Beam Therapeutics Job Trends

Beam is seeking a highly talented and motivated Associate-level operations professional to join our growing Laboratory Operations team. This role will be responsible for contributing to all aspects of lab operations and facility support for both R&D and GMP environments. As this is a cGMP-facing role the successful candidate will have direct, hands-on experience working within a regulated cGMP manufacturing or GMP laboratory environment and will be expected to execute all activities in accordance with cGMP, Good Documentation Practices (GDP), and ALCOA+ data integrity principles. The Associate will serve as a day-to-day user and data steward of the site Computerized...

Beam is looking for a highly motivated, strategic and driven commercial leader to join our growing Hematology Franchise. The Senior Director / Vice President, Hematology Marketing will drive brand strategy development, commercial launch readiness and execution for Beam’s lead asset, Risto-cel, an ex vivo autologous hematopoietic stem cell-based gene therapy for the treatment of severe sickle cell disease (SCD). This is a high impact role for Beam’s potential first product commercialization. The successful candidate plays a critical role in leading the marketing and marketing operations team. The Senior Director / Vice President, Hematology Marketing , reports into the SVP,...

Beam is seeking a Senior IT Business Analyst, G&A to support technology solutions across the General and Administrative departments in a rapidly growing organization. This person will support Beam’s G&A Enterprise Application portfolio which is comprised of Financial, Operational, Legal and Human Resources solutions. This role is critical in providing implementation support for new systems and production support for all G&A stakeholders. Responsibilities Serve as the Senior Business Analyst on projects for new implementations and system enhancements, working with internal stakeholders and vendors to ensure technical solutions meet Beam’s needs. Build a collaborative relationship with stakeholders to proactively identify business...

Beam is looking for a highly motivated and detail-oriented Manufacturing Sciences & Technology Co-op to join our Technical Operations organization from January through June 2027 . This role offers an opportunity to gain hands-on experience supporting late-stage clinical cell therapy manufacturing operations through projects focused on aseptic process simulation (APS), process validation, and regulatory inspection readiness. Under the guidance of under the guidance of their mentor, the co-op will support strategic initiatives that strengthen process understanding, sterility assurance, and manufacturing process robustness while collaborating across Manufacturing, Quality, Validation, and Technical Operations functions. Responsibilities Develop a project plan, define objectives...

The Associate Director/Director in Clinical Pharmacology position will support a rapidly expanding clinical portfolio of promising gene/base editing therapeutics. The candidate in this position should have strong scientific and technical skills , be well versed in PK and PD with a strong ability to critically evaluate and interpret data, conduct rapid exploratory analysis, quantitative systems pharmacology (QSP) and PKPD modeling. In this role, the candidate is expected to have strong data analyses, modeling, and critical thinking ability with good oral and written communication skills. The role could be tailored to focus solely on pharmacometrics or could be a hybrid Clinical...

We are building a best‑in‑class Field Medical organization as a natural next step in the growth of our Medical Affairs organization at Beam therapeutics! This Director level MSL will own a defined US territory with primary responsibility in sickle cell disease (SCD) and shared accountability across the Beam pipeline, including Alpha‑1 antitrypsin deficiency (Alpha‑1) and glycogen storage disease 1a (GSD). You will architect territory strategy, onboard priority treatment centers, engage KOLs and HCPs, generate actionable insights, and drive pre‑commercial launch readiness in close collaboration with cross‑functional partners. Responsibilities Develop and execute territory strategy map treatment centers, referral networks, transplant/infusion sites,...

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...

The QC Senior Analyst, Raw Materials will support QC Raw Material Program and Testing activities, including onboarding materials, conducting raw material risk assessments and execution of daily operations in the QC laboratory. This position is responsible for QC sampling, testing and release of incoming raw materials, components and biological materials used in the production process per established procedures. The role will also support oversight and review of contract testing of raw materials. Responsibilities Perform QC sampling, testing and release of incoming raw materials, reagents and components. Support onboarding and qualification of materials and components by creating risk assessments and material...

Beam is seeking a dynamic and detail-oriented Human Resources Co-Op to join our team from January through June 2027. The Human Resources Co-op will support key HR initiatives and projects focused on strengthening HR operations, processes, and compliance. This role will provide hands-on experience reviewing HR processes and documentation, identifying opportunities for improvement, and supporting efforts to strengthen consistency and compliance across HR practices. The co-op will collaborate with HR and cross-functional stakeholders while building practical experience in HR operations, project management, and process improvement. Responsibilities Review HR processes and personnel files to assess alignment with applicable regulatory requirements,...

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...

The Associate Director of Product Quality Assurance (PQA) will be responsible for phase appropriate quality oversight of internal and external manufacturing and analytical activities. These activities include analytical testing performed by Beam staff in Cambridge as well as that performed by external partners at contract test labs. Oversight of internal analytical instrument and method qualification/validation is also in scope. Additionally, manufacturing of various products at our CDMOs/external partners is managed as part of this role. The position will be critical to the overall build strategy and growth of the Quality organization for Beam as the company grows and evolves from...

We are seeking an experienced Process and Cleaning Validation subject matter experts to provide Validation support and leadership for development of the process and cleaning validation programs, strategies to be applied to early processes entering these validation programs, and expertise in validation project management and technical document preparation as needed. Key Responsibilities Design and implement approaches for validation studies, using knowledge and input from Process Development, Analytical Development, Manufacturing, MST/ENG, and Quality partners. Lead the development and execution validation master plans and/or project plans, protocols, and reports for process validation activities. Conduct risk assessments and gap analyses of existing validation...