About the role
Company Overview
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
Position Overview
Beam is looking for a highly energetic co-op to join our growing quality control team. The co-op will provide operational, administrative, and laboratory support to the QC organization. This role is intended to support PLI readiness, method lifecycle activities, laboratory organization, reagent traceability, and quality-system-related activities while providing hands-on exposure to a GMP-regulated laboratory environment.
Responsibilities
Assist in procurement, tracking, and management of reagents and materials. Assist with method lifecycle activities, including feasibility runs and troubleshooting of analytical methods and laboratory instruments under supervision. Organize, document and archive historical data sets. Support quality event documentation (e.g., Deviation, CAPA, Change Control). Assist in reviewing data generated by other analysts to ensure accuracy and compliance. Learn about key functions in pharmaceutical development and manufacturing, including analytics, stability testing, manufacturing processes, and quality systems. Gain hands-on experience with ana
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