Senior Scientist, Research and Development

Join Our Mission to Safeguard Humanity!Vaxcyte is at the forefront of vaccine innovation, dedicated to developing high-fidelity vaccines aimed at protecting humanity from serious bacterial diseases. Our commitment to eradicating or effectively treating infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. With a clear and well-defined path ahead, Vaxcyte is positioned for long-term success. Our approach is defined by our core values: *RETHINK CONVENTION: We embrace creative and intellectual diversity to innovate and continuously improve vaccine delivery. *AIM HIGH: We pursue our collective audacious goal of developing the most complex biologics to protect humanity. *LEAD WITH HEART: At Vaxcyte, we lead with kindness and inclusivity, fostering collaborative discussions that propel our business objectives. *MODEL EXCELLENCE: Our significant challenges demand a shared commitment to integrity, accountability, equality, and clear communication.Role Summary:The Senior Manager for Drug Substance (DS) Commercialization will oversee the launch readiness and commercial supply of the conjugate drug substance. This role will facilitate the transition of the conjugate product strategy from the Process Development team to Manufacturing Science and Technology (MSAT) during the late stages of product development. Key responsibilities include technical launch planning and execution, implementing best practices, and coordinating cross-functional efforts for regulatory submissions, facility preparations, and launch materials.The successful candidate will provide leadership to ensure effective communication of the scientific and commercial rationale for the conjugation process to internal stakeholders, relevant Contract Manufacturing Organizations (CMOs), and regulatory bodies. Exceptional written communication skills are essential, particularly in authoring submissions to Health Authorities (IND/BLA). The ability to collaborate with individuals from diverse backgrounds and perspectives is crucial for success in this role.

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.

Join Our Mission to Protect Humanity!Vaxcyte is a pioneering clinical-stage vaccine development company dedicated to engineering high-fidelity vaccines aimed at safeguarding humanity from the dire impacts of bacterial diseases. Our goal is to eradicate or effectively manage bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella. With a clear and well-defined path to success, Vaxcyte is positioned to achieve remarkable advancements in public health. Our Approach: What we do is just as important as how we do it! Our collaborative efforts are driven by four enduring core values: *RETHINK CONVENTION: We embrace creative and intellectual diversity in our work, innovating and re-innovating the delivery of vaccines. *AIM HIGH: We embody our audacious goal of courageously developing the most complex biologics ever created to protect humanity. *LEAD WITH HEART: Every team member at Vaxcyte leads with a kindness-first, inclusive approach, fostering collaboration and robust discussion that propels our business forward. *MODEL EXCELLENCE: The scale of our challenge necessitates a shared commitment to integrity, accountability, equality, and clarity in communication and decision-making.Position Summary:Vaxcyte is currently seeking a Senior Associate Scientist (Contract) specializing in Conjugation Development. This role will support the development of a robust process for generating our proprietary pneumococcal conjugate vaccine. Responsibilities include reviewing analytical data and electronic notebook entries for accuracy and compliance with standard operating procedures (SOPs). This is a remote, part-time position offering flexible working hours, requiring exceptional organizational skills, clear communication, and meticulous attention to detail.

