Sr. Documentation Control Specialist
Sequenom - San Diego, CA

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. The Sr. Documentation Control Specialist will be responsible for managing the Sequenom Center for Molecular Medicine (SCMM) documentation management, learning management, and record retention systems. The ideal candidate will maintain and oversee the document change control process including change orders affecting new product or process development; the training system; and storage of SCMM laboratory records. Additional responsibilities include implementing and configuring the electronic document management and electronic learning management system requirements, and supporting SCMM management during external audits from third parties (e.g. CAP, CLIA, State Accreditation Inspections). Responsibilities: Responsible for managing SCMM electronic Document Management System, electronic Learning Management system (MasterControl). Coordinate the interface with the business Enterprise Resource Management software (SAP) for new part BOM and router creation Develop and implement document control systems plans, polices, procedures and work instruction Manage and maintain all quality records and the document storage vault Manage revisions to document management system documentation, including Laboratory Operating Procedures and raw material/product specifications Provide support for development of training initiatives related to MasterControl and change control processes

The Ideal Candidate will have: Bachelor’s degree or equivalent combination of education and work related experience required. 8+ years of documentation control experience. Medical device, biotechnology ordiagnostic devices industry highly desired Prior direct experience with implementing, maintaining and improving a document control system Strong knowledge and skills with using MS office and Adobe applications including Outlook, Excel, and PowerPoint Experience with MasterControl and SAP strongly preferred Ability to handle multiple projects simultaneously

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