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Safety Manager to the IC5-programme

Your future 30 colleagues look forward welcoming you in the Technical department.

Our primary task is to deliver well-functioning trains and maintenance, contributing to a greener Denmark. In the project you contribute to ensure that the supplier comply to our safety requirements, which will lead to the rolling stock being authorized by the relevant authority.

We offer the possibility of working from home up to two days a week.

Supplier Quality Assurance (SQA) Engineer

Just a kitchen, some might think. But at Nobia, we recognise its deeper essence. It's more than a space - it's the very soul of a home where mornings are greeted, and evenings wind down.

You will support Sourcing, Product Management and Sustainability with the development, implementation, and management of processes which ensure Nobia Suppliers are approved and continuously developed and improved

QA-specialist, der er QP-delegeret eller drømmer om at blive det

Drømmer du om at bidrage til at sikre kvaliteten af livsvigtige lægemidler, der redder liv? Er du en erfaren kvalitetsspecialist med erfaring fra lægemiddelproduktion?

Som delegeret Qualified Person (QPd) i vores Manufacturing QA (MQA) afdeling får du en unik mulighed for at arbejde med kvalitetssikring og frigivelse af Xellias produkter. Du vil være med til at sikre, at vores antibiotika når frem til patienter i hele verden i den højeste kvalitet. Som delegeret QP hos Xellia får du et stort ansvar.

Process Engineer

The Process Engineer will be responsible for process engineering and technical support of Tetra Pak capital projects, as well as specification of equipment and functional design within the given time and budgets.

You should be prepared to travel approximately 30% of your time to meet colleagues, customers and suppliers to fulfil the role (internationally, with extensive travel throughout North Europe & Benelux).

Regulatory Affairs Specialist

The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.

In this role, you will have the opportunity to:

• Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
• Ensure compliance with EU regulations.
• Generate STED files, international submissions & assess design changes.
• Plan and execute projects for new regulatory requirements.

Application Consultant

You will use your business acumen and collaboration skills to work with both management and shop floor operators to improve production processes and utilizing IT solutions for the manufacturing automation domain.

You will have domain knowledge of shop floor processes, and experience with Manufacturing Execution System (MES), Manufacturing Information Systems (MIS), database operator tasks, and common communication protocols used to interface production equipment.

Regulatory Affairs Manager

The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.

This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:

• Ensure regulatory compliance to maintain market approvals
• Lead a team of skilled RA associates
• Ensure alignment with relevant stakeholders

Lead Business Development Manager

Your primary responsibility is to spearhead business development initiatives aimed at identifying and developing profitable growth opportunities across the company's global operations in the CBS sector.

You will be responsible for crafting and executing growth strategies, translating them into real-world business opportunities that will improve growth and profitability for the company.