Top Software Engineer Jobs

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 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.

Seek a director to lead the development of Tempus’ multi-modal molecular data model. Responsibilities include implementing scientific strategies for data usage, designing data models, and managing cross-functional projects. The role bridges scientific research and engineering practices to enhance the healthcare sector with AI-driven insights.

The Quality Engineer is responsible for implementing quality assurance principles for the development and maintenance of medical devices. This includes risk management, quality assurance reviews, documentation planning, participation in audits, investigations of quality events, and support in process validation and change management activities.

As a Senior Quality Engineer, you will lead the verification and validation of medical device systems, develop compliance documentation, manage risk assessments, and provide guidance in Computer System Validation, ensuring adherence to FDA regulations and industry standards. You'll engage in collaborative efforts, supporting quality assurance processes and training team members.