Quality Engineering Technician

Join Our Mission to Safeguard Humanity!Vaxcyte is at the forefront of clinical-stage vaccine innovation, dedicated to developing high-fidelity vaccines aimed at protecting humanity from the serious and costly implications of bacterial diseases. Our commitment to eradicating or treating infections such as invasive pneumococcal disease, Group A Strep, and Shigella exemplifies our mission. With a clear and well-defined path to success, Vaxcyte is poised to make a significant impact. Our Approach: At Vaxcyte, what we do is as crucial as how we do it. Our collaboration is anchored in four enduring core values: *Rethink Convention: We infuse creativity and diverse thinking into every aspect of our work to continuously innovate how vaccines are delivered. *Aim High: We embrace our bold collective goal to courageously develop the most complex biologics ever attempted to safeguard humanity. *Lead with Heart: Every individual at Vaxcyte leads with a kindness-first, inclusive approach that fosters collaboration and vigorous debate to advance our business objectives. *Model Excellence: The scale of our challenge necessitates a shared commitment to integrity, accountability, equality, and transparency in communication and decision-making.Position Overview:The Associate Director of Quality Control Operations is a pivotal executive role within our global vaccine organization. This position is responsible for implementing Vaxcyte's analytical strategies at our Contract Development and Manufacturing Organizations (CDMOs) and Contract Research Organizations (CROs). Acting as the primary liaison for our CDMOs and CROs, you will ensure the delivery of high-quality, accurate, and compliant testing and analytical services. Collaborating closely with the analytical technical lead and various functions—including Analytics, Process Development, Manufacturing Science, Quality Assurance, and Regulatory Affairs—you will provide leadership and oversight for the execution of analytical strategies supporting analytical readiness and deliverables. You will be accountable for ensuring timely and compliant testing and release at our CDMO and CRO, facilitating a secure and uninterrupted supply of Vaxcyte’s groundbreaking therapies.

Join Our Mission to Safeguard Humanity!At Vaxcyte, we are pioneering vaccine innovations aimed at developing high-fidelity vaccines to combat the dire consequences of bacterial diseases. These diseases pose significant health risks and financial burdens if not addressed. Our commitment extends to eradicating or treating various bacterial infections, including invasive pneumococcal disease, Group A Strep, and Shigella. We have a clear and strategic path to success, positioning Vaxcyte for long-term achievement. Our Approach: We believe that WHAT we do is equally important as HOW we do it! Our collaborative efforts are underpinned by four enduring core values: *RETHINK CONVENTION: We infuse creative and intellectual diversity into every aspect of our work to innovate and continuously improve the delivery of vaccines. *AIM HIGH: Together, we strive toward an ambitious goal of developing the most complex biologics to safeguard humanity. *LEAD WITH HEART: At Vaxcyte, we foster a kindness-first, inclusive approach to leadership, promoting collaboration and open debate that drives our business objectives forward. *MODEL EXCELLENCE: The scale of our challenges calls for a shared commitment to integrity, accountability, equality, and clarity in our communications and decision-making processes.Position Summary:The Senior Director of Global Logistics and Distribution will oversee the shipping and storage of all Vaxcyte CMC materials, including finished goods, bulk products, and samples. This role encompasses materials for Research, Development, Clinical, and Commercial purposes and will report directly to the Executive Director of Global Supply Chain.Key Responsibilities:Strategic Planning:Formulate and execute a global logistics and distribution strategy that aligns with corporate goals, including network design, transportation optimization, and warehousing operations.Operations Management:Guarantee the efficient, timely, compliant, and high-quality delivery of all materials within scope.Ensure robust pack-out designs with appropriate containers and components to maintain materials at target temperatures and facilitate efficient receipt.Establish strong shipping agreements with CMOs and suppliers to ensure seamless operations.

