8 Qfd Jobs

The role of Senior Engineer Systems& MBD is to contribute to design and development of a product or solution, from conception to design and verification/validation. You will apply expert technical knowledge and engineering principles in the development of products and solutions. You will help accelerate the design and development cycle by employing model based design principles and developing MATLAB models working together with the hardware and software teams. You will collaborate with cross functional team for technical issues, design changes, design reviews, and complex problem resolution. This position is based out of Bangalore and reporting to the Manager Systems and V&V for Patient Support Systems and Global Surgical Solutions divisions. Essential Duties and Responsibilities : Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, Design trade-offs and Risk assessment early in the development cycle working independently or under the guidance of senior staff. Use MATLAB to develop Model Based Design working together with hardware and software teams and help accelerate product development cycle. Provide your technical expertise to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle. Excels in the development of Use Case for product or solution based on intimate knowledge of customers and their environments. Use industry standard tools and excel spreadsheets in the management of requirements and decomposition of system level requirements to modules. Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety. Identify development issues and facilitates in the resolution using optimal technology solutions. Supports in the Usability Engineering activities to ensure the application of human factor in the development of products or solutions to demonstrate compliance to IEC 62366 and FDA guidance. Knowledge in the application of principles of Reliability and Robustness in the development of products or solution. Completes detailed, high quality technical documentation to capture and communicate designs. Support integration issues during development tests and ensure module / system development is successful. Actively collaborate with software and hardware engineers to aid in the design development. Actively engage with verification and validation engineers to aid in the development of verification test plans with good test coverage. Your Team: This position will be reporting to the Manager Systems and V&V for Patient Support Systems and Global Surgical Solutions divisions. This position does not have any direct reports. You will need to work collaboratively with R&D and cross functions. Your Location: The role is in Baxter R&D facility in Bangalore India. What You'll Bring: Bachelor's Degree with 6+ years or Masters with 3+years experience in Bio-medical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Mechanical Engineering, Industrial Engineering or related field Experience in System engineering function of Medical device/ Medical Imaging / Image processing, with hands on experience developing MATLAB system models. Experience in Medical Device development, FDA Regulations and MDR. Exposure to Usability Engineering Process Experience in QFD, Pugh Matrix, CTQ, DFR, DFX Strong interpersonal skills with the ability to collaborate with others in a team environment

For us, working at Baxter is not just a jobit's a calling. Our mission to save and sustain lives unites us. We are driven not by what will be easy, but what will transform global healthcare for generations to come. Together, we create a place where we are happy, successful and inspire each other as we pursue rewarding careers. We're grateful you're interested in continuing your career journey with Baxter. This is where your purpose accelerates our mission and make a positive impact on millions of people around the world. JOB SUMMARY: A Systems engineering professional with experience in Systems areas like Product Requirements, management, Traceability, DHF structure & maintenance, Product Risk management, System integration, and Verification & Validation of medical devices. This position own & perform relevant Systems activities for a family of products for both PSS & GSS. The role of Principal Engineer Systems& MBD is to contribute in design and development of a product or solution, from conception to design and verification/validation. You will apply expert technical knowledge and engineering principles in the development of products and solutions. You will help accelerate the design and development cycle by employing model based design principles and developing MATLAB models working together with the hardware and software teams. You will collaborate with cross functional team for technical issues, design changes, design reviews, and complex problem resolution. This position is based out of Bangalore and reporting to the Manager Systems, Patient Support Systems and Global Surgical Solutions divisions. Essential Duties and Responsibilities : Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, Design trade-offs and Risk assessment early in the development cycle working independently or under the guidance of senior staff. Use MATLAB to develop Model Based Design working together with hardware and software teams and help accelerate product development cycle. Provide your technical expertise to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle. Excels in the development of Use Case for product or solution based on intimate knowledge of customers and their environments. Use industry standard tools and excel spreadsheets in the management of requirements and decomposition of system level requirements to modules. Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety. Identify development issues and facilitates in the resolution using optimal technology solutions. Supports in the Usability Engineering activities to ensure the application of human factor in the development of products or solutions to demonstrate compliance to IEC 62366 and FDA guidance. Knowledge in the application of principles of Reliability and Robustness in the development of products or solution. Completes detailed, high quality technical documentation to capture and communicate designs. Support integration issues during development tests and ensure module / system development is successful. Actively collaborate with software and hardware engineers to aid in the design development. Actively engage with verification and validation engineers to aid in the development of verification test plans with good test coverage. Involved from new product development to post market surveillance at various stages of product lifecycle. Primary point of contact for R&D for PMO & cross-functional team for integration, execution, project deliverables, budget & resource needs. Your Team: This position will be reporting to the Manager Systems, Patient Support Systems and Global Surgical Solutions divisions. This position does not have any direct reports. You will need to work collaboratively with R&D and cross functions. Your Location: The role is in Baxter R&D facility in Bangalore India. What You'll Bring: Bachelor's Degree with 12+ years or Masters with 8+years experience in Bio-medical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Mechanical Engineering, Industrial Engineering or related field Experience in System engineering function of Medical device/ Medical Imaging / Image processing, with hands on experience developing MATLAB system models. Experience in Medical Device development, FDA Regulations and MDR. Exposure to Usability Engineering Process Experience in QFD, Pugh Matrix, CTQ, DFR, DFX Strong interpersonal skills with the ability to collaborate with others in a team environment Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards. Demonstrated experience in accomplishing objectives. Able to deliver on multiple projects simultaneously Self-motivated with good interpersonal skills Able to deliver on multiple projects simultaneously Ability to identify compliance risks and escalate, when necessary, Excellent verbal and written English communication skills, suitable for multi-location working relationships, Demonstrated teamwork and collaboration skills, Aptitude for Mindfulness and attention to detail,

