Senior Quality Manager

As a Quality Manager in Operations, you will hold full end‑to‑end responsibility for the quality of all products delivered to our customers. You will oversee the evaluation and implementation of design changes, ensuring full compliance with applicable standards and product specifications. Your expertise will guide strategic decisions on product quality, risk, and business impact throughout the entire product lifecycle. 

In this key role, you will also coordinate activities across multiple production sites, ensuring consistent approaches to new product introductions, quality assurance, and non‑conformity handling across Diagnostics. 

What we offer:

• A chance to join a team of experienced and passionate experts in the diagnostics business. 
• Responsibility for shaping and developing the local quality organization at different levels. 
• A role where you can truly make an impact by sharing your expertise, influencing decisions, and contributing to strategic initiatives and projects. 
• A dynamic and supportive environment with space for both personal and professional growth. 
• Flexible working hours that support your work–life balance. 
• A Scandinavian work culture built on equality, openness, independence, and informal communication. 
• An attractive compensation package and strong development opportunities. 

Your responsibilities:

• Ensure all new product introductions and engineering change orders are supported by proper documentation and completed quality assurance activities before release to production. 
• Hold the authority to approve or reject design transfers to production. 
• Align and coordinate quality practices across Diagnostics production sites, ensuring products meet specifications and that supplier‑to‑shipment quality processes are followed. 
• Oversee execution of inspections in accordance with agreed inspection codes. 
• Maintain a strong connection between customer feedback and quality, ensuring complaints and major operational quality issues are communicated and addressed effectively. 
• Lead supplier quality assurance efforts and support purchasing in proactive initiatives. 
• Drive positive development of process KPIs and warranty‑related complaints within Operations. 
• Manage an effective CAPA process across all production sites. 
• Develop, update, and maintain QMS procedures related to Operations Quality. 
• Oversee departmental resources within company guidelines and managerial direction. 
• Develop and implement departmental strategies aligned with Diagnostics, Operations, and Global Quality & Regulatory objectives. 

What we hope you bring:

• Leadership experience in a global, multi‑stakeholder environment, ideally with teams or reports in different locations. 
• Minimum 5 years of experience in quality management; experience in the medical device industry is preferred. 
• Strong understanding of ISO 13485, MDR, FDA requirements, and global quality frameworks. 
• Demonstrated ability to assess risk and clearly communicate business impact. 
• Excellent analytical, documentation, and stakeholder‑management skills. 
• Fluency in English, written and spoken. 

In the role of Senior Quality Manager, you will collaborate closely with Flemming Vinding 

If you have additional questions, feel free to contact our recruiter Kasia: kmas@dgs-diagnostics.com 

Send your application and CV before 31 March 2026. Applications must be submitted in English via our application system. 

•    The interviews will be conducted on a rolling basis 

Additionally, please note that the company follows an internal reporting procedure available at: https://demant.codeofconduct.app/ 

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