Join Our Mission to Protect Humankind!Vaxcyte is an innovative clinical-stage vaccine company dedicated to engineering high-fidelity vaccines aimed at safeguarding humanity from the devastating impacts of bacterial diseases. Our mission involves not just the eradication but also the treatment of bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella. We have a clear and ambitious roadmap to success, and Vaxcyte is poised to achieve remarkable milestones. What we do is equally important as how we do it! Our collaborative efforts are anchored by four enduring core values: *RETHINK CONVENTION: We foster creative and intellectual diversity in every aspect of our work, continually innovating how vaccines are delivered. *AIM HIGH: We embody our ambitious goal to courageously create the most complex biologics ever developed for the protection of humankind. *LEAD WITH HEART: At Vaxcyte, every individual leads with a kindness-first and inclusive approach to collaboration, encouraging healthy debate that advances our objectives. *MODEL EXCELLENCE: The scale of our challenges necessitates a shared commitment to integrity, accountability, equality, and clarity in communication and decision-making.Position Summary:Vaxcyte offers an exciting opportunity for a Senior Manager, Quality Control Data Analyst to join our Quality Control (QC) organization. This role will serve as a vital link between our technical QC Operations team and Business teams. The successful candidate will be responsible for the systematic collection, evaluation, interpretation, and visualization of complex datasets, transforming them into actionable insights that inform both technical and business decisions. Key responsibilities include generating reports, managing databases, and utilizing analytical tools to identify trends, initiate quality events when necessary, enhance operational efficiency, and support the formulation of acceptance criteria as well as strategic planning.Essential Functions:Collaborate closely with analytical sub-teams and other departments within Analytics, Process Development, Quality Assurance, Operations, and Regulatory functions.Ensure data integrity, accuracy, and reliability, ensuring datasets are evaluated promptly and conform to quality and regulatory standards, thereby securing a continuous supply of Vaxcyte’s innovative therapies.

Role overview The Senior Quality Assurance Specialist at Natera in San Carlos, CA plays a key part in maintaining the quality and reliability of genetic testing products. This position works with teams across the company to shape, apply, and improve quality assurance processes that meet industry standards. What you will do Work with colleagues from different departments to create and update quality assurance protocols Put processes in place and monitor them to support product safety and performance Lead efforts to improve both existing and new products Help ensure compliance with regulatory and industry requirements Impact This role helps make sure Natera’s genetic testing solutions continue to meet high standards for safety and performance.

Join Our Mission to Safeguard Humanity!Vaxcyte is a pioneering clinical-stage vaccine development company dedicated to creating high-fidelity vaccines aimed at safeguarding humanity from the dire consequences of bacterial diseases. Our mission is not just to combat but to eradicate or effectively treat serious bacterial infections including invasive pneumococcal disease, Group A Strep, and Shigella. We have a clear, structured path to success, and Vaxcyte is prepared to lead the charge. Our Approach: Our work is defined by our commitment to four core values: *Challenge the Norm: We infuse creativity and diverse perspectives into all aspects of our endeavors to revolutionize vaccine delivery. *Aim High: We strive to achieve our ambitious goal of developing the most complex biologics ever created to protect humanity. *Lead with Empathy: Every team member at Vaxcyte fosters a collaborative environment that prioritizes kindness and constructive debate, propelling our objectives forward. *Exemplify Excellence: The challenges we face demand a collective commitment to integrity, accountability, and transparent communication.Position Overview:We are on the lookout for a highly motivated and detail-oriented Senior Associate Scientist (Contract) to join our Polysaccharide Analytical Development team. The primary focus of this role is to support the analytical testing and characterization of polysaccharide-based drug candidates. The successful candidate will execute and refine various biochemical and chromatographic assays, contribute to method development initiatives, and ensure the generation of high-quality data in alignment with our research and development programs.This position demands robust hands-on experience with HPLC-based techniques, biochemical assays, and analytical software platforms, alongside a steadfast commitment to data integrity, meticulous documentation, and collaborative efforts across functions.

