Overview In this Quality Systems Consultant role at a small biotech near Boston, you will support GxP document management and training programs. You will own hands-on administration of critical systems like ZenQMS and Box GxP, helping maintain data integrity and compliant quality processes. You'll work with cross-functional teams to implement and train on standard documents, SOPs, and training materials. This is a three-month engagement with potential extension, offering impactful work shaping quality systems in a biotech environment. ResponsibilitiesSupport document management activities (policies, SOPs, specifications) and training administrationAdminister ZenQMS and Box GxP for daily useManage eDMS/eQMS administration and training activitiesPrepare SOPs, work practices, and user guides for quality system requirementsDeliver and develop quality system training presentations; communicate performance metrics to management Key requirementsBS degree in Life Sciences or related fieldMinimum 4 years in pharmaceutical QA and GxP regulatory complianceHands-on experience with eDMS/eQMS, eLMS; administering Box GxP and ZenQMSWorking knowledge of US/EU GxP related to document management, training, data integrity, and quality systemsStrong oral and written communication; ability to train system users; ability to create user guidesstrong communicationpresentation skillstraining deliveryZenQMS administrationBox GxP administrationeDMS/eQMS administration
Not specified in the original listing.
Not specified in the original listing.
