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Job • Develop and maintain system-level optical designs for components, subassemblies, and integrated flow cytometry platforms Perform Zemax (OpticStudio) modeling including performance prediction, tolerance analysis, sensitivity studies, and design trade-off evaluation • Define optical performance requirements and acceptance criteria at system and subsystem levels in collaboration with Systems Engineering • Define and execute optical integration, alignment, and calibration procedures to meet system-level performance requirements Analyze optical performance data to drive design optimization, improve system robustness, and reduce manufacturing and field variability • Support root cause investigations for system- and subsystem-level optical and laser alignment issues • Evaluate, test, and qualify optical components and modules, establishing acceptance criteria and improving incoming quality • Lead technical evaluation and qualification of optical suppliers (lasers, filters, lenses, fiber optics, detection modules) • Contribute across the full product lifecycle including concept, design, verification, and qualification in compliance with ISO 13485 and 21 CFR Part 820 • Collaborate with R&D, manufacturing, quality, and supply chain teams on design changes, NPI, and product transfers • Support development of next-generation optical architectures and platform strategies across flow cytometry systems • Provide support to Corrective and Preventative Actions (CAPA), End-of-life (EOL) component selection, and cost reduction activities. • Lead technical initiatives to resolve performance and supplier-related issues Travel domestically and internationally up to approximately 5% as required Education and • Experience Bachelor’s degree (minimum), Master’s degree (preferred), or PhD (desired) in Optics, Physics, or Optical/Mechanical/Electrical Engineering.

Job Summary We are seeking an exceptional and self-motivated Principal Algorithms Engineer to join our growing R&D team at Becton, Dickinson and Company located in Irvine, California.

Job • Reporting directly to the Associate Director of Quality, you'll be at the heart of our product development journey, applying your Quality Engineering expertise to both cutting-edge new products and essential product maintenance initiatives.

Possession of a valid Driver's License is mandatory, as the position will require travel between client sites, service locations, or field installations to perform necessary technical work.

Job • The Senior Process Engineer reports to the Senior Technical Leader. • Responsible for the implementation of project and process support activities toward attainment of departmental and plant goals.

Job Responsibilities • Be a Problem-Solving Detective • Design and conduct comprehensive Quality Engineering studies to identify root causes of quality non-conformances, then drive meaningful changes in processes, tooling, and product design to eliminate issues at their source Serve as the Technical Expert • Provide critical technical support to manufacturing teams and suppliers, helping resolve quality challenges • Lead Qualification Initiatives Perform thorough qualification studies for new suppliers, components, and cutting-edge inspection test equipment to maintain our high standards Master Validation Processes Plan and execute comprehensive validations (IQ/OQ/PQ) and qualification studies for new and existing equipment, including inspection systems, process equipment, software applications, and components • Create Quality Documentation • Develop clear, documented instructions for Quality Control inspections, including detailed Inspection Plans, Test Procedures, and Quality Standards that guide our teams Bridge Customer Requirements • Evaluate customer specifications and assess our capability to meet and exceed their expectations • Drive Continuous Improvement • Support broader manufacturing and business objectives by contributing innovative ideas, participating in implementation efforts, and serving on cross-functional committees, teams, and task forces • Manage Special Projects Take ownership of quality projects assigned by the Quality Engineering Manager, demonstrating your versatility and leadership • Ensure Product Conformance Exercise direct control over quality conformance for products in your assigned areas, maintaining our reputation for excellence Handle Material Reviews Complete Material Review Notices (MRNs), maintain accurate databases, and provide timely reporting to management on quality trends Review Critical Documentation Examine Device History Record (DHR) documentation for compliance and authorize release of components and finished products • Work in a Regulated Environment Thrive in our FDA cGMP, GDP, ISO 13485, and MDR-compliant medical device manufacturing facility where quality and compliance are paramount Required Qualifications Bachelor’s Degree in Engineering field 1 years QE Experience Experience in CAPA and root cause analysis Preferred Qualifications 3 years experience working in Quality Engineering Experience in validation and process controls FDA regulation experience Experience with ISO 13485 and 21CFR PART820 At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry.

Accountability • Support the maintaining of up-to-date knowledge and awareness of improvement methodologies and new techniques in maintenance engineering and their relevance to the site operations, including safety requirements, recommendations to ensure continuous improvements in equipment performance and availability as well as integration of maintenance best practices for BD equipment reliability for asset utilization. • Facilitate the definition of site maintenance strategies, procedures, and methods, aligning with maintenance budget and assets criticality.

Justification Addition Responsibilities may include but are not limited to • Ensure that all company safety rules and regulations are followed and promote general plant safety. • Work with Process Engineering to implement plant driven changes and provide overall support of process improvements by working with engineering teams to implement process improvements to improve Quality, conducting quality improvement projects through various CI initiatives. • Develop or update in-process inspection requirements to ensure the greatest value in process control for the customer and the plant during the manufacturing process while meeting regulatory requirements. • Provide assistance in such areas as process/equipment validation, process and product acceptance, audit correction actions, Change Control issuance for process changes. • Support CAPAs as owner or as part of the support team Monitor the performance of product lines for product quality metrics. • Work to implement document changes in support of ongoing efforts to simplify internal quality procedures in alignment with business unit and corporate requirements.

Job ESSENTIAL FUNCTIONS ( RESPONSIBILITIES • ) Essential functions include, but are not limited to, the following: • Manages and leads the Quality Systems and Quality Engineering activities for the designated BU. • Manages and support validation activities related to processes, products, materials and projects supporting the designated BU and other BUs when requested.

Job Experienced engineering resource to lead engineering projects in support of plant and company goals. Ensures compliance with BD quality systems, policies, procedures and best practices, and all local, state, federal and BD safety regulations, policies and procedures.

The Director, Quality Engineering will lead and strategically direct the quality engineering function, ensuring the design, development, and manufacturing of medical devices meet the highest standards of safety, efficacy, and regulatory compliance.

As part of the Systems Engineering group, the Systems Engineer II will play a key role in supporting the BD portfolio of products that involve electromechanical hemodynamic monitoring equipment.

This position is part of the Advanced Patient Monitoring (APM) business unit within BD's medical segment, aligning with BD's smart connected care approach As a Principal Systems Engineer, you will play a critical role in the design, development, and implementation of complex medical systems and devices.

Job • The Associate Director of Engineering is the senior engineering leader at the site level, responsible for engineering execution, technical governance, and performance.

Minimum Education Bachelor's degree required in Engineering, Mechanical Engineering preferred. Minimum Experience Two years medical manufacturing experience preferred.

Required Qualifications Bachelor's degree required in Engineering, Preferred Qualifications Bachelor's degree Mechanical Engineering Two years medical manufacturing experience Three years manufacturing experience High speed, automated manufacturing experience At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry.

Required Qualifications Bachelor's degree in Engineering Preferred Qualifications Bachelor's degree in Mechanical Engineering Two years medical manufacturing experience Three years manufacturing experience At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry.

Responsibilities • Lead cross-functional teams to successfully launch new medical device products in global markets, ensuring alignment across engineering, manufacturing, quality, and commercial functions. • Drive product design and development using concurrent engineering principles, ensuring alignment with design objectives and customer/user needs.

Job • The Staff Quality Engineer is a key member of the New Products Development Team and is responsible for • Design Control activities from research through product launch.

Job Summary • We are seeking a highly experienced Senior Staff Algorithm Engineer with deep expertise in physiological signal processing, biomedical sensor data, and classical machine learning to help develop next-generation medical technologies for continuous patient monitoring, disease detection, and predictive clinical insights.