About the role
This role manages Rockwell PharmaSuite MES systems supporting GMP manufacturing at Beam Therapeutics' new multi-modality cell therapy manufacturing site in Durham, NC, including designing electronic batch records, configuring master recipes, leading change control, and serving as the automation subject matter expert for clinical and commercial production.
Candidates need a BS in engineering or equivalent experience, 10+ years (Engineer I) or 12+ years (Engineer II) in automation/MES with demonstrated technical leadership, hands-on GMP MES platform experience (Rockwell PharmaSuite strongly preferred), and knowledge of computer system validation standards (GAMP 5, FDA 21 CFR Part 11, EU Annex 11). The role sits on Beam's Engineering and Facilities team, collaborating across manufacturing operations, quality, process development, IT, and supply chain.
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