பணி விளக்கம்

Overview

This role is for a Mechanical Engineer working on product development in a regulated environment. The position follows a hybrid schedule with 3 days on-site and 2 days remote each week.

Work Arrangement

Hybrid model: 3 days in the office and 2 days working remotely.

Required Qualifications

A bachelor’s degree in Mechanical Engineering is mandatory.
At least 3 years of hands-on mechanical engineering experience within a product development setting.
Practical exposure to the full Product Development Lifecycle (PDLM).
Experience conducting Design Failure Mode and Effects Analysis (DFMEA).
Background supporting design verification and validation efforts.
Strong capability in technical documentation and engineering change control.

Preferred Qualifications

Experience in the medical device industry is highly desirable.
Prior work in FDA-regulated or similarly controlled environments is a plus.
Familiarity with Creo for mechanical design and documentation is preferred.
Working knowledge of SAP, especially for engineering documents and document handling, is valued.
Exposure to Windchill would be an added advantage.

Key Responsibilities

Contribute to DSx product development work across the entire product lifecycle.
Facilitate and take part in DFMEA sessions and broader risk management activities.
Plan, carry out, and record verification and validation testing.
Prepare and update technical documents in line with quality and regulatory standards.
Work closely with engineering, quality, regulatory, and manufacturing stakeholders.
Investigate technical problems and support root-cause analysis.
Assist with design reviews and continuous improvement efforts.

Additional Information

This position is based in Queens County, NY. The role is full-time and remote/hybrid in nature. No salary figure, number of openings, or start date was provided.

Mechanical Engineer