Be Part of Our Mission to Safeguard Humanity!Vaxcyte is a pioneering clinical-stage vaccine innovation company dedicated to engineering high-fidelity vaccines aimed at protecting humanity from the severe and costly repercussions of bacterial diseases. Our mission goes beyond just addressing invasive pneumococcal disease, Group A Strep, and Shigella; we are committed to eradicating or treating bacterial infections through innovative solutions. With a clear and defined pathway to success, Vaxcyte is poised to make a significant impact in the field of vaccines. Our Work Ethos: What we achieve is equally matched by how we achieve it. Our collaborative efforts are underpinned by four enduring core values: *Rethink Convention: We embrace creative and intellectual diversity to innovate and continuously enhance vaccine delivery methods. *Aim High: We collectively strive to accomplish our ambitious goal of developing the most complex biologics to protect humankind. *Lead with Heart: At Vaxcyte, every individual leads with a kindness-first approach, fostering inclusive collaboration and constructive debate that propels our business objectives forward. *Model Excellence: Given the magnitude of our challenges, we commit to demonstrating integrity, accountability, equality, and clarity in our communications and decision-making processes.Position Summary:We are currently seeking a Scientist II in Conjugation Development. The selected candidate will primarily lead and execute experimental activities supporting our pneumococcal conjugate vaccine program, focusing on enhancing the understanding of the conjugation process. Concurrently, this role involves developing the conjugation process for Vaxcyte’s pipeline programs, contributing to process optimization, scalability, and readiness for future clinical manufacturing. Key responsibilities include the preparation, purification, and analytical characterization of chemically modified polysaccharides and polysaccharide-protein conjugates. The ideal candidate will have substantial laboratory experience and a robust understanding of analytical chemistry principles, with the ability to design, execute, and troubleshoot experiments independently. Additionally, contributions to analytical development and stability studies may be required. Responsibilities will also encompass record management and data presentation to the team.

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 Safeguard Humanity!Vaxcyte is at the forefront of vaccine innovation, developing high-fidelity vaccines aimed at protecting humanity from the dire consequences of bacterial diseases. Our commitment to eradicating or treating infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. With a clear and actionable pathway to success, Vaxcyte is perfectly positioned to make a lasting impact. Our Approach is as crucial as Our Goals! We are guided by four enduring core values: *RETHINK CONVENTION: We foster creative and intellectual diversity in every aspect of our work to continuously innovate the delivery of vaccines. *AIM HIGH: Our audacious collective goal drives us to tackle the most complex biologics ever created for the benefit of humankind. *LEAD WITH HEART: At Vaxcyte, we prioritize kindness and inclusivity in our collaborations and vigorous discussions that propel our business objectives forward. *MODEL EXCELLENCE: The magnitude of our challenge demands a shared commitment to integrity, accountability, equality, and transparency in our communications and decision-making processes. Position Overview:We are seeking a dynamic and skilled individual to join our Drug Product Development team. The ideal candidate will possess a solid understanding and hands-on experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) utilizing various methods, particularly immunoassays and multiplexed formats. Experience with vaccine and adjuvant-containing formulations is a significant advantage.Additionally, we value flexibility and the ability to manage multiple projects simultaneously while adeptly prioritizing tasks to meet aggressive deadlines. This laboratory-based role demands excellent scientific judgment, independence, rigor, and meticulous record-keeping.Key Responsibilities:Perform both routine and non-routine analyses of internal release, development, and stability samples utilizing a diverse range of analytical techniques, ensuring the production of high-quality data and comprehensive reporting.

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.

About 1XAt 1X, we are a pioneering AI and robotics company headquartered in Palo Alto, California. Our mission is to create a society of abundance through innovative general-purpose robots that are capable of performing a wide range of tasks autonomously.We believe that for humanoid robots to genuinely understand the world and enhance their intelligence, they must learn and live alongside humans. This belief drives us to develop friendly home robots that seamlessly integrate into everyday life.Role OverviewWe are seeking an astute, commercially savvy Senior Commercial Counsel to join our expanding Legal team. In this pivotal role, you will serve as the primary legal advisor for all commercial legal matters, managing our entire contract lifecycle, advising on deal structures, and collaborating closely with Supply Chain, Partnerships, Product, and Finance teams to facilitate business growth while minimizing friction. This position offers significant impact and autonomy, making you a vital business partner and advisor.

