Beam Therapeutics Job Trends

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...

Beam is seeking a talented and experienced Senior Corporate Counsel, Corporate and Securities to join our growing legal team. This is a rare opportunity a senior legal role with genuine breadth at a company where your judgment, perspective, and voice will have a meaningful impact. Reporting to the Senior Vice President, Legal Affairs, you will structure and negotiate the collaborations and licensing transactions that advance our pipeline, take a leading role in SEC reporting and corporate governance for a public company, and advise senior leadership directly. You will partner closely with business development, alliance management, finance, investor relations, and human...

Beam is looking for a highly energetic Sr. Engineer II / III, Automation and MES with GMP manufacturing experience focused on design, installation, configuration, maintenance support, and validation of Rockwell PharmaSuite system. Additionally, the role will support other automation systems including DeltaV, PI, and Igniton. The candidate will be a core team member for the Engineering and Facilities team developing and maintaining automation systems at the new multi-modality site in Durham / RTP, NC. This is a fantastic opportunity to help continue to develop and grow Beam manufacturing and automation long -term strategy. The successful candidate will show initiative in...

Beam isseekinga highly talentedand motivatedengineering or science studentinterested ina career in biopharmaceutical manufacturingto join our Technical Operationsteamfrom January through June 2027 as a co-op.The Technical Operations co-op willbe responsible forsupporting thecross-functional validationteamsthatdemonstratenewly developedgene editingequipment andmanufacturing processeswork as intendedby Beamandasrequired bygovernment agencies (includingFDA) for thebenefit of patients.Supportactivitieswill includelearning aboutandobtainingscientific/technical informationrelated to manufacturingequipment andprocessesto ensureintegrity of dataincluded in Technical Operations protocols and reports.As a part of thesecross-functionalteams, the candidate will have the opportunity tointeractwithvarious functions involved with supportingthebiopharmaceutical manufacturingindustry, including R&D(process and analytical development),Manufacturing, Manufacturing Sciences and Technology (MSAT),Quality (both Quality Control and Quality Assurance), Supply Chain, and Procurementto help the...

Beam is looking for a Director, Patient Services, to join our growing Market Access team. The Director, Patient Services will lead development and execution of the patient services strategy for risto-cel, Beam’s lead asset in development for sickle cell disease. Responsibilities Lead patient services for risto-cel, including program design, operational planning, launch readiness, and execution. Develop practical patient support and reimbursement solutions that support brand strategy and overcome access barriers. Partner with Brand, Account Management, Field Market Access, Patient Advocacy, and Patient Operations to execute the Patient Services strategy. Use data and analytics to monitor program performance, identify...

The Director, FP&A (Clinical), will be a key member of the FP&A team reporting to the VP of FP&A. The focus of this position will be managing the planning processes and serving as the business partner to the Commercial organization and working cross-functionally to ensure accuracy of commercial revenue projections. This position will also be responsible for most financial modeling projects on the FP&A team and interact closely with the accounting team on the month end closing process. Responsibilities FP&A business partner to the Commercial, and risto -cel program. Oversee planning cycle activities and review and ensure accuracy...

The Director, FP&A (Commercial), will be a key member of the FP&A team reporting to the VP of FP&A. The focus of this position will be managing the planning processes and serving as the business partner to the Commercial organization and working cross-functionally to ensure accuracy of commercial revenue projections. This position will also be responsible for most financial modeling projects on the FP&A team and interact closely with the accounting team on the month end closing process. Responsibilities FP&A business partner to the Commercial, and risto-cel program. Oversee planning cycle activities and review and ensure accuracy of plan...

The Regulatory Director/Sr. Director Regulatory CMC will be responsible for preparing CMC and Quality related health authority agency correspondence and regulatory applications, as well as govern CMC submissions and regulatory compliance support for the development of global products. This position will lead regulatory activities to support high quality CMC sections of regulatory documentation. Responsibilities Provide regulatory CMC strategic leadership within Regulatory and on cross-functional teams to support development of innovative genomic medicines/ex-vivo and in-vivo therapies. Develop and proactively communicate regulatory CMC strategies, risks and key issues in an evolving regulatory landscape. Act as the regulatory CMC lead and department...