Advanced Manufacturing Engineer at Vicarious Surgical

Bengaluru, karnataka, India -

Full Time

Start Date

Immediate

Expiry Date

02 Jul, 26

Salary

0.0

Posted On

03 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Manufacturing Engineering, Design for Manufacturing, SolidWorks, Process Validation, Statistical Analysis, DOE, Gage R&R, PFMEA, Medical Device Quality Systems, ISO 13485, 21 CFR Part 820, Tooling Development, Fixture Development, Failure Analysis, Project Management, Prototyping

Industry

Medical Equipment Manufacturing

Description

Vicarious Surgical is seeking an Advanced Manufacturing Engineer to join our team in Bangalore, India. You will work with R&D and Manufacturing engineers to drive design for manufacturing and assembly activities during all phases of development. Vicarious Surgical is a US based next generation robotics company developing a disruptive technology with the goal of increasing the efficiency of surgical procedure, improving patient outcomes, and reducing healthcare costs. This is a terrific opportunity for an engineer to join our company at a very exciting time and be a key member of a team of mission-driven and kind individuals with diverse experiences to lead Vicarious into its next phase of market disruption. This individual will be employed by a Professional Employer Organization (PEO), but doing work specifically for Vicarious Surgical. Working hours of Monday through Friday (Office hours start at 3PM to ensure significant overlap with US hours) Responsibilities: Design, development, and validation of new robust manufacturing processes. Major contributor in product teams supporting design for manufacturing elements and ensuring process capabilities meet targets for all design specifications. Provide product and process DFM (Design for Manufacturing) recommendations to product development core team to enhance manufacturability and reduce product cost. Design, construct and validate assembly, manufacturing, and test equipment. Provide requirements input to R&D to ensure product and equipment design meets quality, ergonomic, safety, and cost and throughput. Assess process capabilities, prioritize process improvements opportunities, and innovate and implement process improvements that meet quality, ergonomic, safety, cycle/TAKT time and cost targets. Lead the development of PFMEA’s and the development and execution of MFG. test and validation plans. Perform process capability analysis, failure analysis for discrepant production components, assemblies, or field returns, and troubleshoot manufacturing line issues. Support manufacturing team in maintaining compliance with medical device quality system requirements, including corrective/preventive action closure, disposition of non-conforming materials. Provide training or assist in training of production staffs for assembly, testing, and the use of new released equipment, methods, and procedures. Work closely with suppliers to ensure purchased components and assemblies meet requirements and support production volumes. About You BS degree in Mechanical, Electrical, Biomedical, Materials Engineering or equivalent degree is required. 5-10+ years of manufacturing engineering experience in a highly regulated industry; medical device company experience - preferred. Working knowledge in statistical analysis, DOE’s, Gage R&R’s, capability studies and process validation essential. Experience developing and implementing manufacturing assembly processes. Medical device capital equipment and single use disposable product experience - preferred. Strong technical skill in SolidWorks, prototyping, tooling/fixture development and troubleshooting. Hands-on proficiency with machine shop tools and 3D printers. Solid understanding in materials, BOM structure, and best practices for complex device assembly. Demonstrated experience with process validation planning/execution, IQ/OQ/PQ protocols, and reports. Solid experience transferring products from R&D to manufacturing. Excellent knowledge of 21 CFR part 820 and ISO 13485. Excellent project management skills. Together, we share a love for learning and we are passionate teachers. As a company, we set ambitious goals and individually, we share in that ambition.

Responsibilities

The Advanced Manufacturing Engineer will design, develop, and validate robust manufacturing processes while collaborating with R&D to ensure design for manufacturing standards. They will also lead failure analysis, manage process improvements, and ensure compliance with medical device quality system requirements.