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The Associate Director oversees compliance reporting for the US Transparency Program, ensuring accurate data collection and regulatory adherence while leading cross-functional collaborations and continuous process improvements.

The Clinical Study Associate Manager oversees clinical trial delivery, ensuring compliance with regulations and effective collaboration with vendors. Responsibilities include planning, risk assessment, monitoring data quality, and managing study-related tasks and reports.

The Associate Director, Thought Leader Liaison will engage with oncology thought leaders, enhancing business discussions and implementing strategic initiatives within the Oncology Solid Tumor portfolio.

The Quality Control Scientist will validate microbiological test methods, ensure compliance with regulations, support aseptic processes, and assist in technical documentation and investigations.

The Clinical Study Associate Manager oversees the planning and management of clinical trials, ensuring compliance with regulations, fostering vendor relationships, and monitoring study progress while contributing to risk assessments and documentation.

The Executive Director, Neurology Marketing, leads commercialization efforts for Neurology brands, focusing on strategy, growth, and cross-functional collaboration globally, particularly for Myasthenia Gravis.

Lead QA Technical Operations for clinical and commercial biologics manufacturing: define cGMP standards, oversee QA MES, validation oversight, and tech transfer; ensure audit readiness, present quality metrics, allocate QA resources, and maintain regulatory compliance.

Lead and manage IT/OT operations in a GxP-regulated environment, ensuring reliable infrastructure (servers, networking, WiFi), compliance with FDA standards, integration of IT and OT systems, vendor management, disaster recovery, and performance reporting while mentoring a technical team.

Lead scientific marketing activities for Myasthenia Gravis, focusing on promotional strategies, KOL engagement, and educational programs.

Lead design and deployment of a regulated QC lab orchestration layer connecting instruments, middleware, and enterprise systems. Define integration patterns, ensure scalability, resilience, and data integrity (GxP/21 CFR Part 11/Annex 11). Translate QC processes into automated workflows, enable sample lifecycle automation, evaluate vendors, support validation and incident resolution, manage budgets and vendor relationships, and drive the connected lab roadmap.