Quality Control Specialist

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 impro…

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 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.

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.

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.

About Corcept Therapeutics Corcept Therapeutics has spent more than 25 years advancing the science of cortisol. This hormone plays a central role in many diseases when its regulation is disrupted. The company develops treatments for hypercortisolism and oncology, with a portfolio that includes over 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. Ongoing clinical trials target conditions such as hypercortisolism, solid tumors, ALS, and liver disease. Corcept is based in Redwood City, California. More information is available at www.corcept.com. Role Overview: Quality Systems GxP Training Specialist II This position supports the Quality Systems team by strengthening the GxP training program. The specialist works with systems like ComplianceWire to manage training compliance and is responsible for evaluating issues and recommending solutions independently. The role reports to the Sr. Manager of Document Control and GxP Training. Location Redwood City, California, United States

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.

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 our dynamic team at Adverum Biotechnologies, where we are dedicated to developing innovative gene therapies to treat patients with serious diseases. We are seeking a passionate and detail-oriented Quality Assurance Operations Specialist III to support our QA operations. This is a contract position that offers an exciting opportunity to contribute to our mission of improving patient outcomes through cutting-edge biotechnology.

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

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.

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.

Join Revolution Medicines, a pioneering late-stage clinical oncology company dedicated to developing innovative targeted therapies for patients suffering from RAS-addicted cancers. Our cutting-edge R&D pipeline features RAS(ON) inhibitors aimed at targeting various oncogenic variants of RAS proteins, including daraxonrasib (RMC-6236), elironrasib (RMC-6291), zoldonrasib (RMC-9805), and RMC-5127, all currently in clinical trials. As part of our dedicated team, you will collaborate with top-tier professionals committed to improving the lives of patients impacted by mutations in the RAS signaling pathway.The Opportunity:The Associate Director of Good Laboratory Practice Quality Assurance (GLP QA) will play a vital role in ensuring compliance with GLP standards at Revolution Medicines and its external vendors engaged in regulated activities.Your responsibilities will encompass overseeing GLP compliance for research laboratory vendors supporting regulatory clinical studies.You will develop and implement the annual vendor audit plan.You will conduct and manage vendor audits, including:Creating the audit plan, executing audits, and compiling reportsCoordinating audit closure tasks and reviewing vendor responses in collaboration with operational subject matter experts as necessaryProviding recommendations for vendor approvalsMaintaining vendor approval statuses in Veeva.You'll also participate in internal audits.Your role includes providing QA reviews of CRO study protocols and reports for compliance, employing a risk-based approach, and advising Nonclinical Development and Clinical Pharmacology (NDCP) teams on compliance matters.Monitoring vendor QA units to ensure adherence to applicable regulations, including reviewing vendor-specific QA audit reports.Advising sponsors on compliance requirements for test and control articles used in GLP studies.Collaborating and consulting with GLP vendor QA departments on study-related compliance issues.

Join us as a Quality Engineer at Collabera Inc., where you will play a crucial role in ensuring the highest standards of quality in our products. You will be responsible for designing and implementing testing procedures, identifying defects, and collaborating with cross-functional teams to enhance product performance.

Revolution Medicines, Inc. is seeking an experienced Associate Director of Global Quality Systems and Compliance to lead our quality management efforts. In this pivotal role, you will be responsible for developing and implementing quality systems that ensure compliance with regulatory standards and best practices. Your expertise will guide the organization in maintaining the highest quality standards across our operations, fostering a culture of continuous improvement.As a key member of our leadership team, you will collaborate closely with cross-functional teams to drive compliance initiatives, conduct audits, and ensure that all quality processes align with industry regulations. Your strategic vision and leadership will be instrumental in shaping our quality compliance roadmap.

Join Revolution Medicines as a Quality Assurance Intern and contribute to our mission of advancing transformational medicines for patients with cancer. As an integral part of our dynamic team, you will gain hands-on experience in quality assurance processes, helping to ensure the highest standards of product quality and compliance.

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.

About PoshmarkPoshmark stands as a premier fashion resale marketplace, driven by a dynamic and engaged community of buyers and sellers, complemented by real-time social experiences. Our platform is designed to transform the online selling experience into an enjoyable, social, and straightforward process. Since our inception in 2011, we have empowered sellers to turn their closets into flourishing businesses while sharing their unique styles with the world. With a thriving community of over 130 million users and more than $10 billion in Gross Merchandise Volume (GMV), Poshmark has enabled sellers to earn billions, delighting buyers with exceptional deals and unique items, all while promoting a sustainable future for fashion. For further details, visit www.poshmark.com and for company news, visit newsroom.poshmark.com. About the RoleWe are on the lookout for a dedicated Software Quality Assurance Engineer to join our expanding Quality Assurance team. In this pivotal role, you will play a key part in ensuring the reliability, performance, and quality of Poshmark’s mobile, web, and cloud platforms. This hands-on position will allow you to contribute to the enhancement of our QA processes, methodologies, and best practices.This is an exhilarating opportunity for a meticulous QA professional who thrives on addressing complex challenges, collaborating across various departments, and pursuing professional growth in a fast-paced product environment. Key ResponsibilitiesConduct manual QA testing for both new and existing features across:iOS and Android mobile applicationsWeb applicationsCloud platform servicesExecute end-to-end, functional, and performance testing to guarantee product quality and stabilityCreate detailed test scenarios and test cases based on business requirements, user stories, and design documentationIdentify, document, and manage defects using bug tracking tools (JIRA preferred)Analyze issues, conduct root cause analysis, and assign defects to the appropriate development teamsWork collaboratively with Engineering and Product teams to ensure prompt resolution of issuesReview bug reports, functional requirements, and technical designs to continuously enhance test coverageParticipate in regression testing cycles and aid in maintaining test quality across releases