Job Description The role of Engineer II, Systems is to contribute in design and development of a product or solution, from conception to design and verification/validation. You will apply expert technical knowledge and engineering principles in the development of products and solutions. You will help accelerate the design and development cycle by employing model based design principles and developing MATLAB models working together with the hardware and software teams. You will collaborate with cross functional team for technical issues, design changes, design reviews, and complex problem resolution. This position is based out of Bangalore and reporting to the Manager Systems Engineering for Patient Support Systems and Global Surgical Solutions divisions. Essential Duties and Responsibilities : Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, Design trade-offs and Risk assessment early in the development cycle working independently or under the guidance of senior staff. Use MATLAB to develop Model Based Design working together with hardware and software teams, and help accelerate product development cycle. Provide your technical expertise to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle. Excels in the development of Use Case for product or solution based on intimate knowledge of customers and their environments. Use industry standard tools and excel spreadsheets in the management of requirements and decomposition of system level requirements to modules. Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety. Identify development issues and facilitates in the resolution using optimal technology solutions. Supports in the Usability Engineering activities to ensure the application of human factor in the development of products or solutions to demonstrate compliance to IEC 62366 and FDA guidance. Knowledge in the application of principles of Reliability and Robustness in the development of products or solution. Completes detailed, high quality technical documentation to capture and communicate designs. Support integration issues during development tests and ensure module / system development is successful. Actively collaborate with software and hardware engineers to aid in the design development. Actively engage with verification and validation engineers to aid in the development of verification test plans with good test coverage. Your Team: This position will be reporting to the Manager Systems Engineering for Patient Support Systems and Global Surgical Solutions divisions. This position does not have any direct reports. You will need to work collaboratively with R&D and cross functions. Your Location: The role is in Baxter R&D facility in Bangalore India. What You'll Bring: Bachelor's Degree with 6+ years or Masters with 3+years experience in Bio-medical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Mechanical Engineering, Industrial Engineering or related field Experience in System engineering function of Medical device/ Medical Imaging / Image processing, with hands on experience developing MATLAB system models. Experience in Medical Device development, FDA Regulations and MDR. Exposure to Usability Engineering Process Experience in QFD, Pugh Matrix, CTQ, DFR, DFX Strong interpersonal skills with the ability to collaborate with others in a team environment Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards. Demonstrated experience in accomplishing objectives. Able to deliver on multiple projects simultaneously Self-motivated with good interpersonal skills

