Engineer II/Senior Engineer I, Automation and MES

• Serve as the site subject matter expert for Rockwell FactoryTalk PharmaSuite MES, including configuration, master recipe and workflow authoring, exception handling, and defect triage.
• Lead the design, implementation, and lifecycle management of electronic batch records (EBR) for clinical and commercial cell therapy manufacturing processes, including phase design, calculations, transitions, CPP/process limits, and electronic signature flows.
• Convert paper master batch records into compliant, operator-friendly electronic execution in partnership with Manufacturing, MS&T, and Quality.
• Own MES change control end to end: impact assessment, requirement/functional/configuration specifications, test protocol authoring and execution (IQ/OQ/PQ), deviation documentation, and requirements traceability matrix support.
• Support MES system implementation and lifecycle, including system architecture, platform components, and interfaces to partner systems (SAP, LIMS, CMMS, PI, and patient logistics chain-of-identity / chain-of-custody systems).
• Support the deployment of PharmaSuite MES to new and existing suites, processes, and products as the site scales capacity across modalities.
• Support inspection and licensure readiness, including mock pre-license inspection runs, audit trail review, data integrity controls per 21 CFR Part 11 and EU Annex 11, and MES business continuity procedures.
• Provide floor-side support, hypercare, and operator training during go-live; translate operator feedback into practical recipe and workflow improvements.
• Support plant operations and troubleshoot automation issues, including participation in an on-call / after-hours support rotation for GMP manufacturing.
• Support development and lifecycle management of other automation systems, including DeltaV, PI, and Ignition.
• Develop and maintain requirement specifications, functional specifications, design specifications, and guidelines for automation and MES systems.
• As part of the engineering team, further develop and execute the long-range automation, MES, and digital manufacturing strategy.
• Provide technical expertise and assist in the execution of automation capital improvement and compliance projects, including suite buildouts and capacity expansion.
• Mentor junior engineers and contract resources, and document system knowledge so that critical MES expertise is shared across the team.
• Cultivate Beam’s culture and our values-driven organization, focused on our people.
• Ensure safety, quality, compliance, efficiency, and sustainability throughout our engineering, automation, and cGMP operations.

• BS degree in Engineering or a related technical discipline, or equivalent practical experience.
• Engineer II: typically 6+ years of relevant automation/MES experience. Senior Engineer I: typically 8+ years, including demonstrated technical leadership of an MES or automation program.
• Demonstrated hands-on experience with the design, configuration, testing, and deployment of a GMP MES platform. Rockwell PharmaSuite strongly preferred; Emerson Syncade, Korber PAS-X, Tulip, or Apprentice experience will be considered.
• Direct experience authoring, configuring, or validating electronic batch records and master recipes in a regulated manufacturing environment.
• Working knowledge of computer system validation and data integrity expectations (GAMP 5, FDA 21 CFR Part 11, EU Annex 11, ALCOA+).
• Experience in a biotechnology, pharmaceutical, or medical device manufacturing environment.
• Excellent organizational, verbal, and written communication skills, with the ability to communicate effectively within cross-functional teams and to management.
• Ability to work on multiple projects and manage various priorities and timelines, and to adapt quickly to changing circumstances.
• High degree of customer focus (internal/external) and demonstrated collaboration in a team environment.
• Results oriented, with the ability to demonstrate resiliency, ownership, and drive.
• Ability to manage commitments for self while displaying an eagerness to learn and continuously improve.

• Cell and gene therapy or autologous / patient-specific manufacturing experience, including chain-of-identity and chain-of-custody requirements.
• Experience supporting a BLA filing, pre-license inspection (PLI/PAI), PPQ campaign, or commercial go-live of a validated MES.
• Experience with MES-to-ERP integration (SAP), and with LIMS, CMMS, and historian (PI) interfaces.
• Experience with DeltaV, PI, and Ignition.
• Capital project, start-up, and manufacturing support experience.
• Previous experience with Agile or LEAN delivery methods.

The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.

$140,000—$185,000 USD

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.