Manufacturing Coordinator

**City**:JUAREZ**State**:**Country**:Mexico**Business Area**:Production**Department**:Operations, Juárez**Employment Type**:Full-timeA global job position with an impactWe are seeking a highly organized, detail-oriented, and results-driven professional to join our manufacturing team as a Manufacturing Coordinator. In this role, you will be responsible for designing and maintaining production-related databases and dashboards, monitoring production performance, collecting and analyzing key operational data, supporting daily manufacturing operations, and ensuring alignment with quality and regulatory standards in a medical device manufacturing environment. You will play a critical role in supporting the decision-making process and driving data transparency across manufacturing operations.**Responsibilities and Essential Functions**:- Design, update, and maintain production databases with accurate, traceable, and regulatory-compliant data.- Develop and manage interactive dashboards to track key performance indicators (KPIs) such as throughput, yield, efficiency, downtime, and OEE.- Monitor daily and long-term production plans, proactively identifying variances and escalating potential risks to delivery or compliance.- Consolidate and analyze manufacturing data to support process optimization, root cause investigations, and continuous improvement initiatives.- Prepare daily, weekly, and monthly reports, presentations, and visual aids for production meetings and performance reviews.- Provide administrative and analytical support to the Manufacturing and Operations Management teams.- Ensure proper communication flow and data coordination between production, quality,planning, and engineering teams.- Support internal and external audit readiness by maintaining accurate documentation and data traceability aligned with QMS and ISO 13485 standards.- Recommend improvements to data collection systems and visualization tools to enhance decision-making and regulatory readiness.**Qualifications / Education**:- Bachelor's degree in industrial engineering, Manufacturing Engineering, Business Administration, Information Systems, or a related field.- Previous experience in data or administrative roles within a regulated manufacturing environment, preferably medical devices.- Knowledge of Good Manufacturing Practices (GMP), Quality Management Systems (QMS), and regulatory standards such as ISO 13485 and FDA 21 CFR Part 820.- Proficiency in database tools such as Microsoft Excel, Microsoft Access, or SQL for managing production and operational data.- Advanced user of data visualization platforms such as Power BI, Tableau, or similar tools.- Strong analytical and organizational skills with a proactive approach to problem-solving.- Ability to manage multiple priorities in a fast-paced, high-compliance environment.- Excellent communication skills, both written and verbal, with the ability to present technical data**Work Environment**:This is a manufacturing facility and as a result, employees have the potential to be exposed to noise, chemicals, fumes, airborne particles, machinery, vibration, or other workplace hazards controlled within compliance of current safety and health standards.**How to Apply**:About AmbuAmbu has been bringing the solutions of the future to life since 1937. Today, millions of patients and healthcare professionals worldwide depend on the efficiency, safety and performance of our single-use endoscopy, anaesthesia, and patient monitoring solutions. We continuously look to the future with a commitment to deliver innovative quality products that have a positive impact on patient care and the work of healthcare professionals. Headquartered near Copenhagen in Denmark, Ambu employs approximately 4,500 people in Europe, North America and the Asia Pacific.