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Job description
Manufacturing Technical SpecialistShift Details: The shift is 07:00AM -7:00 PM and it would be for A shift. The work week alternates between Monday, Tuesday, Friday, Saturday, Sunday, and Wednesday Thursday.Project Summary:The Manufacturing Associate Level I is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment.They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling products and materials.Accountabilities:Perform 6S and stock each suite daily, clean soiled parts daily.Determine production needs for autoclaved assembles and deliver to suites.Perform daily and weekly maintenance activities on analytical equipment.Perform weekly and monthly cleans of inoculum rooms.Report all activities in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.Attain qualification for all assigned tasks and maintain individual training planPrepare materials for transport and delivery to manufacturing suites. Perform material movements into, out of, and across the production areas.Maintain facility and equipment through routine cleaning and sanitization.Administrative tasks – attending suite shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.Perform other duties as assignedHigh School Diploma or Equivalent
Worksite address
portsmouth, NH, 03801, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.