Documentation Specialist
CurrentSt. Jude Medical is now Abbott Twenty two years of medical device experience working with regulated documentation, procedures, and quality systems. Extensive knowledge of PLM systems. Assure effective change order administration. Ensure that all change requests comply with procedure requirements. Maintain accurate configuration control. Control part numbers and revision level assignments. Maintain product configurations by ensuring accuracy of Bills of Materials. Monitor and prioritize routine documentation activities and requests to ensure customer expectations are met. Proofread documents for accuracy and adherence to policies, as necessary. Support Engineering projects to ensure accurate product configuration and documentation of products. Support project teams to ensure change requests are implemented to meet deadlines. Excellent time management skills and ability to work in a highly organized fashion. Work independently to resolve issues. Appropriately determine when to escalate to the next level of support. Effectively communicate and maintain a rapport with co-workers, technicians, engineers and managers. Experience in GMP, ISO and FDA controlled environments.