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QA Manager Site Denmark, Global Quality

Agilent Technologies Denmark-Glostrup Publiceret 30. sep. 2026 Agilent CareersPersonaleleder
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Resumé

Leads the Manufacturing QA Qualification and Validation team at the Denmark site, overseeing quality, regulatory compliance, audits, and continuous improvement. The role also represents QA management in strategic projects and supports collaboration across manufacturing and other functions.

Læst af AI
Læst fra jobopslaget af AI. Arbejdsgiverens egne felter vinder altid.

Kort om jobbet

Employment type: Full time. Requisition: 4039736. Country: Denmark. Job Description As Manager in Manufacturing QA, you will be leading a team 7-10 of highly engaged and skilled QA engineers and specialists to ensure quality as well as regulatory compliance within manufacturing processes in production of intermediates to finished products of our Invitro Diagnostic medical devices and accessories.

You will work as part of the Glostrup QA management team in close collaboration with stakeholders include Manufacturing, Regulatory Affairs, Research and development and Procurement, covering processes from design transfer of new products to release of our marketed products for invitro diagnostic of cancer.

The role offers a unique combination of strategy, execution, transformation, and people leadership, providing significant visibility and influence across the DK site and the broader Agilent enterprise to align processes across manufacturing sites. Position Summary We are seeking an experienced and inspirational leader to head the Manufacturing QA Qualification and Validation team.

You will be representing QA management in project steering groups as well as setting direction and coaching team members to ensure product quality, patient safety and compliance to internal and external requirements1 …

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