Manager of Document Management in Analytical Development & Quality Control

Revolution Medicines develops targeted therapies for patients with RAS-addicted cancers. The company’s pipeline includes RAS(ON) inhibitors such as daraxonrasib (RMC-6236), elironrasib (RMC-6291), zoldonrasib (RMC-9805), and RMC-5127, each focused on specific oncogenic variants of RAS proteins. The team is dedicated to advancing treatments for those affected…

Join Revolution Medicines, Inc. as a Senior Manager of Analytical Development and Quality Control, where you will lead innovative projects aimed at enhancing our drug development processes. You will oversee the analytical development strategy, ensuring compliance with regulatory standards and advancing our mission to bring transformative therapies to patients in need.

Revolution Medicines develops targeted therapies for patients with RAS-addicted cancers. The company’s clinical pipeline includes RAS(ON) inhibitors aimed at specific oncogenic RAS protein variants, such as daraxonrasib (RMC-6236), elironrasib (RMC-6291), zoldonrasib (RMC-9805), and RMC-5127. The team is committed to advancing treatments for cancers driven by RAS pathway mutations. The Director of Stability Management, Analytical Development & Quality Control will lead outsourced stability studies for drug substances and products, spanning early clinical through commercial phases. This Redwood City-based position sets the direction for stability programs, ensures compliance with ICH and cGMP standards, and supports global regulatory submissions. Collaboration with internal teams and external partners is central to achieving clinical and commercial objectives. What you will do Set and execute the strategic direction for stability programs, aligning with ICH guidelines and regulatory standards. Supervise the design, execution, and management of stability studies for development, registration, and commercial phases. Collaborate closely with CMC, quality, regulatory, and clinical teams to achieve stability goals. Analyze stability data, perform trend and statistical analyses, and prepare reports to support retest and shelf-life extensions as well as storage recommendations. Work with quality teams during stability-related quality events or investigations and help implement CAPAs at contract organizations. Act as the primary contact for contract organizations on all stability-related activities. Oversee sample shipments, inventory tracking, and chain of custody for stability studies when required. Contribute to drafting CMC stability documentation for IND, NDA, AR, and IMPD submissions across all clinical and commercial phases. Requirements Extensive experience managing stability studies across commercial, late, and early clinical development stages. In-depth understanding of ICH and cGMP guidelines. Proven ability to collaborate effectively within cross-functional teams and with external partners. Experience contributing to global regulatory filings related to stability. Strong organizational and analytical skills.

With over 25 years of dedication to the science of cortisol, a vital hormone linked to numerous diseases, Corcept Therapeutics is making significant strides in the healthcare sector.Our innovative commercial portfolio includes advanced treatments for hypercortisolism and oncology, and we've pioneered over 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. Through ongoing clinical trials for conditions such as hypercortisolism, solid tumors, ALS, and liver disease, Corcept is harnessing the therapeutic potential of cortisol modulation to tackle some of the most challenging health issues faced by patients today.Headquartered in Redwood City, California, we invite you to learn more about our mission at www.corcept.com.We are looking for an Associate Director to spearhead our Document Control Program, a critical component of our Quality Management System (QMS). This leadership position calls for a proven expert in document control, capable of identifying and addressing key gaps while establishing sustainable, risk-based controls that comply with GxP standards. The role encompasses strategy development, program execution, and adherence to compliance requirements, including management of supporting software.As a pivotal leader, you will foster a culture of engagement and accountability regarding Standard Operating Procedures (SOPs) across departments, ensuring that all stakeholders adhere to Corcept’s SOP standards. This includes overseeing and coordinating SOP updates from minor adjustments to extensive system renovations under tight deadlines.The ideal candidate will be a resilient and focused leader who effectively delivers high-impact changes, drives implementation with clarity, and adeptly manages shifting priorities. You will communicate a clear and inspiring vision while guiding teams through transitions with a collaborative leadership style.Experience in pharmaceutical or biotechnology settings is essential, particularly with multi-product transformations that include designing scalable business processes, modifying computer systems, and updating metadata.This is a hybrid role that typically requires an on-site presence at least three days a week.

Revolution Medicines, Inc. is seeking a dynamic and strategic Vice President of Analytical Development & Quality Control to lead our efforts in delivering innovative solutions in the field of biopharmaceuticals. This leadership role will be pivotal in establishing and overseeing cutting-edge analytical methodologies and quality control processes to ensure the safety and efficacy of our drug candidates. The ideal candidate will possess a deep understanding of analytical development within a pharmaceutical context, coupled with a proven track record of leading teams in successful drug development programs. You will be responsible for developing and implementing strategies that align with our corporate objectives while ensuring compliance with regulatory requirements.

