The Director of Pharmacovigilance at Beam Therapeutics will oversee safety monitoring and pharmacovigilance activities for assigned products, ensuring compliance with regulations. Responsibilities include managing safety reports, facilitating safety meetings, assessing safety signals, and collaborating with cross-functional teams. The role requires strategic planning, operational support, and development of safety documentation.

The Lead IT Technical Analyst, MES Systems is responsible for implementing and supporting Beam's Manufacturing Execution System, leading integration efforts, and providing ongoing IT support for manufacturing operations. The role involves technical leadership in system administration, project management, and business process improvement, ensuring compliance with GxP standards.

The Director of mRNA Process Development will lead the development, optimization, and scale-up of mRNA manufacturing processes. This role entails guiding a team of scientists, managing quality standards, and working cross-functionally to mitigate risks while ensuring operational excellence.

The Associate Director, Analytical Research & Development will lead a team developing and optimizing analytical assays for plasmids, oligonucleotides, and lipid nanoparticles. The role involves collaboration with process and formulation teams, ensuring compliance with ICH guidelines and cGMP regulations while overseeing routine in-process testing support and providing technical guidance.

The VP of Product and Portfolio Strategy for Genetic Diseases will lead the product strategy and commercialization pathway for Beam's liver portfolio, focusing on innovative therapies like BEAM 302. Responsibilities include overseeing lifecycle management, formulating commercial strategies, and collaborating with cross-functional teams to deliver on development goals and market readiness.

The Specialist/Sr. Specialist will enhance the Quality Management System (QMS), ensuring compliance with GxP standards while collaborating with Veeva and managing supplier qualifications. Key responsibilities include reviewing QMS records, preparing for regulatory inspections, driving continuous improvements, and providing data for management reviews, contributing to quality initiatives across Beam's operations.

The Associate Director of LNP Development at Beam Therapeutics will oversee the late-stage product development of lipid nanoparticles, collaborating with various departments to advance the pipeline. Responsibilities include contributing to CMC strategies, leading technology transfer projects, and generating data for regulatory filings. The role requires expertise in drug product development and a strong understanding of regulatory processes.

The Director of Control Strategy in Analytical Development at Beam Therapeutics will lead efforts to develop and document analytical control strategies for late-stage molecules. Responsibilities include proposing integrated processes, applying QbD and ICH guidelines, analyzing data for presentations, and ensuring compliance with cGMP. The role demands deep understanding of analytical methods and significant experience in the pharmaceutical industry.

The IT Technical Analyst will support Beam Therapeutics' Quality Systems with a focus on Veeva Quality Suite. Responsibilities include gathering business requirements, implementing application modules, configuration, testing, and providing operational support while partnering with stakeholders for continuous improvement efforts.

The Quality Control Analyst will support analytical method implementation in a QC laboratory, including maintaining analytical instrumentation, analyzing data, resolving issues, and drafting technical documents while collaborating with other functions. The role requires hands-on experience with analytical techniques and effective communication skills.

The Director of Pharmacovigilance will provide strategic scientific and operational support for pharmacovigilance activities, oversee safety reports, lead signal management and process development, and collaborate with various departments to ensure compliance and efficient operations in product safety monitoring.

The Quality Control Specialist will serve as a Subject Matter Expert (SME) in the QC group, focusing on method implementation for GMP testing, training junior analysts, managing laboratory operations, and ensuring compliance through detailed data analysis and documentation. The role requires collaboration across departments to ensure timely project completion.

The Quality Control Analyst will execute various analytical methods to evaluate in-process samples and support cGMP manufacturing operations, including instrument maintenance, data documentation, and cross-functional communication. The role requires maintaining daily lab operations and supporting continuous improvement initiatives.

The Director of Marketing and Commercial Network Operations will optimize the delivery of BEAM-101 to Treatment Centers for Sickle Cell Disease, ensuring effective communication and collaboration across teams. Responsibilities include defining strategies for onboarding centers, setting operational delivery metrics, and generating insights for process improvement, particularly in the gene therapy sector. The role requires cross-functional coordination and the ability to adapt strategies based on evolving industry trends.