Controller

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 com…

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.

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.

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 the Dexterity Team!At Dexterity, we envision a world where robots enhance human potential. Our cutting-edge technology liberates individuals to focus on creative, problem-solving tasks by allowing robots to take on repetitive and physically demanding jobs.We are pioneering warehouse automation, addressing the urgent need for smarter, more resilient supply chains that impact millions globally. Our full-stack robotic systems excel in picking, moving, packing, and collaborating with a human-like finesse, awareness, and learning capabilities. Driven by software and hardware-agnostic solutions, we have already successfully handled over 15 million goods in production. Our commitment to customer satisfaction is unwavering; every decision is guided by our mission to empower customers through the capabilities of robotics.Recognized as one of the fastest-growing companies in the robotics industry, we are supported by esteemed investors like Kleiner Perkins, Lightspeed Venture Partners, and Obvious Ventures. Our diverse, multidisciplinary team thrives on a culture of passion, trust, and commitment to innovation. Be a part of Dexterity and help us make intelligent robots a reality!

About Hammerhead AIAt Hammerhead AI, we are pioneering the future of artificial intelligence through advanced orchestration that addresses critical challenges in AI's access to power. Our innovative platform enhances data center power infrastructure, enabling maximum AI token generation within existing electrical constraints, all without necessitating new power plants or grid extensions. With over 8 gigawatts of mission-critical power optimized globally, we are tackling a staggering $64 billion annual market opportunity while significantly lowering the environmental impact of AI infrastructure.As part of our team, you will: Engage at the forefront of AI, energy, and computing to shape the next generation of AI infrastructure. Collaborate with industry experts specializing in modern Reinforcement Learning (RL), AI, IoT, and IIoT technologies. Play a vital role in creating a more sustainable future for AI computing. Join a trailblazing company redefining modern data center design and operations. Enjoy competitive compensation, equity, and benefits within a high-growth, mission-driven environment. Gain insights from a seasoned team with a history of building and selling successful startups.

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.

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 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.

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.

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.

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 by mutations in the RAS signaling pathway. The Manager of Document Management in Analytical Development & Quality Control is based in Redwood City, California. This role oversees the entire lifecycle of controlled documents within Analytical Development and Quality Control (ADQC), supporting both regulatory compliance and internal quality standards. The position manages documentation for internal teams as well as external partners. Key Responsibilities Oversee creation, review, approval, issuance, and archiving of controlled documents, including SOPs and work instructions. Develop and maintain document management practices and change control processes to meet regulatory and industry standards. Collaborate with cross-functional teams to assess, prioritize, and manage change requests. Track, document, and close change controls, including conducting impact assessments and obtaining required approvals. Communicate changes and their implications to stakeholders, such as senior management and regulatory affairs. Lead meetings across departments to keep documentation accurate and current. Monitor document metrics, identify trends, and highlight areas for improvement. Continuously evaluate and refine document management processes to enhance efficiency and effectiveness. Requirements Strong experience in the pharmaceutical or biotech sector. Background in document management, quality control, and regulatory compliance.

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.

About Dyna Robotics:At Dyna Robotics, we are at the forefront of robotic innovation, creating versatile robots fueled by our proprietary embodied AI foundation model. This model not only generalizes but also continuously enhances its capabilities across diverse environments, delivering commercial-grade performance. Our robots have successfully been implemented across various sectors, setting industry standards with unparalleled generalization and performance.Founded by seasoned entrepreneurs Lindon Gao and York Yang, who previously sold Caper AI for $350 million, along with former DeepMind research scientist Jason Ma, Dyna Robotics has raised over $140 million from top-tier investors, including CRV and First Round. We are on a mission to revolutionize the robotic automation landscape. Join us and contribute to shaping the future of AI-driven robotics!Discover more at dyna.coPosition Overview:As a Controls Research Engineer at Dyna Robotics, you will play a pivotal role in maximizing the potential of our robots' actuators. Your expertise will guide the design, testing, and deployment of advanced control algorithms that utilize comprehensive data to achieve the most dynamic movements. You will also be instrumental in developing tools that simplify controls research and enhance team understanding of how control impacts overall robot performance. Collaboration with robotics engineers, AI researchers, and hardware engineers will be essential to ensure the utmost efficiency in our systems.

Company Overview:Dyna Robotics is a pioneering force in the robotics industry, developing versatile robots that leverage our proprietary embodied AI foundation model. This technology allows our robots to adapt and enhance their capabilities across diverse environments, delivering commercial-grade performance that is unmatched in the sector. Our robots are already making significant impacts across various industries, demonstrating exceptional generalization and performance with our groundbreaking frontier model.Founded by visionary entrepreneurs Lindon Gao and York Yang, who successfully sold Caper AI for $350 million, alongside former DeepMind researcher Jason Ma, Dyna Robotics has secured over $140 million in funding from prominent investors like CRV and First Round. We aim to redefine robotic automation and invite you to join us in shaping the future of AI-driven robotics!Discover more about our innovative journey at dyna.coPosition Overview:As a Senior Robotics Software Engineer at Dyna Robotics, you will take a lead role in the design and development of advanced software solutions that interface seamlessly with our state-of-the-art robotic systems. Your expertise will guide the creation of software for robot control, sensing, and teleoperation, while also crafting tools for remote operation, data collection, and processing. You will collaborate closely with our AI research and hardware teams to bolster the intelligence and reliability of our robotic innovations, contributing significantly to our mission of achieving long-term general intelligence in robotic systems.