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Senior Medical Writer

Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?

As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.

Senior Product Test Engineer - Medical Devices

Do you want to design safe and reliable medical devices, bringing our clients' life-changing solutions into the hands of patients and helping patients to get better treatment?

You will be an essential contributor in the development and designing optimal verification methods for requirement confirmation.

We seek to enable the best work environment that helps you and the business work together to produce superior results.

Fødevarespecialist for kvalitet, sikkerhed, bæredygtighed og innovation

Som Fødevarespecialist vil du indtage en central position, hvor du vil arbejde med kvalitet, HACCP, bæredygtighed og innovation. Rollen kræver innovativ tænkning, strukturerede arbejdsgange og stor grad af tværfagligt samarbejde i organisationen og værdikæden.

Opgaver:

Dine primære arbejdsopgaver vil omhandle kvalitet, HACCP, bæredygtighed og sikring af daglige kontroller. Du vil arbejde i et team, som består af forskellige afdelinger, der alle har et fælles ansvar for at sikre samhørighed på tværs i organisationen. Du har ansvaret for fødevaresikkerheden.

Senior Engineer Device Manufacturing

Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?

Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.

QA Specialist

You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.

You will have the opportunity to:

• Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
• Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.