12 Month ContractThe Compliance Specialist is responsible for all aspects of Documentation Management & Compliance.Responsibilities:Document Management• Manage the authoring & drafting of all types of Manufacturing Operations documentation.• Support document updates and manage timelines for cross functional Projects.• Act as a SME/Superuser on the Controlled Document System to facilitate the processing & approval of documents.• Organise & Facilitate Document Round Table meetings with cross functional teams.Compliance Tasks• Generate Reports/Metrics & analyze trends as required including but not limited to:Veeva QMS reports, Doc Tracker Lookaheads, ASI/AIC metrics, Logbook Metrics,Doc Tracker Metrics, RFT Metrics.• Perform Logbook Training, review, and trending of all closed logbooks.• Train and perform Area Self Inspections & Generate ASI schedule.• Train Manufacturing colleagues in GDP/GMP• Management of Veeva paper BindersRequirements:• 2+ years' experience in technical writing and compliance• Proficient in data analytics, data visualization• Working knowledge in Regulations, GMP, GDP• 2+ working within a regulated healthcare industry including a role in capacity of quality and compliance.