BETiC, IIT Bombay
Bachelor’s degree in Mechanical/ Production Engineering with 3 years of experience or equivalent.
Master’s degree in mechanical/ Production Engineering with 1 years of experience or equivalent.
Age: Less than 28 years.
Experience and skills
The candidate must have understanding of Mechanical product design, prototyping and testing.
Well versed with engineering mechanics, mechatronics principles, materials will be preferable.
Ability to understand customer, user requirements.
Expert at 3D Modelling software like SOLIDWORKS.
Good at hands on calculation of the design, quick prototyping and testing.
DFMEA and risk management.
Identifying the suitable material, Creating BOM, tolerance stack-up, GD&T.
Experience in different manufacturing processes and techniques of DFM/DFA.
Experience of managing a vendor network for manufacturing of prototypes.
Experience in latest engineering design and methods, tools, and processes.
Knowledge and understanding of ISO standards such as ISO 13485, IEC 60601 standards is preferred.
Good in understanding the design of experiments, testing methods.
Disciplined team worker, ability to work independently.
Ability to present ideas and to convince project team members.
Excellent communication skills and Team player.
Quality mindset in design and documentation.
Knowledge in injection molding, sheet metal design and conventional manufacturing processes.
Leading the entire project and relevant design and development of Medical Devices individually.
Product officer delivers specific operations to meet the requirements for medical device development
Define measurable design requirements, regulatory requirements for the project.
Lead in design, development, prototyping and testing of medical devices
Build 3D CAD models from engineering drawings or sketches for medical device assemblies, sub-assemblies, fixtures and tooling.
Prepare engineering drawings with tolerances and manufacturing plans.
Calculate parameters related to the design, quick prototyping and testing.
Create DFMEA and identify relevant product risks, risk management.
Identify suitable material, components, sub-systems, create BOM
Perform tolerance stack-up, GD&T.
Identify and use different manufacturing processes and techniques of DFM/DFA
Utilize equipment, tools, software’s, materials, components to convert design requirements to tangible design output in a collaborative environment
Interface between various stakeholders to ensure product safety and performance
Implement design and development activities as per ISO 13485, prepare medical device documentation.
Coordinate with industry partners, vendors, suppliers for manufacturing of prototypes.
Lead in design transfer activities to industries.
Disseminate knowledge and good practices through courses, events, demos, visits, exhibitions.
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