• Dynamic MedTech environment with strong regulatory standards
• Strategic and hands-on leadership exposure

Firmenprofil

Our client is an established and growing international company operating in the medical devices industry, with manufacturing activities in Switzerland. The organization is recognized for its strong quality standards, innovation, and commitment to regulatory compliance.

Aufgabengebiet

• Act as Quality Management Representative for a certified and harmonized QMS across multiple sites
• Lead and manage QA teams across two production locations, including resource planning and development
• Ensure compliance with international regulations and standards (e.g., ISO 13485, FDA requirements)
• Oversee key quality processes such as CAPA, complaints handling, change control, and audit management
• Plan, lead, and follow up on internal, external, and regulatory auditsServe as the ma...