Description

About the job

Key Responsibilities:

• Experience of 4-7 years in Medical device industry.

• Exposure to good Documentation Practices and understanding of Design input/ Output/ Verification deliverables.

• Exposure to EUMDR or regulatory requirements will be an added advantage.

• Exposure to new technologies and current industry practices are expected

• Quick learner and should be able to deliver with minimum intervention.

• Good verbal and Written Communication Skills.

 

Qualification and Experience:

• Bachelor’s Degree in Mechanical Engineering or Equivalent Engineering Degree.

• Experience in Sustaining, Remediation, and New Product Development projects and their documentation in different phases is essential.

• Experience in ECO/ ECN routing will be an added advantage

• Experience and exposure to manufacturing/design/ testing of the medical industry will be an added advantage

• Knowledge of CAD like SolidWorks, CreO, and PLM tools is expected.

Education

ANY GRADUATE