Mechanical engineer - Medical Product Design and Documentation Leameng Solution Technologies

5.0 - 9.0 years

0 Lacs

karnataka

On-site

As a Mechanical Engineer with 5 to 7 years of overall experience, including 3 to 5 years in the medical device industry, you will be responsible for utilizing your expertise in CAD software such as Solid Edge & NX, as well as conducting precise engineering calculations. Your proficiency in Geometric Dimensioning and Tolerance stack up analysis will be crucial for the successful execution of your responsibilities. You will be expected to demonstrate your ability to generate alternative mechanisms, concepts, and solutions, with a focus on designing for technical cost reductions. Moreover, you should be capable of performing theoretical calculations for the concepts developed, ensuring accuracy and efficiency in the design process. In this role, you will utilize existing tools and standard methodologies to effectively report and track product, project, and process metrics. Experience in the Design control process and DHF documentation for medical devices will be essential, and familiarity with EU MDD to MDR, Gap Analysis, and Risk Management and Analysis (including FMEA and Failure analysis) will be advantageous. Knowledge of Polarion software is preferred for this position. This is a full-time role with a day shift schedule and a yearly bonus. The work location is in person, and the application deadline is 18/07/2025.,

Posted 1 week ago

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Mechanical engineer Leameng Solution Technologies

5.0 - 9.0 years

0 Lacs

karnataka

On-site

As a Mechanical Engineer with 5 to 7 years of overall experience, including 3 to 5 years in the medical device industry, you will be responsible for utilizing your expertise in CAD software such as Solid Edge & NX, along with proficiency in engineering calculations. Your role will involve a strong command over GD&T and tolerance stack-up analysis to ensure precision in design. A key aspect of your responsibilities will be the ability to develop alternative mechanisms, concepts, and solutions, focusing on design for technical cost reductions. You will be expected to conduct theoretical calculations for the concepts generated, utilizing existing tools and standard methodologies to report and track product, project, and process metrics effectively. Experience in design control process, DHF documentation, and/or remediation for medical devices will be crucial for this role. Familiarity with EU MDD to MDR transition, Gap Analysis, Risk Management, and Analysis (including FMEA and failure analysis) will be advantageous. Knowledge of Polarion is preferred for this position. This is a full-time position that includes a yearly bonus. The work schedule is during day shifts, with the requirement to work in person at the designated location. The application deadline for this role is 18/07/2025.,

Posted 1 week ago

Apply

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