have limited English proficiency or prefer to speak in their native tongue. The interpreter's responsibility will be to interpret and to translate complex medical information to patients and ensure there is complete understanding of medical information between doctors, nurses, medical staffs, and patients. This position is required to provide service over virtual systems as well as provide face-to-face service at various types of medical facilities, e.g. physician offices, hospital outpatient facilities, nursing homes, rehabilitation centers, etc. This position is an important communication link between doctors and patients. Candidate is required to have effective communication skills and knowledge to avoid cultural misunderstandings between patients and medical professionals, strive to provide a positive and relaxed experience so patients feel comfortable disclosing sensitive information about their medical conditions. While serving to bridge the language barrier between patients and doctors, this position must uphold patient confidentiality in accordance with policies and procedures of NEMS and other medical facilities. The Care Coordinator Medical Interpreter is required to have well-understanding of the many benefits and coverage offered by the different managed care products, including Medicare Advantage, D-SNP, Medi-Cal Managed Care, and other Supplemental programs. In order to ensure eligible patients are receiving timely and efficient health care and support services, the Care Coordinator Medical Interpreter will also be responsible to facilitate medical, behavioral, social and community support services for patients in need of enhanced care coordination services. These services will be through the development of a multi-disciplinary care plan, self-management goals and referrals to both internal and external resources. Essential Job Functions: Accompany non-English speaking patients to specialist medical appointments or provide service virtually; establish effective communication between doctors, nurses and patients at the medical appointment by interpreting and translating a wide range of medical information that includes medical conditions, treatment options, follow-up appointment details, insurance coverage, etc., at the medical care facility Translate medical documents such as medical history questionnaire, post-appointment/discharge summary, self-care instruction, health education lecture materials, etc. for patients prior to, during, and after medical appointments. Assist patients with understanding and completing paperwork that's required for medical procedure(s) Provide accurate interpretation of communication between patient and healthcare providers; ensure the understanding of information exchange between the parties involved. Connect through various virtual systems to deliver service. Coordinate care for patients after the medical appointment to ensure referrals to other specialist(s) and/or medical procedure(s) are in place Monitor delivery of care by identifying progress toward desired care outcomes; interact with involved services providers and/or facilities to negotiate and expedite scheduling and completion of tests, procedures, and consults Participate in interdisciplinary care team meetings to evaluate outcomes of care by measuring intervention effectiveness; implements team recommendations Be the system navigator and point of contact for patients enrolled in managed care programs, assist patients with benefit coverage and access to care questions/concerns Provide enhanced care coordination services assisting patients in problem solving with issues related to the health care system, financial or social barriers Conduct outreach activities to assigned members by phone, mail or any other forms of communication method to promote program engagement and NEMS marketing strategy Collect and report statistical information for monthly and quarterly reports Document program measure results and submit to MSO Committee as needed Contribute to NEMS' marketing strategy and other outreach project planning Performs other job duties as required by manager/supervisor Qualifications Completion of a two-year degree from an accredited higher education institution Certification from an accredited Medical Interpreter program or Healthcare Interpreter Program in Cantonese and/or Mandarin, Vietnamese, or Spanish. May be substituted by passing the LanguageLine Interpreter Skills Test (IST). 1-3 years' experience interpreting in a clinical setting preferred Strong knowledge of medical terminology. Excellent listening, speaking, and retention skills to accurately convey messaging Excellent social, communication skills, strong analytical, and problem-solving skills Valid driver's license and ability to operate company vehicle Knowledge of State/Federal healthcare compliance requirements, particularly DHCS/Medi-Cal guidelines a plus Ability to self-manage in a detail-oriented environment Ability to operate PC based software programs or automated database management systems Good organization and prioritization skills, outstanding in time management Language: Must be able to fluently read, write, and speak English Must be verbally fluent in the foreign language that's required for the position. The ability to speak an additional foreign language is a plus. Status: This is an FLSA Non-exempt position. This is not an OSHA high-risk position. This is a Full Time position. NEMS is proud to be an Equal Opportunity Employer welcoming diversity in our workforce. Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. NEMS BENEFITS: Competitive benefits, including free medical, dental and vision insurance for employee, spouse and/or children; and company contribution to 401(k).

Job Location: Foster City CA 94404.PMO Documentation Lead & Technical Writer.The Program Management Office (PMO) at supports some of the company's most complex, cross-functional decisions and programs.When needed, members of the PMO will roll up their sleeves and work hand in hand with engineering a

You will work with cross-functional teams (eg, Regulatory Affairs, Clinical Research, Clinical Operations, Clinical Pharmacology, Patient Safety, and Clinical Data Science) to deliver documents on time and per team expectations and drive document strategy for Medical Writing. Participates in develop

Partner with Quality Assurance to establish and update SOPs supporting medical writing activities. Associate Director Medical Writing. We are seeking an Associate Director, Medical Writing to lead the development and execution of high-quality clinical and regulatory documentation.

