Requirements Required: High school diploma or equivalent; Experience in manufacturing operations; Experience working in a cGMP-regulated environment; Hands-on experience using hand tools; Proficiency with computers, including word processing, spreadsheets, and web-based applications; Ability to follow SOPs, maintain accurate documentation, and recognize deviations; Strong attention to detail, accountability, teamwork, and communication skills; Ability to work onsite in Devens, MA, on the specified rotating overnight schedule; Authorization to work in the United States without visa sponsorship. Preferred: Bachelor's degree in Science, Engineering, Biochemistry, or a related discipline; Experience with biopharmaceutical manufacturing equipment, including bioreactors or media and buffer preparation systems; Familiarity with DeltaV, Syncade, or OSI/PI Historian; Familiarity with SAP, Vault, or Maximo; Experience working in cleanroom environments.