Global Supply Manager, Motors & Magnets | Supply ChainLocation: San Carlos, CA (on-site)About 1XAt 1X, we are at the forefront of innovation, creating humanoid robots designed to collaborate with humans in tackling labor shortages and fostering abundance in various industries.Position OverviewWe are on the lookout for a skilled Global Supply Manager who will spearhead the sourcing and supply chain strategies for motors, gearboxes, and magnetic assemblies essential for the high-performance and scalable production of our advanced humanoid robots.Key ResponsibilitiesFormulate and implement effective sourcing strategies for motors, gearboxes, magnets, and associated components.Identify, assess, and onboard international suppliers that align with our quality, cost, and delivery benchmarks.Negotiate terms of contracts, pricing, and delivery schedules to ensure advantageous agreements.Collaborate with engineering teams to confirm that components meet performance and quality standards.Drive initiatives for cost optimization while maintaining high reliability and performance.Conduct thorough supplier benchmarking and stay updated on technological advancements and pricing trends.Track supplier performance metrics, ensuring compliance with contractual obligations.Develop risk mitigation strategies, including alternative sourcing and diversification plans.Provide technical assistance for Design for Manufacturability (DFM) initiatives focusing on electromechanical systems.Oversee supplier audits and implement necessary improvements.Work closely with manufacturing, operations, and quality assurance teams to ensure seamless integration.

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.

Role overview Natera seeks a Senior Manager of Research and Development to join the Oncology Product Development team in San Carlos, CA. This leader will oversee the development and optimization of next-generation sequencing (NGS)-based oncology diagnostic assays. The role also includes supporting product lifecycle management after launch. Success depends on technical leadership, strong collaboration across teams, and attention to product performance and scalability. What you will do Direct the technical development of NGS-based oncology assays, including project planning, execution, and coordination with multiple teams. Lead assay development from feasibility through verification and validation within a regulated CLIA environment. Work in partnership with Research, Informatics, Statistics, Software, Regulatory, Quality, and Commercial teams to bring products from concept to launch. Support post-launch activities such as process improvements, troubleshooting, and collaboration with Operations on commercialized assays. Prepare and review technical documents, including study protocols, reports, and validation materials to meet regulatory and product requirements. Mentor and manage team members, fostering their professional growth. Lead and oversee data analysis using statistical methods. Requirements PhD in Molecular Biology or a related field with at least 6 years of relevant industry experience, or BS/MS with a minimum of 8 years in biotech, including at least 2 years in management. Hands-on experience developing NGS-based assays in a regulated setting; CLIA experience preferred. Familiarity with CLIA laboratory workflows and implementing assays in production. Track record of leading projects and collaborating across functions; people management experience is a plus. Experience with high-throughput workflows or automation is beneficial. Knowledge and skills Strong technical background in oncology diagnostics and NGS technologies. Analytical thinking and problem-solving abilities. Proficiency in technical writing and documentation for regulated environments. Understanding of regulatory standards and design control processes, including LDT, CAP/CLIA, product development lifecycle, and change management. Excellent collaboration, communication, and interpersonal skills.

Role Overview Vaxcyte is hiring a Senior Manager, Supply Chain Planning in San Carlos, California. This leader will guide a team responsible for demand planning, inventory management, and supplier coordination. The work supports smooth production and distribution of Vaxcyte’s vaccine products.

Role overview Natera Inc. seeks a Senior Product Manager specializing in Oracle Fusion Supply Chain Management (SCM) at its San Carlos, CA office. This position shapes the direction of SCM products and serves as a bridge between product development, customer needs, and evolving market trends in healthcare technology. Collaboration with teams across the company is central to this role. What you will do Define and manage the strategy and roadmap for Oracle Fusion SCM solutions Collaborate with engineering, operations, and cross-functional groups to deliver new features and ongoing improvements Spot opportunities to enhance SCM offerings by monitoring market trends and gathering customer feedback Align product development efforts with Natera’s objectives and the requirements of healthcare clients About Natera Natera creates technology-driven solutions for the healthcare industry, emphasizing innovation and meaningful results for customers.

