83908
- Please ONLY local candidates to Bothell WA
- MUST have pharmaceutical exp
- 100% Onsite - Work Schedule- Sun- Tues OR Tues - Sat- 8am-5pm!
TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.
Our client, a leading pharmaceutical company is hiring a QA Associate Specialist Document Control for a 12+ months contracting assignment.
Must have skills :
Minimum of 3+ years of relevant document control records management experience in a cGMP / FDA regulated environmentExperience with an Electronic management systemDemonstrated experience with quality management systemsDemonstrated knowledge of at least one enterprise computer-related system used for recording of Quality System data (e.g., Content Manager Records Software)Bachelors degree or equivalent - Library Science a plusExperience in FDA / EMA regulations in biopharmaceuticals or cell therapy manufacturing is requiredExperience with Part 11 adherence regarding scanning of records and electronic archivingStrong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System)Strong knowledge of cGMPs and domestic regulatory requirementsKnowledge of Records Management, Scanning and organization functionsPay : $42-$44 / hour W2
Location : Bothell WA
Responsibilities :
Receiving and reconciliation of GMP records, management of scanning, archival and retention of GMP recordsResponsible for the organization of cGXP controlled document files within the DocumentCenter and ensure that records are readily retrievable and sent off to final archive facility as neededAssist with Document Center Archive room activitiesFollow Policies, SOPs, and work instructions to support the document approval process, assign effective dates and training workflows, and archive documents and document change requestsExecute the process and procedures for identifying, collecting, distributing and filing the controlled documents for the siteSupport internal and external audits and regulatory inspectionsAssist with document retrieval / organization support during regulatory inspectionsAssist with Insurance and Reconciliation of Controlled Forms and Logbooks