Working with lab staff and management to author/revise GMP records, creating a tracker to monitor ongoing project activities, follow up with lab staff for deliverables, setting up and leading meetings as needed.
Additional support may involve working with lab staff on non-test laboratory tasks to assist keeping the lab efficient and compliant
Ideal candidate- Must have GMP experience, GMP technical writing skills, Project management skills, and lab exp. a plus.
Experience with owning an updating GMP related documents GMP records.
Under general supervision this position will primarily provide administrative support to the Raw Material Centralized testing laboratory, including but not limited to:
Authoring/revising GMP records to document verification work done in the lab, compiling and managing a tracker to coordinate specific lab project work, monitoring various work-streams in the laboratory.
Secondary work may include assisting directly in the laboratory around sample management, disposal and good documentation compliance reviews.
Must learn and comply with safety guidelines, GLP, and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory notebooks, written procedures, building monitoring systems and laboratory log books.;
Skills: lab experience "This posting is for Contingent Worker, not an FTE"