Quality Engineer

Description

Job Summary: Provides technical support for the process and quality of disposable products, continuously improving materials, products, and process reliability, as well as analyzing quality metrics and recommending adjustments. Key Highlights: 1. Participates in the analysis and improvement of medical products and processes. 2. Leads the evaluation and adjustment of product designs and manufacturing processes. 3. Collaborates in failure investigations and cost-reduction projects. **Job ID** R\-535772 **Date posted** 06 March 2026 **Job Description Summary** =========================== Provide technical support to the process and quality of disposable products, effectively driving continuous improvement of materials, products, process quality, and reliability. Generate and analyze quality metrics and recommend adjustments to product design, manufacturing processes, and quality systems.**Job Description** =================== * Participates, 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. * Maintains up-to-date performance metrics for their area. * Participates in the review and disposition of nonconforming material at the Material Review Board (MRB), evaluating risk and impact, engineering change orders; additionally, follows up on corrective and preventive actions. * Participates in product complaint evaluations and provides corrective actions. * Reviews and updates inspection and test method documentation; may also update manufacturing process documentation, layouts, etc. * Provides product- and process-related training to quality personnel when required. * Validates and implements test equipment, as well as participates in the design and validation of test fixtures; engages in Kaizen and other continuous improvement activities. * Tracks and ensures timely and proper implementation of CAPA, QNs, Q7s systems, and audit execution and results. * Participates in equipment, process, and product validation and transfer; also participates in cost-reduction projects and supports environmental incident response actions within assigned areas. * Collaborates in failure investigations during validation processes for new components and processes. **Requirements:** * 2–3 years in similar positions. * Bachelor’s degree (mandatory) in Industrial Engineering or related field. * Advanced conversational English. * Experience in the medical device industry (preferred). * Proficiency in industrial process management and control. * Strong leadership and development capabilities. ### **"BD values workplace equity 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** ==============