Job Description

Gi Life Sciences Basel seeks a dedicated Quality Systems Engineer consultant with 7+ years in medical device or pharmaceutical manufacturing. You will assess regulatory identity, manage technical documentation, and lead change control activities for DHTs under Roche SOPs.

Strong ISO 13485/IEC 62304 knowledge and CSV experience are required. That role involves coordinating with Product Management, Design Leaders and external manufacturers, plus upskilling teams new to medical device development.

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