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A World-Changing Company Palantir builds the world's leading software for data-driven decisions and operations. By bringing the right data to the people who need it, our platforms empower our partners to develop lifesaving drugs, forecast supply chain disruptions, locate missing children, and more. The Role Palantir Technologies is seeking a Quality Compliance Manager to support our rapidly growing life sciences business. You will build and improve Palantir's Quality Management System (QMS) framework. You will enable Palantir's QMS to meet regulatory requirements and support change and innovation. You'll drive improvements to GxP quality systems and processes such as Change Control, Document Management System, Training, Deviation and CAPAs, as well as the tracking/trending/reporting of QMS Metrics. You will work closely with other functional departments within Palantir. Our ideal candidate is self-motivated and drives change across key areas of the business. You will also need to be innovative, collaborative, and receptive to feedback. The role and its surrounding organization aren't rigidly defined, so it's important that you can navigate an unstructured environment to fulfill critical business initiatives. Being able to develop interpersonal relationships with stakeholders across various teams will be key to being successful in this role. It will entail influencing existing processes by suggesting and driving change to champion QMS first principles. Ultimately, you will drive the vision and direction of Palantir's QMS. This is an opportunity to build something that will scale and support Palantir. Core Responsibilities Continue to develop a Palantir-wide QMS that lives under ISO 9001 and drives consolidation of process documentation and promotes process consistency at Palantir. Author and ensure implementation of approved procedures across the organization, setup non-conformance and CAPA processes to monitor deviations and management reporting. Establish inter-departmental relationships to achieve key results. Be the champion and advocate for ingrained QMS across Palantir, work with product development and product reliability teams to implement GxP processes. Enhance quality culture at Palantir. Support life sciences sales cycle, support customer and FDA audits regarding Palantir's Quality Management System, and complete assessment questionnaires for Life Sciences clients. Support Implementation of internal applications/systems supporting QMS processes like Document Management System and Learning Management System. Develop a Palantir-wide QMS that lives under 9001 and drives consolidation of process documentation and promotes process consistency at Palantir. Collaborate with software development teams to integrate quality and compliance considerations into product design and development processes. Develop and deliver training programs on quality management and ISO 9001 compliance to all relevant employees. What We Value Experience documenting SOPs and coordinating cross-functionally to maintain adherence to documented process. Experienced in building and running a Quality Management System and process areas within a QMS (e.g. Doc Control, Training, Supplier Management CAPA, SDLC, Change Control, etc.). Thrives in a fluid, dynamic and fast-paced environment, specifically a modern SaaS company. Ability to connect and develop positive relationships with employees across cross-functional teams (engineering, compliance, product reliability, product development, among others). Experience in demonstrating value proposition of a Quality System to internal stakeholders without experience/buy-in. A visionary who has no problem getting their hands dirty and doing the work necessary to create and improve the state of the world. What We Require You have at least 5+ years of relevant work experience. Strong understanding of ISO