Position Summary The Senior Marketing Manager for NIPT will be responsible for crafting and implementing innovative marketing strategies aimed at enhancing the adoption of Natera’s genetic testing solutions, user experience offerings, and educational tools for patients. This is an exceptional opportunity to be part of a dynamic marketing team, developing multi-channel campaigns that make a significant impact on healthcare for countless patients. This position reports directly to the Director of NIPT and Hereditary Cancer Marketing. Primary Responsibilities Market Awareness and Adoption: Create and execute comprehensive marketing plans that amplify awareness and promote critical Panorama NIPT and Vistara Single-Gene NIPT messaging through effective marketing and sales channels. Develop and implement healthcare provider (HCP) and patient marketing campaigns, content, and engagement strategies to effectively communicate the value and foster the adoption of Panorama, Vistara, and related support services. Present marketing campaigns, their progress, and performance metrics to internal stakeholders to ensure alignment with overarching business objectives and facilitate campaign optimization. Cross-Functional Collaboration: Work closely with various departments to align marketing strategies and initiatives with business goals, ensuring seamless integration of marketing efforts across the organization.

Aetherflux develops advanced satellites to reshape the orbital economy, focusing on solar energy capture, energy transmission using infrared lasers, and high-bandwidth optical data delivery. The company, founded in 2024 by Baiju Bhatt (Robinhood co-founder), draws on expertise from leading aerospace and defense backgrounds and is backed by prominent investors. Aetherflux aims to transform how energy and data move in space and on Earth, taking on complex technical challenges to build new space infrastructure. Role overview The Senior Sourcing and Procurement Manager will drive hardware sourcing for Aetherflux’s ambitious satellite programs. This individual contributor role manages the full lifecycle of purchase orders and supplier relationships, ensuring teams receive the materials, components, and services needed to meet rapid development goals. The position suits someone who thrives in a high-growth environment and combines analytical rigor with practical supply chain execution. Advancement to supervisory or managerial roles is possible as the company grows. What you will do Oversee purchase orders from initiation through completion, including supplier negotiations, risk mitigation, and vendor management for key projects. Develop and maintain sourcing tools and dashboards to track supplier performance, spending, and delivery accuracy. Lead cost-saving efforts by working with suppliers and identifying opportunities for manufacturing or process improvements. Manage procurement workflows, conducting pre-award reviews to ensure quality and compliance in purchasing packages. Identify and implement automation to streamline procurement and reduce manual work. Work closely with engineering, finance, and operations teams to support hardware development and production. Requirements This role requires experience managing sourcing and procurement for engineered products, strong analytical and negotiation skills, and a hands-on approach to supply chain operations. Comfort working in a fast-moving, high-growth setting is essential.

Join 1X as a Senior Sourcing Manager - Indirect OperationsLocation: San Carlos, CA (on-site)About 1XAt 1X, we are pioneering the development of humanoid robots that collaborate with humans to address labor shortages and foster a culture of abundance in the workforce.Role OverviewWe are looking for a dynamic Indirect Team Manager to spearhead our Infrastructure and Indirect Sourcing initiatives. This role will be pivotal in cultivating and scaling a highly effective sourcing team that will support facilities, IT infrastructure, factory operations, and corporate services as we expand. Your expertise in judgment, prioritization, and people leadership will be essential in navigating our evolving environment.Your ResponsibilitiesLead and mentor a team of Global Sourcing Managers and Sourcing Specialists.Develop and implement the indirect sourcing strategy across our global locations.Collaborate closely with Facilities, IT, Manufacturing, Real Estate, Finance, and HR to align goals.Establish priorities, manage escalations, and synchronize sourcing efforts with company growth objectives.Drive initiatives for cost optimization, supplier performance enhancement, and risk management.Formulate sourcing strategies and operating models for infrastructure and indirect expenditures.Assist in planning infrastructure for new locations, expansions, and operational scalability.Team-Based Commodity OversightIT infrastructure and network servicesFacilities maintenance and site servicesConstruction, CapEx, and site expansionFactory production support (tooling, MRO, consumables)Corporate services (travel, HR-related services)Commodity management will be distributed among team members based on their experience and business requirements.