Role overview Natera is hiring an Associate Director of Biostatistics to join the team in San Carlos, CA. This leadership position oversees a group of biostatisticians and partners with colleagues from multiple departments. The main focus is on designing and analyzing clinical trials that support projects in genomic testing and personalized medicine. What you will do Supervise and mentor a team of biostatisticians Work with cross-functional teams to plan and analyze clinical trials Use statistical programming and analysis methods in healthcare research Contribute statistical data for regulatory submissions Impact This position plays a key role in advancing genomic testing and personalized medicine. The work aims to improve patient care by providing data-driven insights that inform healthcare decisions.

Join Our Mission to Protect Humanity!Vaxcyte is a pioneering clinical-stage vaccine innovation firm dedicated to engineering high-fidelity vaccines designed to safeguard humanity against the dire and costly consequences of bacterial diseases. Our mission extends to eradicating or treating bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella—this is merely the start of our journey. With a clear and well-defined path to success, Vaxcyte is poised to make a significant impact. Our approach is as crucial as the outcomes! Our collaborative efforts are anchored by four fundamental core values: *RETHINK CONVENTION: We infuse creativity and intellectual diversity into every aspect of our work, continuously innovating the delivery of vaccines. *AIM HIGH: We passionately pursue our ambitious goal to develop the most complex biologics ever attempted for the protection of humankind. *LEAD WITH HEART: At Vaxcyte, everyone is a leader, embracing a kindness-first, inclusive approach that fosters collaboration and robust debate to advance our business objectives. *MODEL EXCELLENCE: The magnitude of our challenges necessitates a collective commitment to integrity, accountability, equality, and transparency in our communications and decision-making.Position Overview:The Director of Drug Substance (DS) Commercialization for Critical Raw Materials will spearhead the launch readiness and commercial supply of essential raw materials for the production of engineered Critical Raw Materials (eCRM) and related components for glycoconjugate vaccines. This role encompasses serving as the technical lead and Subject Matter Expert (SME) on biologic raw material processes. The primary focus is on technical launch planning and execution, utilizing best practices while coordinating cross-functional efforts for regulatory submissions, facility readiness, launch supplies, and post-launch process robustness initiatives.This position also involves providing leadership to ensure effective communication regarding the scientific and commercial rationale behind critical raw material manufacturing processes to internal stakeholders, Contract Manufacturing Organizations (CMOs), and regulatory agencies. The incumbent will collaborate with the organization to guarantee timely execution and meticulous planning for commercial lifecycle management.This position reports to the Senior Director of Global DS Commercialization, Protein.

About Obvio AIEvery year, over 7,500 pedestrians lose their lives due to vehicular accidents in the U.S., a staggering increase of 70% over the last decade. Despite heightened awareness, numerous cities find it challenging to combat dangerous driving, resulting in inadequate 'Vision Zero' initiatives nationwide.At Obvio AI, we aim to revolutionize this landscape.We utilize solar-powered, AI-enhanced cameras to enforce traffic regulations in areas where pedestrians are most at risk—automating enforcement in ways that traditional systems and police departments cannot. Our innovative approach has already led to significant reductions in reckless driving and enhanced safety for pedestrians, drivers, and law enforcement.Founded by the creators of Motive’s AI dashcam, Obvio is supported by Bain Capital Ventures and Khosla Ventures. With a recent $22M Series A funding round, we are collaborating with some of the most progressive cities across the nation. Backed by meaningful revenue, a vast market, and strong policy support, we are building the intelligence layer for safer streets on a global scale.About the RoleAs the Head of Annotation Operations, you will oversee our annotation and review function from inception to execution as we expand our capabilities.This position will lead a team poised for substantial growth over the upcoming year. You will be responsible for designing and managing workflows, quality assurance systems, training programs, and performance evaluations essential for operating a high-throughput, safety- and compliance-critical operation.Your ResponsibilitiesAnnotation Operations & Workflow Management:Lead the implementation and ongoing enhancement of Obvio's annotation and review workflows for automated traffic enforcement.Translate enforcement requirements and edge cases into comprehensive review guidelines, task specifications, and escalation pathways.Ensure a balance between throughput, accuracy, and consistency in a high-pressure operational context.Organizational Scaling:Develop the operational framework for a rapidly growing review team, encompassing team structure, leadership roles, and quality assurance functions.Oversee recruitment, onboarding, and training programs to accelerate reviewer proficiency.Establish and manage performance assessment systems, including coaching, feedback, and accountability metrics.

