Description/Duties:
Position will be responsible for Scheduling of the Commissioning, Qualification, and Validation including documentation of a Pharmaceutical Manufacturing facility.
This assignment is for the ?back end? of the project.
Using P6, to plan and schedule the start-up commissioning and validation efforts to bring the new process into production.
Coordinate schedule with schedules from CM, Start-up, Validation teams and plant operations.
Requirements:
Must have 10+ years experience.
Must have experience in Primavera P6.
Must have prior/recent Pharmaceutical/Biopharmaceutical GMP experience.
Must have Qualification, and Validation scheduling experience.
Local candidates preferred, but there is a per diem available for the right candidate.