What we are looking for

• Attention to detail, analytical, team player.
• Strong communication skills with the ability to interact with multiple stakeholders globally.
• Excellent written and technical writing skills.
• Patience, confidence, independence, and the ability to take control of tasks

Required skills

• Quality engineering and general engineering knowledge
• Familiarity with ISO 13485 and medical device regulations
• Experience in writing technical documentation
• Ability to support audits and think independently