Vaxcyte is seeking a Director, Clinical Medical Writing to drive and shape the medical writing processes, procedures, strategies, and document generation and maintenance. The Director, Clinical Medical Writing will develop new SOPs and templates and contribute towards existing SOPs to support the wr

Reporting to the SVP, Head of Regulatory Affairs, this role will be responsible for the regulatory writing & medical writing deliverables of assigned project(s), in accordance with the agreed timelines and quality standards. As a key member of the cross-functional Development Team responsible for pr

Product marketing, copy writing.

Product marketing, copy writing.

Director, Medical Writing works closely with stakeholders in Clinical Development, Clinical Operations, Biostatistics, and other functional areas and manages medical writing service providers to develop Regulatory documents, including but not limited to clinical study protocols and clinical protocol

Writing/Editing Job Duties: Create content campaigns that align with marketing objectives and company goals Produce, edit and customize content for all our platforms, including our website, LinkedI

The Administrative Assistant will support daily operations by delivering high-quality administrative, clerical, and customer service support.This position helps the office run smoothly, assists the Commercial Lines Manager and Finance Operations Manager, and contributes to a positive client experien

Math Writing Editor Remote Job Duties: The Math Writing Editor ensures that all Eureka Math content—including print and digital curricula, professional development presentations, and public-facing documents—meets our

Professional background in proofreading, editing, journalism, creative or technical writing, or another related field. Technical writing certificate or other related certification (preferred).

Job Opportunity at Ferrari Silicon Valley.GO Auto Group is a globally recognized and award-winning company with an unparalleled dedication to outstanding customer care and operational excellence.GO Auto Group is an industry thought leader representing 27 timelessly modern franchised dealerships in e

BODYROK offers high-intensity, low-impact Pilates workouts that tone, sculpt, and redefine your body and mind in just 45 minutes! We are a rapidly growing company looking for fitness enthusiasts who are: organized, problem-solvers, demonstrate excellent interpersonal skills, and have a passion & exc

Do you want a career and not just a job?.We are a very busy office and are looking for our next great team member.This busy insurance and financial services office has a passion to make a difference in the lives of others and better the community.Our team works hard to reach our goals together as a

Medical Front Desk Receptionist.Rolling Hills Estates, California.At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities.As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden

Receptionist / Front Desk Coordinator.Expected hourly rate range for this job is $25.Applicants must be eligible to work in the United States without visa sponsorship now or in the future*.Rudolph & Sletten, a Tutor Perini Company, is seeking a receptionist / front desk coordinator to join our off

Victory Automotive Group is family owned and operated since 1997 with over 50 locations across the United States.We provide the best opportunities for all employees, customers, communities, and each manufacturer we represent.Our continued commitment is to improve our dealerships and services to sati

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Location: Foster City, CA, 94404, United States.Job Category: Part-time, Off-campus, Department of Industrial Relations.Employee Type: Student Assistant.Agency/Department: Industrial Relations, Dept of.

Strong verbal and written communication skills for report writing, executive summaries, and presenting to leadership teams. Communicates orally, in writing, or through graphic representations and statistical summaries with colleagues, managers, employees, the public, organized employee groups and re

Demonstrates effective interpersonal and communication skills, both verbally and in writing.

Performs high-level administrative and office support responsibilities for assigned leader and leadership team.Coordinates documents and correspondence, including letters, reports, emails, presentations, memos, faxes, etc.Uses appropriate tools for required work including Microsoft Outlook, Word, Ex

Good writing and communication skills.

Legal Administrative Assistant.Gunderson Dettmer has an opening for a Legal Administrative Assistant in our Silicon Valley office.The Legal Administrative Assistant will provide a wide range of hands-on and virtual administrative support to attorneys and paralegals working in our Silicon Valley offi

Administrative Assistant Video Producer.We are seeking a detail-oriented Administrative Assistant Video Producer to join our dynamic Content Suite Team.This role blends administrative excellence with advanced video production.You will utilize cutting-edge generative AI and traditional video editin

Technical writing certificate or other related certification (preferred). Professional background in proofreading, editing, journalism, translating, creative or technical writing, or another related field.

Seeking participants for Focus Group and market research studies.Work part-time from home and earn up to $750 per week.Register to see if you are eligible.Administrative Assistant admin experience not required.Remote Work From Home Administrative Assistant Admin - Part Time Market Research Panelists

Replit is the agentic software creation platform that enables anyone to build applications using natural language.With millions of users worldwide, Replit is democratizing software development by removing traditional barriers to application creation.We are looking for a highly organized and proactiv

If the following job requirements and experience match your skills, please ensure you apply promptly.One Medical is a primary care solution challenging the industry status quo by making quality care more affordable, accessible and enjoyable.But this isn't your average doctor's office.We're on a miss