Vaxcyte, based in San Carlos, California, is a clinical-stage vaccine company working to advance vaccines that address serious bacterial diseases such as invasive pneumococcal disease, Group A Strep, and Shigella. The team values creative thinking, ambitious goals, kindness, and integrity as it pursues new solutions in vaccine development. Role overview The Associate Director, Regulatory CMC, plays a key role in both strategy and execution. This position develops and implements global regulatory CMC strategies for investigational products. The role involves leading the preparation and submission of regulatory CMC documents, managing communications with health authorities, and guiding cross-functional teams on regulatory CMC matters. Main responsibilities Develop and execute global regulatory CMC strategies for investigational products. Lead the preparation and submission of regulatory CMC documents. Manage communications with health authorities regarding CMC topics. Provide regulatory CMC guidance to cross-functional project teams. Ensure compliance with global regulatory requirements. Conduct ongoing regulatory surveillance to keep the team informed of changes in regulations.

Join Our Mission to Protect Humankind!Vaxcyte is a pioneering clinical-stage vaccine innovation company dedicated to engineering high-fidelity vaccines designed to safeguard humanity from the severe health impacts of bacterial diseases. Our mission encompasses the eradication and treatment of bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella. With a clear and well-defined path to success, Vaxcyte is committed to making a meaningful difference. Our Approach is as vital as our Results! Our collective work is driven by four core values: *Rethink Convention: We embrace creative and intellectual diversity to innovate and continually improve vaccine delivery. *Aim High: We strive to achieve audacious goals to develop the most complex biologics aimed at protecting humankind. *Lead with Heart: Everyone at Vaxcyte leads with kindness, fostering an inclusive environment that promotes collaboration and healthy debate to meet our business objectives. *Model Excellence: Our challenge demands a shared commitment to integrity, accountability, equality, and clarity in communication and decision-making.Position Summary:Vaxcyte is thrilled to offer an exciting opportunity for a dynamic and skilled individual to join our Analytical Development team. The Associate Scientist II, Analytical Development will be responsible for executing analytical testing and supporting method development activities for our biologics and vaccine development programs. This role will entail performing both routine and non-routine analytical assays utilizing modern analytical techniques and contributing to method optimization, troubleshooting, and continuous improvement initiatives under supervision. Candidates should possess demonstrated hands-on laboratory experience, strong technical execution, and the ability to work independently on routine tasks while supporting more complex development activities.Essential Functions:Analytical Testing & Data GenerationConduct routine and non-routine analytical testing using modern analytical methods (e.g., HPLC/UPLC, SEC, CE, UV-Vis, ELISA, electrophoresis, plate-based assays, and other biochemical or biophysical techniques).Prepare samples, reagents, standards, and controls for testing.

