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This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives.
Understanding of business, market, industry and competitive knowledge & integrating into technical solutions that can be readily adapted to changes in technology and/or clinical use
Generates alternatives and takes reasonable risks while solving technical problems
Work and collaborate closely with Project Manager & Team leads to define and solve engineering changes/problems to make products that meet all performance and functional criteria within required project schedule, with minimum guidance
Participate in design/change reviews with the Sustaining Team and Engineering Change Board – justify design detail and collaborate with other team members
Completes detailed, high quality technical documentation of product designs through the generation and maintenance of design requirement specifications, engineering prints, material specifications and bills-of-materials
Uses existing engineering tools and best practices to report and track product and process metrics
Challenges project teams and established work processes and proactively finds creative methods to reach desired performance levels
Informs others proactively about developments or issues that affect their work, and their ability to meet commitments
Presents the findings / objective evidences and able to present with rationale with applicability / exclusions
Identify and report any quality or compliance concerns and take immediate corrective / Preventive action as needed
Requirements
Experience in Requirement analysis, flow down, risk assessment, system thinking
Develop or refine user/product requirements and work with developers for their implementation and testing
Involvement in the system and medical risk management activities for our products and ensuring the safety of the product for patients and caregivers
Resolve systems-related technical issues by applying problem-solving tools such as cause and effect diagrams, 5 Whys, Pareto charts, etc.
Experience in electromechanical hardware development, preferably medical devices or other highly regulated products such as military hardware
Ability to generate alternative solutions to problems or processes
Simulate therapy algorithms using modeling & simulation software like Matlab/Simulink. Ability to apply engineering concepts to electro-mechanical systems with software, their functionality, connectivity, and usability aspects
Strong interpersonal skills with the ability to work collaboratively with others in a team environment
Excellent background in fundamentals of circuit design and analysis
Experience with industry leading software tools for schematic entry and PCB layout design
Experience with established development tools and processes. Especially Altium, PSpice, OrCAD, Mentor's DxDesigner and Expedition
Hands-on experience with analog/digital circuit and embedded systems designs is required
Hands-on experience with embedded platforms, 8-, 16- and 32-bit microcontrollers, Arm Cortex-M series processors
Experience in CAN, SPI, I2C and UART
Experience in designing circuits involving more than one of the following is preferred: Battery, Blower, Compressor, Motor control and Solenoid control
Previous exposure with Medical Devices, FDA Regulations or other applicable regulatory requirements
Working knowledge of UL/IEC 60601-1, ISO13485 and CE/UL certification is a plus
Working knowledge in design QA, DFx, and DFMEA are preferred
Demonstrated experience in accomplishing objectives. Able to deliver on multiple projects simultaneously
Self-motivated with good interpersonal skills
Bachelor's Degree in Electrical/ Electronic engineering with 7-11 yrs. of work experience in Systems Engineering, Design and Development, testing of complex electrical/ Electronic components/ subsystems/ systems & products
Nice to have
Working knowledge of UL/IEC 60601-1, ISO13485 and CE/UL certification is a plus
Working knowledge in design QA, DFx, and DFMEA are preferred