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**Job Description Summary**: The Documentation Engineer participates in all aspects of the Electronic Documentation System.Participates and assists in creating documents according to established standards.Assists in the fulfillment of departmental and plants goals. Develops his/her skills to train and lead.Participates in Lean Thinking activities/events.For more than 125 years, we’ve pursued our Purpose of advancing the world of health. We relentlessly commit to a promising future by developing innovative technologies, services and solutions, helping the healthcare community improve safety and increase efficiency. It takes the imagination and passion of all of us at BD, from the manufacturing to marketing of our products, to look at the impossible and find transformative solutions to turn dreams into possibilities - For people today, tomorrow and beyond. Become a maker of possible with usDevelops Documentation Engineering functions:Processes and reviews CR Packets.Reviews change requests for administrative routes.Ensures the release of project documents in the MasterControl System.Designates MFG and Waiver numbers.Gives Quality System technical advice to other departments.Controls Project data inputs.Manages approval panels.Makes DMR and BMD Document Control numbers.Consults obsolete documents in MasterControl and Legacy.Assists in the training of employees from the Document Control department and new Power Users fromother departments.Participates in the design, development and implementation of documentation systems and projectsmanagement.Assists in the fulfillment of departmental and plants goals that help with the continuous improvementand supporting of divisional and corporate goals.Participates in the implementation of quality programs that promote an environment of prevention andno detection of defects or problems.Participates with the personnel of other disciplines (Engineering, Production, Quality, etc.) in thedevelopment of documents and completion of activities of different plant projects.Participates as an internal auditor in the verification of the quality system to meet with ISO 13485:2016of the Quality System Regulation (QSR)/Good Manufacturing Practices (GMP’s) as well as regulationsand internal policies, divisional, corporate, and regulatory organizations.Proposes changes for the continuous improvement of processes, products, processes, and methods.Participates in the elaboration and/or revision of documents in general.Represents the department of Quality Assurance in meetings of projects or other departments.Participates in planning meeting, implementation, following or evaluation of goal s, or departmentprojects.Participates in the implementation of Lean Manufacturing/Lean Thinking tools.Works directly with translators in assigning tasks and coordination of changes.Develops Visual System Maps (VSM) and proposes improvements.Any other task assigned by his/her immediate boss.Education and Experience:High School or Technical Career preferably completed.No experience needed.To be studying a professional career in any branch of Engineering or preferably, to be a recent graduateintern.Knowledge and Skills:Provides ideas for continuous improvement.LeadershipEffective Communication.Able to self-train.To learn computerized and electronic systems with ease.Mathematical skills of Bachelor’s degree.English level: Upper Intermediate“BD values equity in the workplace without discrimination for any disability, class, ethnicity, age, religion, gender identity or sexual orientation.”**Primary Work Location**: MEX Nogales South - Parque Industrial El Cid**Additional Locations**:**Work Shift**:
