Baxter—Sr Eng, Codes and Standards

Job description

Description: This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride. Job Summary A Systems engineering professional with experience in product systems architecture and systems level design, product requirements management, Traceability, DHF structure & maintenance, Compliance management, plans, requirements & testing, Product Risk management, System level integration and Validation of medical devices. This position may own & perform relevant Systems activities for the PSS and GSS products. What you’ll be doing - Responsible for the coordination and development of the product systems architecture and systems level design, including the decomposition of the system architecture and requirements into subsystem and interface specifications. - Performs the activities associated with the Systems engineering of one or more products in various stages of the product lifecycle from new product development to post market surveillance. - Gathers inputs for Requirements from various sources such as Standards, User needs, Regulatory, Quality, Human factors, Manufacturing, Service and so on. Performs impacts assessment on the requirements on an ongoing basis for any proposed design/material/process change or an observation in the field/service or manufacturing to determine the impact and need for any mitigation. Come up with the recommended mitigation with the rationale. - Understands clinical and user need and can apply to product realization. Creates and maintains Design History File elements. - Leverages knowledge of technology, process, and/or therapy domains to drive solutions and product design realization from a systems perspective. - Drives adherence to FDA, ISO and IEC design control procedures, regulations and standards. - Can perform as an independent reviewer in technical and design reviews. - Interact with clinical and marketing to develop and refine user requirements. - Communicate design requirements and provide technical guidance to suppliers as needed. - Ensure user needs are captured, quality requirements are met and technical risks are mitigated. - Manage integration of deliverables from sub-system design teams and external partners. - Identify and define high level requirements for a product or a feature that enhance the quality of therapy - Identify and define high level requirements for a product or a feature that enhance the quality of therapy - Plan and execute system integration activities to minimize issues in systems validation. - Develop test plans, test protocols, and test reports for product integration testing. - Document traceability from requirements to verification activities, and from requirements to design entities. - Resolve systems-related technical issues by applying problem solving tools such as cause-and-effect diagrams, Pareto charts, etc. - Develop and maintain an effective and corroborative working relationship with internal and external development partners. - Develop System requirements; propose architectures and connectivity specifications of medical devices with each other and with external medical systems. - Ensure appropriate traceability between requirements, interface specifications, design and verification deliverables. As Compliance Engineer: - Coordination and management of standards compliance activities for assigned programs, working with cross-functional product development partners to identify requirements, developing and execute compliance plans, coordinate testing activities, reviewing compliance testing results and partner with certification agencies to certify products. - Partner with design engineers (Hardware, Mechanical, Software) to develop product requirements to comply with standards and regulations for intended use markets, develop Compliance Plans, participate in design and development activities and partner to resolve product certification, compliance and safety issues. - Consult with program teams on product certification strategy and compliance issues where needed - Facilitate and coordinate input from multiple cross-functional partners including Regulatory team, program management, R&D teams, manufacturing sites and service locations to develop comprehensive product certification and compliance strategies, and ensure that Baxter Healthcare solutions comply with product certification requirements in the intended use markets - Keep abreast of changes to product standards and regulations affecting medical products. - Ensure that all compliance test equipment complies with the test requirements specified in compliance standards. - Schedule compliance testing for Baxter Healthcare products at onsite test facility and at external test laboratories. Manage product test and certification projects with onsite and external test laboratories. - Prepare standards test reports and other documentation in accordance with applicable regulations. - Submit documentation to regulatory authorities as required to obtain product certifications for different global regions (e.g. US, Canada, Europe, Korea, Japan, Australia/New Zealand, Latin America, Caribbean, MEA) - Support the development System requirements and drive the cascade of the requirements to hardware and software subsystem requirements. - Ensure appropriate traceability between requirements, interface specifications, design and verification deliverables. - Identify compliance risks and reliability related requirements from applicable product standards (collateral and particular). - Collaborate with cross-functional resources (e.g. hardware, clinical, human factors, etc.) involved in designing for Compliance and ensure designs provide adequate margins. - Support sustaining teams in EMC investigation and identification of root causes. What you’ll bring - Must possess a strong knowledge of engineering disciplines and solid knowledge of related disciplines, Electromechanical, Systems, Fluid Mechanics, Materials Sciences - A demonstrated track record in electromechanical system development, preferably medical devices or other highly regulated products. - Strong team player, able to meet deadlines and handle changing priorities. - Experience in resolving complex technical problems using strong analytical skills. - Excellent written, oral and interpersonal skills - Must be proficient at time management and multitasking. As Compliance Engineer: - Knowledge of medical device requirements for Global (US, Canada, Europe, Korea, Japan, Australia/New Zealand, Latin America, Caribbean, MEA) - Knowledge and Hands on experience on all EMI/EMC standards/tests and knowledge of EMC regulations and certification procedures applicable to Medical Devices globally including testing documentation, certification requirements and procedures (i.e. IEC/EN60601, CISPR 11, FCC, EU, IC etc.). - Hands-on experience on Safety standards (IEC 60601 series) including collateral and particular standards - In depth knowledge on wireless regulations and standards (ETSI series, FCC, IC, RED (Radio equipment directives) for medical products - Familiarity with regulatory requirements of FDA and EU MDR. - Ability to perform diagnostics and correct EMC failures in conjunction with design engineers - Strong electronics background is essential - Strong experience in Requirements Management, Configuration Management, Defect Tracking and Traceability - Experience with EMC design tools, automated EMC testing tools, electronic test equipment (scopes, logic analyzers) - Knowledge of FDA's guidance on design controls and software validation, as well as ANSI/IEEE standards for EMC engineering - Demonstrated experience interfacing with regulatory agencies, conformity assessment bodies (UL, Intertek, CSA, etc.) and standards development organizations (IEC, ISO, NEMA, NFPA, ETSI, etc.). Education and/or Experience: - Graduate or Postgraduate in Biomedical, Mechanical, Electrical, Electronics or related Engineering. An advanced technical degree is desired. - 8-10 years of relevant technical experience in defining systems and requirements for medical products. Baxter is committed to supporting the need for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.