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.
ANY GRADUATE