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Quality Manager - MedTech environment (m/f/d)

Michael Page Fribourg, FR permanent

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Description du poste

* Dynamic MedTech environment with strong regulatory standards * Strategic and hands-on leadership exposure ## About Our Client ## 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. ## Job Description ## * 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 audits * Serve as the main point of contact for quality-related topics towards customers, authorities, and partners * Monitor QMS performance and report on key quality indicators to senior management * Drive continuous improvement initiatives across the organization * Collaborate on regulatory topics and support cross-functional projects ## The Successful Applicant ## * Technical background with further education in Quality Management * Minimum 3 years experience in Quality Assurance within a regulated MedTech manufacturing environment * Previous experience managing teams * Good understanding of regulatory frameworks and quality standards * Experience or exposure to Regulatory Affairs is an asset * Strong interest in technical topics and continuous improvement (Lean mindset is a plus) * Effective communication skills, with the ability to interact with multiple stakeholders * Familiarity with MS Office and quality/ERP systems * Fluent in French and/or German, with a good command of English ## What's on Offer ## * A key leadership role within a high-quality, regulated environment * Exposure to both operational and strategic challenges across multiple sites * The opportunity to influence quality strategy and continuous improvement initiatives * A collaborative and international work environment Quote job ref JN-052026-7025097 Job Function Engineering & Manufacturing Specialisation Quality Industry Healthcare / Pharmaceutical Location Fribourg Contract Type Permanent Job Reference JN-052026-7025097

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