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Quality Control Senior Associate

West Greenwich, RI
Day to Day Responsibilities:
  • 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
Summary
  • 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"
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