- Baxter International Inc. is an American multinational healthcare company with headquarters in Deerfield, Illinois. The company primarily focuses on products to treat kidney disease, and other chronic and acute medical conditions.
Baxter is hiring for Mechanical Engineer
The job you are looking for is no longer available..- Company Name
- Baxter
- Company Website
- https://www.baxter.com/
- Experience
- 12+ years
- Job Role
- Principal Engineer
- Job Type
-
- Experienced
- Job Location
-
- Bengaluru/Bangalore
- Education
-
- BE/BTech
- Branch
-
- Mechanical Engineering
- Job will expire on
- 17 May 2024
About Company
Eligibility Criteria
- Bachelor’s Degree in Mechanical engineering with 12+ years of experience, or master’s in mechanical engineering with 9+ years of experience.
- Demonstrated experience in end to end product development from concept to manufacturing transfer, preferably those involving structural design, mechanism design, precision positioning, and electronics packaging.
- Medical device, diagnostics, laboratory testing product or similar products design & development experience is preferred.
- Must be well versed in engineering disciplines (e.g. Mechanical systems, Materials, Plastics, Mechanism design, Metal fabrication, Welding, Fluid management, Pumps/ Blowers, Integration of motors, Actuators & Sensors, Simulation)
Job Description
- Be the subject matter expert in Mechanical Engineering and design, development and manufacturing transfer of PSS & GSS products
- Ability to lead by example, ensuring clear accountability and operational excellence. Ensure effective performance management.
- Collaborate across multiple locations & functional teams such as Electrical hardware Systems Engineering, Verification & Validation, Advanced manufacturing teams, as well as manufacturing partners / suppliers to ensure the projects are executed effectively, to budget & schedule, maintaining highest product quality, safety, performance and reliability..
- Lead System, sub system and component level engineering design activities by the team, ensuring all technical, quality, safety and reliability requirements are met.
- Ensure DFM, DFA and DFS principles are taken care during design phase.
- Ensure required standards of documentation compliant with the QMS and regulatory requirements are maintained including DHF as well as submission documents for product certification by FDA and other regulators.
- Manage change control, obsolescence management, impact assessment, Supplier change notifications and related documentation for product sustenance.
- Systematic approach towards understanding customer requirements, ideation, technical feasibility assurance, risk identification & mitigation, engineering design & development, component / sub-system / System level testing & integration of complex design concepts and analysis of technologies that incorporate own area of expertise.
- Work effectively with cross functional teams including quality, program management, manufacturing, regulatory, medical and clinical for effective implementation of qualification and certification strategy.
- Collaborate in establishing processes for effective resource management from planning through execution in close collaboration with program management.
- Responsible for development of state-of-the-art industry expertise and technical competencies for the team.
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