Key Responsibilities:

- Design and develop new medical devices or plastic components using CREO / SolidWorks.

- Prepare and review engineering drawings, 3D models, and BOMs as per design standards.

- Manage and implement Engineering Change Requests/Notices (ECR/ECO/ECN) for design updates.

- Support design verification and validation activities, including DFMEA, risk assessment, and testing documentation.

- Prepare design history files (DHF), technical documentation, and ensure compliance with CE/FDA design control requirements.

- Participate in prototype development, testing, and design reviews.

- Ensure all product designs meet quality, safety, and regulatory standards.

- Continuously improve design processes and support cost reduction/efficiency projects.

Required Skills & Competencies:

- Proficient in CREO or SolidWorks (mandatory).

- Sound understanding of product design, GD&T;, DFM, DFA, and tolerance analysis.

- Experience in ECR/ECN processes.

- Knowledge of medical device design and relevant regulatory requirements (ISO 13485, CE, FDA) preferred.

- Solid problem-solving, analytical, and documentation skills.

- Good communication and teamwork abilities.

📌 R&D Engineer (Faridabad)
🏢 Polymed
📍 Faridabad