Join Our Mission to Safeguard Humanity!At Vaxcyte, we are a pioneering clinical-stage vaccine innovation company committed to developing high-fidelity vaccines aimed at protecting humanity from the severe health impacts of bacterial diseases. Our mission is to eradicate or effectively treat bacterial infections like invasive pneumococcal disease, Group A Streptococcus, and Shigella, and we have a clear and well-defined path to achieving this goal. Our Approach: What we do is as vital as how we do it! Our collaborative efforts are anchored by four core values: *RETHINK CONVENTION: We embrace creative and intellectual diversity, driving innovation and enhancing vaccine delivery methods. *SET HIGH ASPIRATIONS: We strive to tackle the most complex biologics challenges to protect humankind. *LEAD WITH COMPASSION: Our leadership is rooted in kindness and inclusivity, fostering collaboration and constructive debate to meet our business goals. *MODEL EXCELLENCE: We are dedicated to demonstrating integrity, accountability, and clarity in our communications and decision-making processes.Position Overview:Vaxcyte is on the lookout for an Associate Director of Real-World Evidence & Epidemiology to play a pivotal role in advancing and enhancing our epidemiology and real-world evidence (RWE) capabilities throughout the vaccine lifecycle. Joining our purpose-driven team means contributing to the science of prevention across all stages of life. This role presents a unique opportunity to establish a robust epidemiology and RWE function, offering significant ownership, mentorship, and opportunities for growth.This dynamic, hands-on position is ideal for an early-to-mid-career epidemiologist who thrives on both executing tasks and building functions. The role integrates operational leadership (including study start-up, vendor management, and IRB submissions) with scientific execution, encompassing study design, data analysis, evidence synthesis, and interpretation.As this individual progresses, they will evolve into a scientific epidemiology lead, assuming greater responsibility for study design, analytical strategy, and external scientific collaboration.

Become a Key Player in Our Mission to Safeguard Humanity!Vaxcyte is at the forefront of vaccine innovation, dedicated to creating high-fidelity vaccines to shield humanity from the severe impacts of bacterial diseases. Our efforts are directed towards eradicating or managing bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella. We have a clear and strategically laid-out path to success, and Vaxcyte is geared up to achieve its ambitious goals. Our Approach: At Vaxcyte, the importance of WHAT we do is matched only by our commitment to HOW we do it. Our work is anchored by four core values: *RETHINK CONVENTION: We infuse creativity and intellectual diversity into every aspect of our work to pioneer the future of vaccine delivery. *AIM HIGH: We embrace our audacious goal of developing the most complex biologics to protect humanity. *LEAD WITH HEART: Our inclusive, kindness-first approach fosters collaboration and robust debate that drives our business forward. *MODEL EXCELLENCE: The scale of our challenges demands a collective commitment to integrity, accountability, equality, and clarity in our communications and decisions.Position Overview:The Associate Director of SEC Reporting & Technical Accounting will play a pivotal role in the company’s external reporting and technical accounting functions. Reporting directly to the Senior Director of Technical Accounting & SEC Reporting, this position is highly hands-on, taking ownership of the preparation and execution of SEC filings and technical accounting analyses while managing one direct report.This role is best suited for a technically adept accounting professional who thrives in detail-oriented environments, enjoys cross-functional collaboration, and is eager to help establish processes in a rapidly growing public biotechnology firm.Key Responsibilities:SEC Reporting (Hands-On Execution)Lead the preparation of quarterly and annual SEC filings, including Forms 10-Q, 10-K, and 8-K.Prepare and/or review primary financial statements, footnotes, and related disclosures per U.S. GAAP and SEC requirements.

As a Senior Director of Oncology Clinical Trial Operations at Natera, you will lead and optimize our clinical trial operations in the oncology space, ensuring the successful execution of clinical studies from inception to completion. You'll collaborate with cross-functional teams to develop innovative strategies that align with our mission to improve patient outcomes through precision medicine.Your leadership will be pivotal in managing a team of dedicated professionals, fostering a culture of excellence and continuous improvement. The ideal candidate will possess a deep understanding of oncology clinical trials, regulatory requirements, and an ability to navigate complex project landscapes.

