Position Summary: Provides technical support for product quality, continuous improvement, and process reliability by analyzing metrics and recommending adjustments. Key Highlights: 1. Support quality and continuous improvement of disposable products and processes. 2. Analyze quality metrics and recommend design and manufacturing adjustments. 3. Participate in the analysis of medical product and process proposals. **Job ID** R\-535772 **Date posted** 06 March 2026 **Job Description Summary** =========================== Provide technical support for processes, quality of disposable products, and effectiveness in continuously improving material, product, or quality and process reliability. Generate and analyze quality metrics and recommend adjustments to product design, manufacturing processes, and quality systems.**Job Description** =================== * Participate, as applicable, in analyzing product and process proposals compliant with regulations for medical device manufacturing. * Responsible for analyzing in-process quality data and recommending adjustments to product design, manufacturing processes, equipment, and quality systems as required. * Maintain updated performance metrics for their area. * Participate in the review and disposition of nonconforming material during Material Review Board (MRB) meetings, evaluating risk and impact, engineering change orders; additionally, follow up on corrective and preventive actions. * Participate in product complaint evaluation and provide corrective actions. * Review and update inspection and test method documents; additionally, may update manufacturing process documentation, layouts, etc. * Provide product and process training to quality personnel when required. * Validate and implement test equipment, as well as participate in the design and validation of test fixtures; participate in Kaizen and other continuous improvement activities. * Track and ensure timely and proper implementation of CAPA, QNs, Q7s systems, audit execution and results. * Participate in equipment, process, and product validation and transfer; also participate in cost reduction projects and support environmental incident response actions within assigned areas. * Collaborate in failure investigations during validation processes for new components and processes. **Requirements:** * 2–3 years in similar positions. * University degree (mandatory) in Industrial Engineering or related field. * Conversational English (Advanced). * Experience in the medical device industry (preferred). * Proficiency in industrial process management and control. * High level of leadership and development. ### **"BD values equity in the workplace and does not discriminate against any disability, class, ethnicity, age, religion, gender identity, or sexual orientation."** Required Skills Optional Skills . **Primary Work Location** ========================= MEX Tijuana \- Alaris El Florido**Additional Locations** ======================== **Work Shift** ==============