Role Overview Adverum Biotechnologies, Inc. is hiring a Quality Control Manager for the Contract Testing Lab (CTL) in Redwood City, CA. This role leads quality assurance efforts to ensure products consistently meet established standards. What You Will Do Oversee daily quality control operations in the Contract Testing Lab Guide and support a team focused on compliance with regulatory requirements Implement and maintain quality control procedures to uphold product standards About Adverum Adverum Biotechnologies develops therapies aimed at improving patient outcomes. The Quality Control Manager plays a key part in supporting this mission by ensuring rigorous standards in laboratory practices.

Join our dynamic team at Mindlance as a Quality Control Specialist, where you will play a crucial role in ensuring our products meet the highest quality standards. You will be responsible for conducting thorough inspections and testing of products, developing quality assurance processes, and collaborating with cross-functional teams to drive continuous improvement.

At Dexterity, we envision a world where robots enhance the human experience. Our innovative technology empowers individuals to focus on creative, inspiring, and problem-solving tasks, while robots efficiently manage repetitive and physically demanding work.We are pioneering warehouse automation, addressing the urgent demand for smarter and more resilient supply chains that affect millions globally. Dexterity's comprehensive robotics systems are designed to pick, move, pack, and collaborate with human-like precision, awareness, and learning capabilities. Our software-driven, hardware-agnostic systems have successfully picked over 15 million items in production. Our unwavering focus on customer needs drives every decision, as we strive to empower our clients with robotic solutions that exceed their expectations.As one of the fastest-growing companies in the robotics field, Dexterity is backed by distinguished investors such as Kleiner Perkins, Lightspeed Venture Partners, and Obvious Ventures. We pride ourselves on our diverse, multidisciplinary team, fostering a culture rich in passion, trust, and commitment. Join us at Dexterity and play a pivotal role in bringing intelligent robots to life!We are in search of a proactive and skilled individual to assume the role of Manufacturing Engineer - Document Control. In this capacity, you will oversee all facets of Engineering Change Order (ECO) and Bill of Material (BOM) management, ensuring these vital documents are accurate, current, and comprehensive. Your responsibilities will include creating, revising, and maintaining BOMs, coordinating configuration management processes, and managing BOM modifications through stringent change control protocols. Collaborating closely with Engineering, Manufacturing, and Supply Chain teams, you will confirm component availability and specifications while identifying cost-saving initiatives and process enhancements.This position demands a blend of technical acumen, project management expertise, and cross-functional collaboration skills, essential for ensuring the precision and efficiency of our product information management systems while successfully transitioning products to volume manufacturing to meet market demands.

Join Poshmark Inc. as a Senior Manager of Operations Analytics, where you will play a pivotal role in driving data-driven decisions that influence our operational strategy. You will lead analytical projects, providing insights to optimize our processes and enhance overall performance.

Retro seeks a Lead Analytical and Product Quality Specialist to support small molecule development in Redwood City, CA. This role manages analytical methods, oversees product quality, and leads ongoing process improvements within the team. Role overview This position focuses on analytical testing and method development for small molecule products. The specialist ensures that product quality standards are maintained from early development through production, taking a hands-on approach to quality systems and workflow enhancements. Key responsibilities Oversee analytical testing and develop methods for small molecule product lines Monitor and uphold product quality standards throughout all stages of development and manufacturing Lead projects aimed at improving quality systems and operational workflows Collaborate with cross-functional teams to advance new product development Maintain compliance with applicable regulatory requirements Requirements Background in analytical chemistry, quality assurance, and regulatory compliance Experience supporting product development in a small molecule environment Strong attention to detail and the ability to work collaboratively across teams

Join Revolution Medicines as a Senior Scientist I in Analytical Development, where you will play a pivotal role in advancing our innovative therapeutics. This position offers an exciting opportunity to contribute to the development of cutting-edge analytical methods and techniques that are crucial for our drug development pipeline. You will collaborate with cross-functional teams to ensure the successful delivery of high-quality data and analytical support.

