Senior Technical Program Manager for Enterprise Software & Clinical Solutions

Join Natera as a Clinical Lab Supervisor, where you'll lead a team of professionals in a dynamic clinical laboratory environment. In this pivotal role, you will oversee daily laboratory operations, ensuring compliance with quality standards and regulatory requirements. Your leadership will foster a culture of excellence and innovation as you mentor and develop staff, driving continuous improvement in laboratory processes.

Join Natera as a Clinical Lab Supervisor, where you will lead and manage laboratory operations while ensuring compliance with standards and regulations. This pivotal role involves supervising laboratory staff, maintaining quality control, and collaborating with cross-functional teams to enhance lab efficiency.

Join Natera as a Lead Clinical Lab Scientist, where you will play a pivotal role in advancing our laboratory operations. We are seeking an experienced and passionate scientist who is ready to lead a team, drive innovation, and ensure the highest quality standards in our clinical laboratory environment.In this role, you will oversee laboratory procedures, mentor junior staff, and collaborate with cross-functional teams to optimize lab performance. Your expertise will be crucial in implementing new technologies and methodologies that enhance our testing capabilities and improve patient outcomes.

Natera, Inc. is hiring a Clinical Lab Scientist I based in San Carlos, CA. This role plays a key part in supporting essential diagnostics by carrying out laboratory tests that directly inform patient care and clinical decisions. What you will do Perform laboratory tests following established protocols Help deliver accurate and timely diagnostic results Uphold quality standards throughout all testing procedures Role impact The work done in this position ensures that patients and clinicians have reliable information for making important healthcare decisions.

Join Natera as a Clinical Lab Scientist II, where you will play a pivotal role in our laboratory operations, contributing to groundbreaking genetic testing technologies. You will be responsible for performing complex laboratory tests, ensuring accuracy and compliance with all regulatory requirements. Your expertise will help us deliver critical insights and improve patient outcomes.

Role Overview The Lead Clinical Laboratory Scientist at Natera, Inc. in San Carlos, CA, plays a key part in specimen analysis and daily lab operations. This position works closely with the supervisor to meet production goals and maintain high standards in laboratory practices. Main Responsibilities Verify specimen accuracy for patient testing and perform required laboratory tests with precision. Support daily laboratory operations by following standard operating procedures and minimizing errors. Maintain Good Laboratory Practices (GLP), reporting any deviations from protocols to management. Complete production tasks on schedule and process all case samples efficiently. Assist the supervisor with projects assigned by management. Serve as the main point of contact on the lab floor when the supervisor is absent. Train new team members in current laboratory procedures and help implement new processes. Support staff competency evaluations alongside the supervisor and laboratory trainer. Deliver specialized training on laboratory instruments and protocols. Troubleshoot and resolve equipment malfunctions and laboratory errors. Understand the full laboratory workflow and address operational issues as they arise. Ensure correct rollout of new laboratory procedures. Communicate laboratory issues and team concerns to supervisors or managers, offering solutions where possible. Report discrepancies in team performance to the supervisor. Provide constructive feedback during team performance evaluations. Participate in regular meetings with the supervisor. Promote professionalism and maintain team morale, serving as a role model for colleagues. Follow all departmental expectations. Handle Protected Health Information (PHI) in both paper and electronic formats, using various technologies as required. Complete all required HIPAA/PHI privacy, policy, and security training within the first 30 days of employment. Stay current with Natera training requirements. Perform other duties as assigned.

Join Natera as a Senior Clinical Scientist in Oncology, where you will play a vital role in advancing our mission to transform the field of oncology through innovative diagnostics. You will leverage your expertise to drive clinical research projects and collaborate with cross-functional teams to support the development of cutting-edge solutions.

