Perform a varietyof day-to-day activities in support of the generation of Certificates ofAnalysis in support of release compounded sterile products. Tasks may includedata entry, file management and clerical work.
The QC Data Coordinator must payattention to details and have good organizational skills with large quantity ofdata. This position will work under the direction of the Quality ControlSupervisor.
1.Performs final check of routing forms containing potency,identification, sterility and endotoxins tests results.
2.Completes Certificate of Analysis for each batch.
3.Transfers the Quality Control documents to Quality Assurance department forfinal batch disposition.
4.Provides support to management in other data related tasks such asguardianship of matrixes and KPI.
5.Performs related duties as assigned.
1.1 year related experience in laboratory, quality or relatedexperience.
2.Ability to work independently, along with ability to work well within ateam, and willing to work overtime or off schedule as needed to meet demands ofCenter.
3.Must be highly organized and detail oriented
4.Ability to communicate effectively, both orally and in writing
5.Knowledge of GMP documentation, procedures, and systems as related.
6.Excellent computer skills (Microsoft Word and Excel)
1.High school diploma or GED required
Amerisourcebergen Corporation - Corporate