Join Our Mission to Protect Humanity!Vaxcyte is a pioneering clinical-stage vaccine innovation company dedicated to engineering high-fidelity vaccines that aim to safeguard humanity from the severe health implications of bacterial diseases. We are committed to eradicating or effectively treating bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella, with a clear and defined path toward success. Our Approach: What we do is just as vital as how we do it! Our collaborative efforts are anchored by four core values: *RETHINK CONVENTION: We infuse creativity and intellectual diversity into every aspect of our work to innovate and re-innovate vaccine delivery. *AIM HIGH: We embody our ambitious goal to courageously tackle the most complex biologics designed to protect mankind. *LEAD WITH HEART: At Vaxcyte, everyone leads with kindness and inclusiveness, fostering collaboration and spirited debate that drives our business objectives forward. *MODEL EXCELLENCE: The magnitude of our challenge necessitates our collective commitment to integrity, accountability, equality, and clarity in communications and decision-making.Position Overview:The Associate Director of Process Validation and Risk Management will spearhead and facilitate commercial process validation and risk management activities throughout Vaxcyte's comprehensive manufacturing processes. This role is pivotal in shaping technical strategies, executing plans, and coordinating across functions to ensure commercial readiness, regulatory compliance, and effective lifecycle management.The successful candidate will provide leadership to ensure our organization is adept at designing, executing, and communicating process validation and risk management strategies to internal stakeholders, external partners, and regulatory bodies.This position reports to the Senior Director of Process Validation within the Global MSAT organization and collaborates on the overarching validation strategy, with primary accountability for process validation execution and risk management frameworks supporting commercial manufacturing.

Join Our Mission to Safeguard Human Health!Vaxcyte is a pioneering clinical-stage vaccine innovation company dedicated to engineering high-fidelity vaccines aimed at protecting humanity from the dire consequences of bacterial diseases. Our mission to combat and eliminate bacterial infections, including invasive pneumococcal disease, Group A Strep, and Shigella, is just the beginning of our journey. With a clear and well-defined pathway to success, Vaxcyte is poised to make a lasting impact. Our Values are Integral to Our Work: Rethink Convention: We embrace creative and intellectual diversity to continuously innovate how vaccines are delivered.Aim High: We are committed to achieving our audacious goal of developing the most complex biologics to protect humanity.Lead with Heart: We foster a culture of kindness, inclusivity, and constructive debate to advance our business goals.Model Excellence: Our commitment to integrity, accountability, and clarity drives our decision-making and communications.Position Summary:The Director of Quality Assurance – Vendor Management is tasked with executing the global vendor quality strategy, ensuring compliance, scalability, and inspection readiness throughout Vaxcyte’s GxP supplier network. This role will provide leadership and oversight for vendor qualification processes, audits, supplier notifications, and performance management initiatives, ensuring alignment with corporate goals and regulatory standards.As a pivotal quality leader, the Director will engage with cross-functional stakeholders and external partners, promoting continuous improvement, risk-based decisions, and operational excellence within the vendor ecosystem.

Location: San Carlos, CA (on-site) About 1X 1X builds versatile robots in San Carlos, California, with a focus on advancing AI and robotics for everyday life. The team aims to design humanoid robots that work alongside people, learning and adapting as they go. The goal: friendly, useful home robots that fit naturally into daily routines. Role Overview 1X seeks a Director of Maintenance and Repair Operations to build and lead the internal team responsible for keeping robotic systems running smoothly. This leader will shape the full workflow for diagnosing, repairing, and maintaining robots in a hands-on workshop environment. The work will span from early prototype support to scaling up for higher-volume production. The Director will play a key part in improving system reliability, gathering product feedback, and ensuring the company is ready for expanded operations. Success in this role calls for deep technical knowledge, strong operational judgment, and a willingness to work directly with the team in a startup setting. What You Will Do Build and lead the Maintenance and Repair organization for robotic systems. Refine and expand playbooks for diagnosing and troubleshooting complex electromechanical issues at both system and component levels. Create and scale repair workflows, including intake, triage, repair, validation, and return-to-service steps. Hire, coach, and develop a team of repair technicians and diagnostic/service engineers (including both exempt and non-exempt roles). Set clear roles, responsibilities, and career paths within the Maintenance and Repair team. Partner with Quality Assurance to build structured processes for failure tracking, root cause analysis, and ongoing improvement. Work closely with design, manufacturing, and reliability engineering teams to drive product improvements based on real-world and production feedback. Interpret and enforce the use of technical documentation such as schematics, work instructions, and bills of materials (BOMs). Maintain high standards for quality, safety, and traceability throughout operations. Support the shift from low-volume builds to higher-volume production as operations grow.