Join Our Team as a Senior Identity & Access Management (IAM) Lead in Security & ITLocated in San Carlos, CA (on-site)About 1XAt 1X, we are pioneering the creation of humanoid robots that collaborate with humans to address labor shortages and foster abundance across various industries. Our innovative approach is reshaping the future of work.Your RoleAs the Senior IAM Lead, you will take charge of developing and scaling our identity ecosystem, ensuring that access management is secure, automated, and compliant with audit requirements, all while maintaining high operational efficiency for our teams. This hands-on leadership position involves designing, implementing, and managing our IAM infrastructure across critical systems. You will focus on creating automation-driven lifecycle processes, enhancing authentication measures, and establishing robust governance standards. Your contributions will be vital in supporting our secure growth as we broaden our workforce and technological capabilities.Key ResponsibilitiesOversee end-to-end IAM operations utilizing tools such as Okta, Google Workspace, 1Password, and HRIS for lifecycle management.Develop and automate workflows for onboarding, transitioning, and offboarding personnel to facilitate swift and secure processes.Standardize single sign-on (SSO) and SCIM integrations across SaaS applications with a focus on secure practices.Design and implement role-based access control (RBAC), governance frameworks, administrative boundaries, and approval workflows.Enhance authentication and access controls through risk-based policies, least privilege principles, and privileged access management protocols.Directly configure, troubleshoot, and refine IAM systems, minimizing reliance on external consultants.Create dashboards, metrics, and streamlined documentation to monitor identity health as we expand.Ensure comprehensive revocation of access and credentials during offboarding processes.Maintain organized and well-governed 1Password vaults with clear ownership and regular credential rotation.

Join Our Mission to Safeguard Humanity!At Vaxcyte, we are pioneering innovative vaccine solutions designed to protect humanity from the severe and costly impacts of bacterial diseases. Our commitment extends to addressing critical infections such as invasive pneumococcal disease, Group A Strep, and Shigella. With a clear and defined pathway ahead, Vaxcyte is poised for success in the fight against bacterial infections. Our Approach: We Value Both What We Do and How We Do It! Our collaborative efforts are driven by four core values: *RETHINK CONVENTION: We inject creativity and diverse intellect into every aspect of our work, continually innovating the vaccine delivery process. *AIM HIGH: We embrace ambitious goals, boldly tackling the complexities of biologics to safeguard human health. *LEAD WITH HEART: Vaxcyte fosters a culture of kindness and inclusivity, encouraging robust discussions that propel our objectives. *MODEL EXCELLENCE: Our challenges require a unified commitment to integrity, accountability, and clear communication.Position Overview:The Director of Device Development and Commercialization will oversee the VAX-31 drug product, an intricate biological entity consisting of 31 Drug Substances formulated as an adjuvanted suspension Drug Product. The role demands meticulous attention to the development of a pre-filled syringe (PFS) combination product for both clinical and commercial applications. We seek an enthusiastic and skilled professional to lead our Drug Product Development Team through essential development and regulatory milestones, ensuring our product's successful launch and distribution.The VAX-31DP presents unique challenges in production, handling, and testing due to its suspension system. The director will navigate these complexities by managing their team and collaborating within a matrix structure across the broader Drug Product and commercial organization. Furthermore, it is essential to comprehend, manage, and effectively communicate these challenges to regulatory bodies through compelling submissions. Experience in the vaccine sector, particularly with adjuvants, is highly desirable.

Join our dynamic team at Artech Information Systems LLC as a Senior Research Associate. In this role, you will be responsible for conducting in-depth research, analyzing data trends, and presenting findings to drive strategic decision-making. You will collaborate with cross-functional teams to support ongoing projects and contribute to innovative solutions within the organization.