At DevDocs, we seek talented developers dedicated to crafting exceptional documentation and innovative tools for our esteemed clients, including Qualcomm, American Express, and C3 AI.We pride ourselves on our technical expertise, ensuring our team is composed of individuals who not only understand our clients' products but can also offer consultancy, design automated documentation processes, and create vital documentation themselves.This position is a full-time, in-person role located at C3 AI’s office in Redwood City, California, where you will collaborate closely with fellow DevDocs engineers on documentation projects for C3 AI.Your ResponsibilitiesAs a pivotal player in a leading enterprise AI organization, you will engage with a range of products, including those focused on equipment reliability, generative AI, and demand forecasting.You will work directly with specific engineering teams to gain deep domain knowledge while partnering with the broader DevDocs team on significant initiatives.This role blends engineering, teaching, and tool-making, where you will:Quickly familiarize yourself with new technologies at C3 AI and simplify complex concepts.Create tools and AI workflows for streamlined project execution.Craft essential documentation and devise methods for systematization.Resolve complex knowledge architectures and improve upon existing code structures.Engage in detailed inquiry to uncover root issues and simplify processes.Enhance DevDocs through innovative processes, tools, and experimentation.

SB Energy develops, owns, and operates large-scale energy and data center infrastructure projects across the United States. Backed by SoftBank and Ares, the company has expanded since 2019 to manage over 3 gigawatts in operation, with a robust pipeline of additional projects nationwide. SB Energy uses advanced technology, including an AI-driven digital platform, to deliver reliable and affordable energy for growing demand. With headquarters in Redwood City, CA, and offices in Denver, CO and San Diego, CA, SB Energy focuses on accelerating the shift to cleaner, more sustainable energy sources. The company emphasizes innovation, teamwork, and strong execution to shape the future of energy and technology. Role overview The Senior Manager, Data Center Controls Engineering, leads the design, standardization, and deployment of control systems for data center projects. This position ensures that Building Management Systems (BMS), Electrical Power Monitoring Systems (EPMS), and related controls infrastructure are scalable, reliable, and fully integrated to support high-performance, mission-critical operations. Beyond technical oversight, this role manages and develops a team of controls engineers. The Senior Manager is responsible for maintaining consistency, quality, and ongoing improvement across a growing portfolio of data center campuses. Location Redwood City, CA; Denver, CO; San Diego, CA; or remote.

Join Zum as the Head of SOX and Internal Controls!At Zum, we are on a mission to revolutionize school transportation. As a dynamic Series E startup, supported by prominent investors like Sequoia Capital, SoftBank, Spark Capital, and GIC, we are expanding our innovative services across the U.S. With operations in over 15 states and plans for further growth into the East Coast and Midwest, we are not just a transportation service; we are a technology-driven company harnessing cutting-edge solutions to enhance school district transportation systems. Our initiatives include launching a proprietary charter platform, developing SaaS offerings, and electrifying school transportation fleets to support local utilities. Recognized as a CNBC 50 Disruptor and featured in the Financial Times as one of the 500 fastest growing companies, we invite you to be part of our journey!What You'll Be Doing:In this pivotal role, you will lead the implementation of internal controls and the periodic testing of internal controls over financial reporting (ICFOR). Collaborating closely with our outsourced service provider, you will ensure effective SOX compliance, overseeing the entire SOX compliance program while reporting directly to the VP Corporate Controller.Your Key Responsibilities:Financial Risk Management:• Conduct comprehensive risk assessments across pivotal financial processes to identify control gaps and emerging risks.• Develop and implement a robust internal controls framework aligned with the COSO model, ensuring data integrity and reporting accuracy.• Manage the day-to-day execution of the controls program by coordinating with co-sourced partners, ensuring alignment with internal standards and timelines.Continuous Process Improvement:• Monitor and enhance existing processes to ensure ongoing compliance and operational excellence.

Join Box: The Leader in Intelligent Content Management Box is at the forefront of Intelligent Content Management, serving over 115,000 organizations globally, including nearly 70% of the Fortune 500. We empower leaders in regulated industries to secure their data, enhance collaboration, and streamline workflows using our innovative enterprise AI solutions. At Box, you will play a pivotal role in advancing our platform. Content is the heartbeat of our operations, driving the flow of billions of files and essential information daily—ranging from contracts and invoices to employee records and marketing assets. Our mission is to inject intelligence into content management, enabling our customers to revolutionize their organizational workflows. With the integration of AI and content management, the potential for transformation has never been more significant, and you will be at the forefront of this change. Founded in 2005 and headquartered in Redwood City, CA, Box also has a strong presence across the United States, Europe, and Asia.