Join Our Mission to Safeguard Humanity!Vaxcyte is a pioneering clinical-stage vaccine innovation firm focused on engineering high-fidelity vaccines aimed at protecting humanity from the severe and costly repercussions of bacterial diseases. Our commitment extends to eradicating or treating bacterial infections, including invasive pneumococcal disease, Group A Strep, and Shigella. Our roadmap to success is well-defined, and Vaxcyte is poised for long-term impact. Our Approach: What we do is as crucial as how we do it! Our collaborative efforts are guided by four enduring core values: *RETHINK CONVENTION: We embrace creative and intellectual diversity across all aspects of our work to innovate and transform vaccine delivery. *AIM HIGH: We embody an audacious goal to tackle the most intricate biologics ever conceived to protect humanity. *LEAD WITH HEART: Everyone at Vaxcyte leads with kindness, fostering an inclusive atmosphere conducive to collaboration and vigorous debate that furthers our business aspirations. *MODEL EXCELLENCE: The scale of our challenge demands a collective commitment to integrity, accountability, and clarity in our communications and decision-making processes.Role Summary:We are in search of a dynamic, proactive, and self-motivated Lab Manager to join our expanding Facilities and Lab Operations Team. This role is highly hands-on, overseeing the daily operations of Vaxcyte laboratories, including vendor management, lab supply inventory, equipment maintenance, and new equipment orders. As a pivotal point of contact for lab personnel, the Lab Manager will handle service requests, prioritize and assign tasks, provide training, and nurture a culture of safety and compliance. This role also involves supporting the design of lab space equipment layouts, collaborating with various departments to develop essential SOPs for training, maintenance, calibration, and repair. The Lab Manager will work closely with procurement and lab teams on CAPEX/OPEX budgeting and management of lab assets and service contracts, support installation in lab spaces, and oversee any qualification and validation activities. Additionally, this role will involve providing feedback on lab efficiency, operations, and policies and making recommendations for improvements.

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 Natera as a Lead Biostatistician in Clinical Research, where you will play a pivotal role in the design and analysis of clinical trials. You will collaborate closely with cross-functional teams and contribute to the advancement of innovative healthcare solutions. This is an exciting opportunity to lead statistical programming efforts, ensuring the highest standards of quality and compliance in clinical data analysis.

About 1X 1X, founded in 2015, designs and develops advanced humanoid robots for home use. The company aims to address labor challenges by creating safe, intelligent robots. Every part of each robot, from motor coils to AI, is built in-house, allowing for full control over quality and innovation. The team values technical excellence and recognizes individual contributions. Role Overview: Senior Materials Lab Engineer 1X seeks a Senior Materials Lab Engineer to drive materials innovation for humanoid robotics in San Carlos, California. This role focuses on polymer-based systems, surface science, adhesives, and coatings. The engineer will play a key part in shaping the materials lab and ensuring high standards in both process and results. What You Will Do Independently manage the formulation, processing, surface treatment, bonding, and testing of advanced materials Oversee daily operations and capabilities of the materials lab Establish and maintain lab protocols for rapid prototyping and validation of components Support the transition from raw materials to finished, validated parts used in humanoid robots What We Look For Extensive experience with polymer-based systems, surface science, adhesives, and coatings Strong hands-on skills and attention to detail Ability to work independently and take ownership of lab operations Experience in setting up and running a high-performance materials lab is a plus This position offers the chance to lead impactful projects and contribute directly to the next generation of robotics.

