• Bachelor’s degree in Engineering, Life Sciences, or a related field (completed or in progress).
• Proven experience in supplier quality, preferably in the medical industry.
• Knowledge and experience in ISO 13485.
• Experience in validations and understanding of basic related concepts.
• Advanced English (spoken and written).
• Ability to work independently and as part of a team.

Desirable:

• Experience in managing remediation issues and communication with suppliers.
• Project management and problem-solving skills.