/ L'annuaire des offres d'emploi en Suisse Romande
n/a n/a Fribourg CH
full-time

Quality Manager - MedTech environment

Entreprise
Michael Page Switzerland
Lieu
Fribourg
Date de publication
02.06.2026
Référence
5251475

Description

We are looking for a Quality Manager to oversee and develop a harmonized Q
Quality Manager - MedTech environment (m/f/d)
We are looking for a Quality Manager to oversee and develop a harmonized Quality Management System across two production sites in a regulated MedTech environment. This role combines operational leadership, regulatory compliance, and strategic quality oversight with direct team management responsibilities.
Quality Manager - MedTech environment (m/f/d)
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.
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 ( , 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
Profile
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
Job 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 jid9a51769afr jit0623afr jpiy26afr

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