MANAGER PMO AND SERVICE DELIVERY - OculusIT MANAGER PMO AND SERVICE DELIVERY MANAGER PMO AND SERVICE DELIVERY Position MANAGER PMO AND SERVICE DELIVERY Location Gurgaon Reporting Manager Program Manager Shift Timings 8:00 AM-5:00 PM (EST) Key Responsibilities: Build strategic roadmaps and drive achievement of key milestones for our largest and critical customers in a post-sales relationship. Engage with Director and C-Level executives to understand business needs and establish strong executive relationships. Be involved in the change management process of the customers environment to ensure success and service uptime Go toe to toe with customer technical stakeholders on most issues, and use your judgment when to pull in the heavyweight engineers / consultants / architects as necessary. Establish working relationships with other AISPL account team members such as AMs, BDMs to achieve best results for the customer. Be available outside of business hours to help coordinate the handling of urgent issues as needed. Ensure achievement of the SLA metrics, service KPI s and customer satisfaction. Person should have a strong understanding of projects lifecycle and deliverables of each phase. Should be good in agile development methodology Knowledge of six sigma and its tools that helps in different phases of project e. g. QFD, FMEA, Fish-Bone etc. The candidate should have led large size programs and have a proven delivery track record as a project manager. Should be able to handle multiple priorities in parallel. Required Experience: 8 11 years of experience Desired Qualification: A professional certification in any or all of the following: Relevant Bachelor s degree/ Preferred Graduate / Masters in Computers / IT or equivalent academic qualification. PMP Certification. ITIL Certification. Desired Skills: Strong team player The role entails working with multiple The VP Service Delivery & PMO will focus on the transition period or defined transformation period and ensure the orderly, utilizing established Transition methodologies, activities and work product, helping clients to achieve a higher level of maturity by directing, facilitating, coordinating, tracking and reporting on the successful execution and completion of projects. Should develop project plans for the transformation, educate the Transformation Team on the appropriate Transformation Methodology, deploy consistent project management techniques, and lead process improvement projects and activities. Should be able to lead a team of Project / Transition managers and Application Support engineers teams hence the candidate would need to display inclusiveness to lead as well as take the team along the life of the Program. Collaborates well with others to solve problems and actively incorporates input from various sources. Strong analytical skills strong problem-solving skills, communicates in a clear and succinct manner and effectively evaluates information / data to make decisions; anticipates obstacles and develops plans to resolve Demonstrated customer focus. Person needs to effectively manage business and IT stakeholders through regular reviews and effective communication. He should also be a strong team player ensuring great collaboration inter and intra teams for effective execution. Should demonstrate proven senior stakeholder management experience, Clear leadership and communication skills. Joe Redwine Joe brings almost 25 years of experience building innovative higher education technology services companies. He is a retired USAF officer providing leadership in the areas of space, intelligence, and flight operations. Joe is a collaborative leader known for his passion for building teams focused on customer needs. He previously served as VP of Client Experience at CampusWorks and COO of Dynamic Campus.

Job Role & Responsibility: Internal audit Planning and monitoring Audit as per the apex Procedures & QMS for the different departments of the organization Analyze and evaluate audit data. Prepare and present reports that reflect audit s results. Identify weak areas related to QMS Build robust systems based on best practices being followed in the industry to improve adherence. Improvement of weak areas and re-audit for confirmation Thorough understanding & grasp of basic Quality Management Tools like PFMEA, 7 QC Tools, 5 Why, QFD, Six Sigma, SPC, MSA etc. Organize & Conduct training sessions on QMS Regularly compile best practices related to QMS being followed at various OEMs Competency Requirement:- Technical/Functional: Knowledge of Quality Management Systems. Proven knowledge of auditing standards and procedures and regulations Knowledge on automobile products/ processes Lead assessor course or Internal auditor course for ISO 9001 and IATF- 16949. Knowledge of Quality Management Tools & Statistical techniques like SPC/ MSA/ FMEA/ PPAP/ APQP. Awareness about the latest updates on best-in-class industry practices skill. Behavioral: Auditing and observation / listening skills. Communication and teamwork Analytical skills Presentation skills & IT Skills Coordination / Networking skills Others: Bachelor s degree in Automobile/Mechanical Engineering Years of experience: Should have 8-12 yrs. Exposure of (4-wheeler / 2-Wheeler) & Automotive products Basic knowledge of manufacturing processes like welding / press / machining casting / molding / Heat treatment/ Assy / Inspection Worked as an internal auditor / certified lead auditor for QMS Knowledge of Vehicle Regulations i.e. India (AIS / IS Standards) & Export (ECE) Implementation & audit of ISO 9001:2015

