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The QA Document Control Specialist manages and maintains controlled documents within an electronic document management system to ensure compliance with global regulatory standards. Responsibilities include collaborating with cross-functional teams for document revisions, supporting compliance audits, and training staff on eDMS and document control processes.
The Director of Alliance Management is tasked with building partnerships with pharmaceutical companies to enhance their research using Tempus products. Responsibilities include managing data operations, providing scientific support, improving client satisfaction, and addressing partners' needs by developing customized proposals and cross-functional collaboration.
The Senior Supplier Quality Assurance Specialist will support quality activities related to Supplier Quality Management, ensuring compliance with FDA QSR and ISO 13485. Responsibilities include vendor approval, managing documentation, handling corrective actions, monitoring supplier performance, and maintaining supplier metrics.
The Senior Supplier Quality Assurance Specialist supports quality activities related to Supplier Quality Management in compliance with FDA and ISO regulations. Responsibilities include vendor approval, documentation management, supplier performance monitoring, and leading corrective actions based on supplier audits.
The Senior Manager of Quality Assurance oversees issue management processes related to compliance with FDA and ISO regulations. Responsibilities include managing nonconformance and corrective action systems, leading process improvements, collaborating with regulatory teams, and analyzing trends to prevent quality issues.
The Senior Business Intelligence Engineer will manage the design and administration of analytics dashboards, collaborate with stakeholders for data analysis, and develop data governance initiatives. Responsibilities include designing data views, performing root cause analyses, and participating in data projects lifecycle management.
The Quality Assurance Associate is responsible for documenting and tracking compliance for IVD medical devices and clinical laboratories. Key duties include maintaining quality records, aiding in audits, facilitating corrective actions, and managing onboarding processes. The role requires strong attention to detail and the ability to adapt quickly in a fast-paced environment.
The Senior Director of Marketing for Life Sciences is responsible for creating and implementing effective marketing strategies to promote Tempus’ solutions to Pharmaceuticals and Biotech companies. This role focuses on lead generation, revenue growth, and creating compelling narratives that convey the value of Tempus’ offerings, while collaborating across departments to align marketing efforts with business goals.
The Quality Assurance Specialist will oversee the certification processes for Tempus products, collaborate across multiple departments to ensure regulatory compliance, assist in audits, maintain QMS documentation, and provide strategies for process improvements. They will support inspections and audits and manage communication with regulatory bodies.
The Sales Operations Associate will support the strategic and operational aspects of Tempus' Life Sciences business. Key responsibilities include analyzing sales data for trends, maintaining sales dashboards, preparing reports for business reviews, and collaborating with teams to enhance sales strategies and operational efficiency.
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