Senior Manager, Analytical Development & Quality Control

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 patient…

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.

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, 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.

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 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.

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.

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.

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

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.

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 Bellota Labs, a pioneering startup on a mission to transform the online gaming industry through our innovative product, ClubWPT Gold, developed in collaboration with the World Poker Tour. We are dedicated to enhancing game integrity and delivering unparalleled customer experiences. As a Senior/Principal Analytics Engineer, you will play a crucial role in shaping our data and analytics infrastructure, enabling informed business decisions across Finance, Marketing, Product, and Operations. Become part of a visionary team that is redefining the gaming landscape!

Join our team as a Senior Quality Engineer and play a pivotal role in enhancing the quality assurance processes within our organization. You will be responsible for developing and implementing robust quality standards, conducting thorough testing, and collaborating with cross-functional teams to ensure product excellence.

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.

Revolution Medicines is at the forefront of clinical oncology, dedicated to developing innovative targeted therapies for patients afflicted with RAS-addicted cancers. Our cutting-edge R&D pipeline features a range of RAS(ON) inhibitors aimed at targeting various oncogenic RAS protein variants, including daraxonrasib (RMC-6236), elironrasib (RMC-6291), zoldonrasib (RMC-9805), and RMC-5127, all currently advancing through clinical development. As a member of our dynamic team, you will join fellow professionals committed to making a meaningful impact on the lives of patients battling cancers linked to the RAS signaling pathway.The Opportunity:We are on the lookout for a seasoned clinical science drug developer to take on the role of Senior Director of Clinical Development, pivotal in supporting our clinical-stage molecules. In this essential position, you will oversee various clinical science deliverables, ensuring the effective execution of the clinical development plan for specific molecules within their respective indications. Your responsibilities will encompass early-stage clinical research through to pivotal studies, including regulatory submissions. You will play a crucial role in shaping the clinical science component of the Clinical Development Plan (CDP) strategy, driving the advancement of transformative therapies for patients.Lead the clinical science elements of the clinical development strategy and documentation.Represent the clinical development plans across relevant teams, ensuring effective training for study site personnel, acting as the main point of contact for inquiries related to the CDP at a program level, and overseeing medical/safety data reviews and study reporting.Potential assignment to complex and high-priority strategic studies for our molecules, with the expectation of exercising independent and self-directed leadership.Align cross-functionally with scientific, regulatory, and commercial objectives while executing the clinical development plan.Lead, mentor, and contribute to a high-performing cross-functional team of clinical development professionals, fostering a culture of collaboration, innovation, and excellence.Oversee all facets of clinical trial design and execution, including site selection, patient recruitment, data management, and regulatory compliance.

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.

WHAT IS BOX?Box Inc. (NYSE:BOX) is at the forefront of Intelligent Content Management. Our innovative platform empowers organizations to enhance collaboration, oversee the entire content lifecycle, secure vital information, and revolutionize business workflows through enterprise AI. We assist companies in thriving in this era dominated by AI. Since our inception in 2005, Box has streamlined operations for top global firms, including JLL, Morgan Stanley, and Nationwide. With our headquarters based in Redwood City, CA, and offices strategically located across the U.S., Europe, and Asia, we are dedicated to transforming how businesses operate.Joining Box means you will play a pivotal role in advancing our platform. Content is the lifeblood of professional environments, comprising the myriad files and information exchanged daily: contracts, invoices, employee records, financial statements, product specifications, marketing assets, and much more. Our ambition is to infuse intelligence into content management and empower our clients to completely revamp their workflows. With the synergy of AI and enterprise content, the potential to redefine collaborative work has never been more significant, and you will be at the forefront of this monumental transformation at Box.WHY BOX NEEDS YOUThe Developer Relations team at Box is passionate about inspiring and equipping developers to create the next generation of intelligent, content-driven applications. We are seeking a Developer Relations Engineer to enhance developer awareness and engagement, ultimately driving adoption that leads to pipeline creation. You will represent Box within developer communities, at conferences, and across various content platforms. Your role will not only involve producing content but also measuring what drives engagement and optimizing strategies accordingly. The domain of content-driven AI workflows is an emerging landscape without a predefined blueprint—you will help shape how developers discover and engage with this exciting field.Your primary objective will be to enhance developer awareness. The responsibilities outlined below are our current thoughts, but we encourage you to challenge, refine, and evolve these strategies as you learn what resonates. The crucial metric is developer reach and interest; the methods you employ to achieve this are yours to define. When developers consider content within their AI workflows, Box should be top of mind.WHAT YOU'LL DOContent Creation: Develop demonstrations, author technical blog posts, lead webinars, and produce video content. Collaborate with engineering teams for technical accuracy; you will own the content output.Events and Engagement: Participate in and speak at developer and AI engineering conferences. Control the event strategy, cultivate relationships with organizers, and partner with industry leaders.

Join Revolution Medicines, Inc. as a Senior QA Manager, where you will play a pivotal role in leading our Quality Assurance efforts for Good Clinical Practices (GCP) and Good Manufacturing Practices (GMP) compliance. You will be responsible for conducting audits, ensuring adherence to regulatory requirements, and fostering a culture of quality within our organization. This role demands a strategic thinker with a strong background in quality assurance and regulatory compliance.

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.

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.