Document Control Administrator - I (Assistant) )
Company: Integrated Resources, Inc ( IRI )
Posted on: June 23, 2022
Job Description Use Excel in partnership with Supply Chain
Execution Planners and Planner/Buyers to determine daily workload
requirements. Use Midas (document control system) to accurately
print required GMP documents. Accurately complete all required
documentation on GMP forms. Follow GMP ALCOA requirements for good
documentation practices: Accurate, Legible, Contemporaneous,
Original, and Attributable. Use SAP (ERP system) and Aera
(reporting tool) and MS Word to print non-GMP production cards.
Accurately compile all required forms into the batch record.
Maintain locked filing system for batch records. Issue batch
records to the shop floor adhering to lead times and standard work
to support production. Maintain schedule flexibility to support
production needs. May require off hours support. Complete all other
duties as assigned. Quals-- Required: Education- High school
diploma. Meticulous attention to detail, Motivated, Independent.
Prior System experience with SAP, Excel, Word. Heavily preferred:
former Client and/or Previous pharma experience, Midas or Qualidocs
(electronic document system) experience, Aera (reporting tool)
experience, attention to detail.
Keywords: Integrated Resources, Inc ( IRI ), Wilson , Document Control Administrator - I (Assistant) ), Other , Wilson, North Carolina
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