Live opening · Posted 3 days ago

Senior Mechanical Engineer

SolidPro - HelixA · Chennai, Tamil Nadu, India (On-site)
Linkedin No
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At a glance

The key details from the original listing.

Posted 3 days ago
CompanySolidPro - HelixA
LocationChennai, Tamil Nadu, India (On-site)
Work modeNo
SourceLinkedin
ListedPosted 3 days ago

About the role

Description supplied by the original job listing.

Job Description | Senior Mechanical Engineer
Location | Hyderabad
• Strong proficiency in 3D CAD software (e.g., SolidWorks, Creo, or AutoCAD) and experience with finite
element analysis (FEA) tools.
• Experience working with vendor partners on R&D projects, assisting in performance tracking, SLA
monitoring, and supporting demand planning to ensure alignment with project requirements.
• Familiarity with medical device product lifecycle management, with experience in applying FDA Design
Controls and international standards (e.g., 820-CFR, ISO14971, IEC60601), ensuring compliance with
project-specific regulations.
• Experience in supporting project and program management efforts, with a focus on managing day-to-day vendor partner interactions, driving continuous improvement in engineering processes, and contributing to
team growth.
• Comfortable working in Agile SCRUM and stage-gate environments, ensuring collaboration with
cross-functional teams to meet project objectives.
• Ability to develop and contribute to design documentation, including CAD models, specifications, and
compliance records for manufacturability and quality assurance.
• Knowledge of materials compatibility, durability testing, and mechanical design principles, contributing to design solutions to mitigate risks.
• Understanding of manufacturing processes for mechanical components, including injection molding,
machining, and rapid prototyping, and experience with managing design for manufacturability.
• Experience with requirements management systems (e.g., DOORS, JAMA), contributing to risk analysis
and DFMEA processes in mechanical R&D projects.
• Effective stakeholder management skills, collaborating with PMO teams to ensure technical alignment
and timely project delivery.
• Experience working with project data, contributing to technical assessments and identifying opportunities for process improvements and operational efficiency.
• Strong communication skills, with the ability to present technical updates and information clearly to cross-functional teams and stakeholders.
Education
• A degree or higher qualification in Biomedical / Mechanical Engineering from a recognized university.
• Masters in biomedical / Mechanical engineering or business will be an added advantage.
Experience
• 6-10 years of experience in Mechanical Engineering R&D in the medical devices domain, with a strong
technical knowledge.
• Proven experience in collaborating with PMOs and global teams on mechanical projects.
• Strong technical background in mechanical design, circuit board development, and compliance with
regulatory standards.
• Experience with design for manufacturability (DFM) and design for assembly (DFA) principles.
• Experience in medical device development.
Required Skills
• Strong technical expertise in mechanical engineering, materials science, and product design, with
hands-on experience in R&D and/or sustaining engineering, especially in product development
environments.

Work arrangement
No

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