Corcept Therapeutics has spent more than 25 years advancing research into cortisol, a hormone linked to many diseases when not properly regulated. The company’s commercial portfolio features therapies for hypercortisolism and oncology, built on a foundation of over 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. Corcept continues to run advanced clinical trials in areas such as hypercortisolism, solid tumors, ALS, and liver disease. Corcept Oncology seeks an Associate Director, Digital & Commercial Analytics, based in Redwood City, California. This position focuses on leading next best action (NBA) orchestration and advanced analytics within the marketing and market access teams. The role involves co-designing, deploying, and maintaining NBA orchestration, as well as delivering analytics that inform marketing performance, digital engagement, and market access strategies. What you will do Co-lead the design and rollout of NBA orchestration across digital and commercial channels Monitor and refine NBA processes to ensure effectiveness and alignment with business goals Deliver analytics to support marketing performance, digital engagement, and market access initiatives Work closely with Digital Marketing, Commercial Operations, Market Access, IT, and external partners Requirements Strong experience in data-driven decision-making and orchestration platforms such as Salesforce Marketing Cloud or CRM systems Background working in complex, matrixed commercial organizations Expertise in decision sciences, personalization, and digital analytics Pharmaceutical industry experience is preferred but not required; candidates from other sectors with relevant skills are encouraged to apply Learn more about Corcept Therapeutics at www.corcept.com.

ControllerLocation: Redwood City, CAAbout QuiltAt Quilt, our mission is to transition humanity away from fossil fuel heating, as homes contribute to 20% of US global warming emissions—surpassing cars. Founded by industry veterans from Google, Apple, Nest, and Tesla, we are at the forefront of developing advanced energy systems that enhance the health and comfort of buildings. We are pioneering the first major HVAC manufacturer in over a century, combining efficient heat pumps with cutting-edge artificial intelligence to create a sustainable home climate experience that is ten times better than traditional systems. Our efforts have attracted over $63 million in investments from esteemed firms such as Energy Impact Partners, Galvanize Climate Solutions, Lowercarbon Capital, and Gradient Ventures.The RoleAs we scale across North America, Quilt seeks a dedicated Controller to strengthen our financial infrastructure. In this pivotal leadership role, you will oversee the accounting function from start to finish, reporting directly to the CFO. Initially, you will engage in hands-on activities to establish processes and controls for our high-growth hardware and software business, preparing the company for its inaugural financial audit. As we expand, you will also build and lead the accounting team to support ongoing growth.What You’ll OwnLead the accounting function, ensuring compliance and accuracy in financial reporting.Develop and implement robust financial processes and controls.Collaborate with cross-functional teams to drive financial strategy.Prepare for and assist in the company's financial audit.

Riot Games is looking for a Manager, Software Engineering to guide the Tools & Frameworks team within the Developer Connections group. This team creates internal tools and frameworks that help other development teams work more efficiently. What you will do Lead and support engineers building developer productivity tools and frameworks Foster collaboration and encourage sharing of knowledge across the team Promote creative problem-solving and drive technical innovation Oversee engineering projects from initial planning through to delivery Locations Los Angeles, USA Mercer Island, USA Redwood City, USA

Revolution Medicines, Inc. is seeking an experienced and passionate Director of Clinical Quality to spearhead our quality assurance initiatives within our clinical operations. This pivotal role will focus on developing and implementing quality systems that ensure compliance with regulatory requirements and enhance the overall integrity of clinical trials. The ideal candidate will possess a strong background in clinical quality oversight and a commitment to driving continuous improvement in quality standards.

For over 25 years, Corcept Therapeutics has been dedicated to understanding cortisol, a critical hormone linked to a variety of diseases when not properly regulated.Our commercial portfolio features innovative treatments for hypercortisolism and oncology. With over 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists developed, Corcept is actively advancing clinical trials for conditions such as hypercortisolism, solid tumors, ALS, and liver disease. We are harnessing cortisol modulation to tackle some of the most challenging health issues faced by patients today.Headquartered in Redwood City, California, Corcept invites you to explore more about our mission and offerings at www.corcept.com.The Corcept Quality Systems Technology (QST) leader will be primarily responsible for evaluating Veeva Quality software projects and prioritizing critical initiatives for the QA department and Corcept. This role demands a strategic thinker who collaborates across functions to achieve mutual objectives, justifies software projects, and sets a clear path forward. The leader should be adept at managing complex system projects, supporting validation efforts as necessary, and overseeing project execution while ensuring strategic alignment.The ideal candidate will demonstrate the ability to convert business growth and increasing complexity into a cohesive software strategy, including a two-year framework that promotes sustained growth and organizational maturity. Projects will encompass new implementations, software enhancements, and ongoing process improvements.