Technical Writer with 8 years experience in the Pharmaceutical Industry to support the assessment, improvement, standardization and/or creation of manufacturing and packaging procedures and production documentation across multiple sites. Knowledge of current Good Manufacturing Practices and Regulatory guidelines for Pharmaceutical Industry.
This is a 12- 24 month assignment.
Manufacturing and Packaging processes, procedures and documentation (Material Weighing thru Finished Product to Warehouse)
Incorporate cGMP, Quality & Compliance standards into all phases of Operations where required
Standard Operating Procedure, Batch Record & production process documentation creation/improvement through approval
Multiple site engagement and collaboration – Philadelphia Metro Area and Puerto Rico (Home Office & Plant)
