Location:
Boston, MA – Hybrid (3 days/week onsite)
Start Date:
ASAP
Duration:
6-8 months plus
Description:
The client has transition last year from paper base to master control. The client needs a consultant who comes from a quality GMP background who is self sufficient can support a given workflow and know how to retrieve and revise SOPs, open deviations, provide corrections and then close out deviations and initiating CAPAs.
Need someone to be able to work independently who can work directly with master control services.
Generating reports with all the data that will be able to smoothly configure reports.
Understands usability of workflows
Skills:
Document Control, workflow understanding, eQMS administration of document control
Doc Control Specialist (232515) Hybrid – MA