Be a Part of Our Mission to Safeguard Humanity!Vaxcyte is at the forefront of vaccine innovation, focusing on the development of high-fidelity vaccines aimed at protecting society from severe bacterial diseases that can lead to significant health challenges. Our commitment to combating bacterial infections, including invasive pneumococcal disease, Group A Streptococcus, and Shigella, positions us as leaders in the field. With a clear and defined path toward success, Vaxcyte is committed to making a lasting impact on global health. Our Approach: Values that Drive Us We believe that our mission is as important as our methodology. Our work is guided by four foundational values: *RETHINK CONVENTION: We embrace creativity and diverse perspectives to continuously innovate the delivery of vaccines. *AIM HIGH: Our ambitious goal is to develop the most complex biologics designed to protect humanity. *LEAD WITH HEART: Collaboration at Vaxcyte is rooted in kindness and inclusivity, fostering an environment where vigorous debate leads to meaningful outcomes. *MODEL EXCELLENCE: Meeting our challenges requires a collective commitment to integrity, accountability, and clarity in communication and decision-making.Position Summary:The Executive Director of Clinical Regulatory is a leadership role responsible for crafting and executing global regulatory strategies for clinical investigations and the commercialization of vaccines across both adult and pediatric populations. Working closely with Clinical Development and Safety teams, this position will provide regulatory oversight that supports the preparation of clinical development protocols, interpretation and summarization of clinical data, and the creation and management of clinical and pre-clinical regulatory documents. This role also entails liaising with regulatory authorities to secure commercial approval for innovative vaccine products.Candidates should possess extensive experience in developing and executing regulatory strategies for vaccines and preparing investigational and commercial regulatory submissions, such as IND/IMPD, BLA/MAA, and post-approval clinical and safety notifications. Strong communication skills are essential, particularly the ability to simplify complex regulatory issues and effectively convey potential options and opportunities.

Vaxcyte, based in San Carlos, California, develops vaccines aimed at preventing serious bacterial diseases such as invasive pneumococcal disease, Group A Strep, and Shigella. The company’s mission is to advance vaccine science and help protect communities around the world. The team values fresh thinking, high standards, and open communication. Vaxcyte encourages new ideas to improve vaccine delivery, strives for significant progress in biologics, and emphasizes kindness, inclusivity, and clear communication. Integrity and accountability guide their approach to every challenge. Role overview The Senior Manager of Indirect Procurement for Clinical Development leads procurement efforts that support clinical development programs. This role serves as a strategic partner to Clinical Operations and works closely with Finance and Legal. Responsibilities span the entire procurement process for clinical trials, from project initiation through closeout, and require flexibility as indirect spend categories evolve. Key responsibilities Direct procurement support for clinical development initiatives Oversee the requisition to purchase order process for clinical trials Assist with vendor selection and coordinate contracts to ensure engagements are timely, compliant, and cost-effective Work with Clinical Operations, Finance, and Legal teams throughout the procurement lifecycle

Robot Service SupervisorSan Carlos, CA (on-site)About 1XAt 1X, we are pioneering the development of humanoid robots designed to assist humans in addressing labor shortages and fostering abundance in various industries.The RoleAs a Robot Service Supervisor, you will lead and mentor a team of skilled technicians in our service repair shop. Your primary responsibility will be to ensure that the team delivers outstanding service while optimizing operational efficiency. You will work collaboratively with cross-functional teams to tackle challenges impacting service quality, repair efficiency, workstation ergonomics, and equipment upkeep. The ideal candidate will possess strong interpersonal, organizational, and leadership skills, showcasing the ability to instigate innovative solutions and drive positive change.Key ResponsibilitiesLead, mentor, and nurture a high-performing team of technicians to meet service delivery goalsOversee shop records and inventory management to ensure seamless operations within the service centerAct as the process leader for shop activities, refining work standards with input from technicians and diagnostic teamsCollaborate with the Service Manager and key stakeholders to set and achieve objectives related to quality, speed, and cost-effectiveness according to customer and business requirementsPartner with Diagnostic Engineers to spearhead training and development initiatives for techniciansEnsure compliance with safety regulations and the service center's safety protocols among all employeesAssist in schedule management and resolution of technical and personnel challengesConduct regular one-on-one developmental meetings with team members to facilitate professional growth and assess training needs