Join Natera as an Associate/Assistant Laboratory Director specializing in Organ Health. In this pivotal role, you will be responsible for overseeing laboratory operations, ensuring compliance with regulatory standards, and driving innovation in organ health diagnostics. As part of our dynamic team, you will collaborate with experts across various disciplines to enhance our laboratory processes and improve patient outcomes. Your contributions will directly impact our mission to advance genetic testing for organ health.

Join Our Mission to Safeguard Humanity!Vaxcyte is a pioneering clinical-stage vaccine innovation company dedicated to engineering high-fidelity vaccines that shield humanity from the severe and costly health impacts of bacterial diseases. Our mission focuses on eradicating or treating bacterial infections, including invasive pneumococcal disease, Group A Strep, and Shigella, marking just the beginning of our journey. With a clear and well-defined path to success, Vaxcyte is poised to make a lasting impact. Our Approach is as vital as Our Mission! Our collaborative efforts are anchored in four enduring core values: *RETHINK CONVENTION: We infuse creativity and intellectual diversity into every aspect of our work, continuously innovating how vaccines are delivered. *AIM HIGH: We embrace our ambitious goal to courageously tackle the most complex biologics aimed at protecting humanity. *LEAD WITH HEART: At Vaxcyte, everyone plays a leadership role with a kindness-first, inclusive approach that fosters collaboration and constructive debate to advance our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge demands a shared commitment to integrity, accountability, equality, and clarity in communications and decision-making.Position Summary:Vaxcyte offers an exciting opportunity for a proactive and skilled individual to join our Analytical Development team as a Scientist II. In this role, you will execute analytical testing and contribute to the development of analytical methods for biologics and vaccine programs. You will perform both routine and complex analytical assays utilizing cutting-edge techniques, support method optimization and troubleshooting efforts, and engage in continuous improvement initiatives with moderate supervision while collaborating effectively with cross-functional teams. This position requires hands-on laboratory experience, strong technical execution, and problem-solving abilities, along with the capability to independently plan and execute assigned tasks, analyze and interpret data, and initiate or drive investigations as necessary. You will also author and maintain clear technical documentation, including method protocols, development summaries, and SOPs, while communicating experimental results and conclusions to internal stakeholders.

Global Supply Manager, Structures | Supply ChainLocation: San Carlos, CA (on-site)About 1XAt 1X, we are at the forefront of innovation, building humanoid robots that collaborate with humans to address labor shortages and foster a future of abundance.Role OverviewWe are in search of a dedicated Global Supply Manager to lead the global sourcing of structural components such as frames, enclosures, and pivotal structural systems. Your contributions will be crucial in establishing a robust and scalable supply chain that ensures the reliable production of our next-generation humanoid robots.Key ResponsibilitiesFormulate and implement sourcing strategies for structural components, encompassing metals, plastics, and composites.Identify, assess, and onboard global suppliers that fulfill our stringent quality, cost, and delivery criteria.Negotiate contracts, pricing, and delivery terms to secure advantageous agreements.Collaborate with engineering teams to ensure parts meet both mechanical and aesthetic specifications.Support initiatives aimed at cost optimization while maintaining durability and consistency.Conduct supplier benchmarking and stay abreast of technology and pricing trends.Monitor supplier performance metrics to ensure adherence to contractual obligations.Implement risk mitigation strategies, including alternate sourcing and diversification.Provide technical support for Design for Manufacturing (DFM) efforts with an emphasis on structural systems.Manage supplier audits and drive continuous improvements where necessary.Work collaboratively with manufacturing, operations, and quality teams to ensure seamless integration.