Research and Development - Setco Auto Systems Highly Qualified Our Research Development Center with our highly qualified and experienced team are our backbone that provides the competitive strength and edge. Our focus on quality, cost, testing, design technology of our premier products ensures that we bring the best to the customer stables in a timely manner. Research and Development Hub Our state of the art research and development center at Kalol, certified by the Department of Scientific Industrial Research (DSIR), Government of India to design, develop and validate full clutch systems. The center has a well equipped RD Office in the UK as well. Global RD Expertise Our RD facilities in India and UK play a key role in meeting our customers exacting demands by geography and operating cycles. Advanced RD Capabilities Key capabilities at our RD facilities include cutting-edge software and tools in drafting, 3D modeling, product lifecycle management, project management, clutch testing and analysis, sample development and ensure that our place in cemented in the minds of our customers. Innovative and Versatile Design Development SETCOs Design Development team, built with top-tier talent, excels in creating products from the initial concept stage to final vehicle installation. With the ability to design components from 159 mm to 430 mm, SETCO meets a wide range of torque and RPM requirements. The team also pioneers alternative materials, ensuring the products are widely used in both domestic and export markets. Comprehensive Expertise and Tailored Solutions The range of expertise available covers a vast segment Mechanical, Chemical, Computer, Hydraulic, Pneumatic, Manufacturing, Assembly Automation, Logistics, etc. SETCO also undertakes reverse engineering to suit specific customer needs and designs test rigs to meet customer validation programs. Confidential Collaboration and Customer-Centric Solutions SETCO maintains absolute confidentiality in their interactions with customers and offers suggestions on vehicle installations not only for the betterment of the products but also for the customers. SETCO deploys the following tools and techniques during its various stages of product design and development Design for Assembly (DFA) Design for Manufacturing (DFM) Design for Six Sigma (DFSS) Design for VAVE Design FMEA (Failure Mode and Effect Analysis) Design for Service and Recyclability Design of Experiments (DOE) Quality Function Deployment (QFD) Testing is an integral part of product development, qualification, and evaluation of system performance. Even though computer simulation helps to eliminate some interaction steps, final practical steps remain a necessity and these are achieved through simulated test rigs. The product validation is either as per LIPE test conditions or as per customer-specific test conditions. The test engineers are experienced with defining test parameters, performing tests, processing test results, and making statistical evaluations. SETCO has designed various test rigs for testing the ultimate product, and a few of the test rigs used for various parameters are listed below:

Provide leadership for quality activities associated with NPD & quality system tools/ procedures to support NPD Processes.Set new product quality metrics for organization, provide performance feedback & lead corrective action activities as needed. Required Candidate profile Track product lifecycle quality performance & identify design improvement 4 quality improvement 2 deliver.Define corporate quality system improvement strategies 4 NPD Processes & drive implementation

Internal audit Planning and monitoring Audit as per the apex Procedures QMS for the different departments of the organization Analyze and evaluate audit data. Prepare and present reports that reflect audit s results. Identify weak areas related to QMS Build robust systems based on best practices being followed in the industry to improve adherence. Improvement of weak areas and re-audit for confirmation Thorough understanding grasp of basic Quality Management Tools like PFMEA, 7 QC Tools, 5 Why, QFD, Six Sigma, SPC, MSA etc. Organize Conduct training sessions on QMS Regularly compile best practices related to QMS being followed at various OEMs a. Technical/Functional: Knowledge of Quality Management Systems. Proven knowledge of auditing standards and procedures and regulations Knowledge on automobile products/ processes Certified internal auditor course for ISO 9001 and IATF- 16949. Knowledge of Quality Management Tools Statistical techniques like SPC/ MSA/ FMEA/ PPAP/ APQP. Awareness about the latest updates on best-in-class industry practices