Company Overview:

Beam Therapeutics is committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform that includes a suite of gene editing and delivery technologies and is in the process of building 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 potential 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:

The Senior QC Analyst / QC Analyst, Analytical Methods will support critical analytical method implementation workstreams in support of the facility start-up plan. These workstreams include analytical instrument qualification, critical reagent management, execution of technical protocols, and supporting the implementation of programs and procedures in a Quality Control laboratory located in Durham, North Carolina.

Responsibilities:

• Maintain and operate analytical instrumentation for flow cytometry and other bioassays
• Analyze data; interpretation of data within given parameters
• Investigate out of specification or unexpected results and study outcomes
• Escalate and assist in the resolution of complex issues
• Independently develop, author, and execute protocols, reports and other related documents
• Communicate effectively with peers, and demonstrate collaboration across different functions
• Draft and review technical documents

Qualifications:

• Bachelor’s degree required, preferably in a life science discipline.
• 2 years relevant experience.
• Expertise in leading the transfer and validation of analytical methods from research to implementation in a GMP environment, ensuring that routine sample testing will be compliant. Previous experience writing protocols and reports, training and guiding second analysts in the execution of testing to maintain consistency and compliance.
• Experience with implementing and qualifying new laboratory equipment in GMP settings, supporting smooth integration and compliance.
• Strong ability to collaborate with analytical research teams, ensuring successful method transfers and supporting continuous improvement initiatives.
• Hands-on experience with various analytical techniques primarily flow cytometry.
• Scientific knowledge of analytical method transfer requirements and processes.
• Technical writing skills.
• Ability to work independently in a high-paced team environment, meet deadlines, and prioritize.
• work from multiple projects.
• Advanced ability to communicate effectively with peers, department management and cross-functional peers.
• Must be able to work onsite daily and willing to have a flexible schedule during peak times, which may include supporting critical operations outside of normal work hours, as needed.