.Document Control CoordinatorApply locations: Mexico - TecateTime type: Full timePosted on: Posted 17 Days AgoJob requisition id: REQ40590Collaboration drives Nordson's success as a market leader in Industrial Precision Solutions and Advanced Technology. Our employees thrive in an environment where we help each other reach our personal best and enable our company to continuously improve and grow, and our customers to succeed. You will find Nordson employees sharing our success by giving back in the communities around the world where we live and work.ESSENTIAL DUTIES & RESPONSIBILITIES:Follow and work in accordance with Good Manufacturing Practices and Procedures as defined by Nordson Medical's policies and procedures, ensuring that FDA and Quality Standards are met.Maintain, update and archive primary and support documents in the company's document control system. Coordinate preparation, approval, and implementation.Review and process Change Orders (CO).Write and/or edit procedures, work instructions, or policies.Translate or coordinate the resources to translate documents as required.Ensure that documents provided to the manufacturing team are controlled and current.Review materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies, and ensure documentation is in English and Spanish.Distribute training to individuals and groups as required by training matrices.Create and manage training documentation files and follow up on overdue training.Assist in identifying training needs and work with all departments to provide effective training, as required.Administer Quality training for the site, including new hire training, periodic refresher training, and Quality Corners, as appropriate.Generate monthly metrics for incorporation into the Quality Monthly Report and to be posted as part of company metrics. Present data in update meetings.Provide additional data to management as required for Management Review and continuous improvement or failure investigation.Host or participate in internal or external quality audits; retrieve all requested controlled documents and manage any follow-up activities.Manage customer complaints, including communication with the customer, documenting all phases of the process, and tracking the complaint to completion.Lead the site's CAPA Review Board, including coordinating with CAPA owners, monitoring progress, and reporting results to management.Respond to internal and external controlled document requests; ensure accuracy of transmitted documents.Communicate effectively with all functions at the site, including with the Quality team.Exercise independent judgment in selecting and interpreting information and resolving difficulties.Maintain competency in all quality processes and procedures according to the training matrix.Maintain order and cleanliness of document control area and documentation files