Technical Responsibilities
-
Under supervision, design, develop, modify, and verify mechanical components for medical devices
-
Assist with prototyping and bench testing
-
Support engineering, manufacturing and supplier changes by creating documents like ECO, MCO, ECRs etc.
-
Create or update engineering drawing, assembly plan, DHDs as per requirement.
-
Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements
-
Under supervision, conduct research and studies to support product design
Business Responsibilities :
Interpret customer needs and understands design inputs
-
Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirements
-
With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures
-
Learn R&D procedures like design controls and risk management, per the Quality Management System
General Responsibilities :
-
With supervision, work with R&D, Quality, Manufacturing, and Project Management to ensure project success
-
Learn procedures, policies, processes, systems, and technology required
-
Work on problems in limited scope; purposefully learn while gaining experience
-
Demonstrate ownership and integrity of work
-
Build stable relationships
-
Contribute to the project as a team member
-
Candidate should have good exposure to creating drafting/ manufacturing drawing in Solid works.
-
Candidate should have good Understanding of all design aspects and logics related to the design and manufacturing with hands on Solid works.
Tool Software Skill
-
Solid works is added advantage.
-
SPM (Special Purpose Machine) Skill set is mandatory.
-
Should have basic Microsoft office knowledge
-
Contact Person: Mr. Amit Kumar
-
Contact Number: +91 9560043049.
-
Email ID: [email protected]