Join 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 dire consequences of bacterial diseases. Our mission to combat and eradicate bacterial infections—including invasive pneumococcal disease, Group A Strep, and Shigella—is just the beginning. With a clear and defined path to success, Vaxcyte is positioned to make a lasting impact. Our Approach: At Vaxcyte, what we do is as crucial as how we achieve it. Our work is guided by four core values: *RETHINK CONVENTION: We leverage creative and intellectual diversity to innovate and redefine the delivery of vaccines. *AIM HIGH: We pursue our ambitious goal of developing the most complex biologics ever attempted for the protection of humanity. *LEAD WITH HEART: At Vaxcyte, we prioritize kindness and inclusivity in our collaborative efforts, fostering vigorous discussions that align with our business objectives. *MODEL EXCELLENCE: Our shared challenge necessitates a commitment to integrity, accountability, equality, and clarity in all communications and decisions.Summary:Vaxcyte is seeking a dynamic and skilled individual to join our Vaccine Product Development team as a Stability Manager within the Quality Control Unit. This role is vital for managing the stability program for various projects in preclinical and clinical development.In this position, you will play an essential role in implementing and upholding cGMP Stability for all stages of clinical development. Your primary responsibilities will include overseeing stability studies for individual projects and analyzing stability data. You will collaborate closely with QC team members in a highly cooperative and cross-functional environment. The ideal candidate will bring extensive stability experience, ensure compliant operations and documentation, promote open communication, and adopt data-driven methodologies.

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!Vaxcyte is a pioneering clinical-stage vaccine development company dedicated to engineering high-fidelity vaccines aimed at protecting humanity from the severe and expensive health repercussions of bacterial diseases. Our mission extends to eradicating or effectively treating bacterial infections, including invasive pneumococcal disease, Group A Strep, and Shigella. With a clear and strategic path to success, Vaxcyte is poised for significant achievements in this critical field. Our Approach Matters! We are driven by four fundamental core values: *RETHINK CONVENTION: We embrace creativity and intellectual diversity across all aspects of our work to innovate and continuously improve vaccine delivery methods. *AIM HIGH: We are committed to achieving our bold goal of developing the most complex biologics ever created for the protection of humanity. *LEAD WITH HEART: At Vaxcyte, we prioritize a kindness-first, inclusive approach to collaboration and rigorous debate to further our business objectives. *MODEL EXCELLENCE: The challenges we face demand our collective commitment to integrity, accountability, equality, and clarity in communications and decision-making.Position Overview:The Development organization consists of four Process teams: Protein, Polysaccharide, Conjugate Drug Substance (Conjugation), and Drug Product, all supported by Analytical and Formulation Development teams. Vaxcyte is looking for an Associate Engineer II with a solid foundation in vaccine or biologics process development and manufacturing to join our Polysaccharide Clinical Manufacturing/Process Development team.The successful candidate will provide essential technical support for manufacturing activities in collaboration with our CDMO partners, while actively contributing to process development and validation efforts. This role demands a significant laboratory presence (over 50%) and the capacity to independently execute and document experiments, analyze data, and convey results through technical reports and presentations. The ideal candidate will work collaboratively across departments and may also engage with external CDMO partners to facilitate manufacturing campaigns and process transfers.

Join Our Mission to Protect Humankind!At Vaxcyte, we are a pioneering clinical-stage vaccine innovation company dedicated to engineering high-fidelity vaccines aimed at safeguarding humanity from the serious health implications of bacterial diseases. Our efforts focus on eradicating or treating bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella, marking the beginning of our ambitious journey. Our roadmap to success is clear and robust, positioning Vaxcyte for long-term achievements. Our Approach: The significance of WHAT we do is matched only by the importance of HOW we do it! Our collaborative efforts are anchored in four enduring core values: *Rethink Convention: We inject creative and intellectual diversity into every aspect of our work, continuously innovating the delivery of vaccines. *Aim High: We are driven by an audacious collective goal to create the most complex biologics ever developed to protect humankind. *Lead with Heart: Every team member at Vaxcyte leads with a kindness-first, inclusive approach that fosters collaboration and robust debate, propelling us towards our business objectives. *Model Excellence: The magnitude of our challenges demands our shared commitment to integrity, accountability, equality, and clarity in our communications and decision-making processes.We are always on the lookout for bright, dedicated, and innovative individuals who are passionate about making a difference. If you don’t find a suitable role on our Careers Page, we invite you to submit your resume to join our Talent Community for future opportunities. We encourage you to frequently check our Careers Page as we expand our team and add more opportunities.Vaxcyte is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

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.