- Experience of 57 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 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:
- Bachelors Degree in Mechanical Engineering or Equivalent Engineering Degree.
- Experience in Sustaining Remediation and New Product Development projects and their documentation in in different phases are essential.
- Experience in ECO/ ECN routing will be added advantage
- Experience and exposure to manufacturing / design/ testing of medical industry will be added advantage
- Knowledge of CAD like SolidWorks CreO and PLM tools is expected.