Senior Design Engineer

PowerToFly; Gurgaon; On-site; INR 1,200,000 - 1,500,000; Full time

Job summary

A global healthcare company is seeking a skilled engineer to develop and verify components for medical devices in Gurgaon, India. You will be responsible for translating design inputs into specifications, conducting complex research, and collaborating with various teams to ensure project success. Candidates should have 5-7 years of experience in medical device development, a strong understanding of CAD software like CREO and Solidworks, and a proven ability to handle advanced technical tasks with minimal supervision. This role offers a hybrid work model.

Qualifications

• 5-7 years of experience in medical device development.
• Ability to work under minimal supervision.
• Strong problem-solving skills in technical projects.

Responsibilities

• Research and develop components/modules for medical devices.
• Translate design inputs to engineering specifications.
• Collaborate with R&D, Quality, Manufacturing, and other teams.

Skills

Medical device experience

Good CAD working knowledge - CREO and Solidworks

Drawing creation and interpretation

Job description

Work Flexibility: Hybrid

What you will do:

Technical Responsibilities:

• Under minimal supervision, research, design, develop, modify, and verify components/modules for medical devices
• Translate design inputs to engineering specifications and produce sub-system level designs Develop and analyze solutions, prototyping one or more options to provide proof of concept
• Apply fundamental and some advanced concepts, practices and procedures for problem solvingBusiness Responsibilities: Demonstrate advanced understanding of customer needs and design inputs Demonstrate proficiency with products intended use and clinical procedures
• Learn how the financial models are constructedMed Device Compliance: Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements Independently create or refine engineering documentation, such as the Design History file
• Follow R&D procedure like design controls and risk management, per the Quality Management SystemGeneral Responsibilities: Under minimal supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success Quickly process and assimilate procedures, policies, processes, systems, and technology required
• Work on complex problems, applying advanced experience and learnings Demonstrate ownership and prioritize work with minimal supervision
• Works as key member of the team, collaborating with others and solidifying relationships

What You Need:

Required Skills:

• 5-7 years of experience, medical device experience
• Good CAD working knowledge - CREO and Solidworks
• Drawing creation and interpretation understanding
• Under minimal supervision, research, design, develop, modify, and verify components/modules for medical devices

Preferred Skills:

• Translate design inputs to engineering specifications and produce sub-system level designs
• Demonstrate proficiency with products intended use and clinical procedures
• Develop and analyze solutions, prototyping one or more options to provide proof of concept