Application Support Specialist

Visiopharm is a mid-sized MedTech company that specializes in transforming pathology through AI-based tissue analysis and standardization.

You will have many daily touchpoints with customers as you support them in maximizing the use of Visiopharm's products in their digital pathology analysis both within Research and Clinical fields.

You will become an expert in using our image analysis platform to its fullest capability and continue your training to be up-to-date with all new features.

TEMP Laboratory Technician

Are you passionate about starting your career as a laboratory technician, working hands-on to develop products that improve lives for people with intimate healthcare needs?

As part of our team, you will receive thorough training in a series of test methods and take part in developing new methods for upcoming projects alongside our Test Engineer team.

Development Engineer – Advance Materials Processing - DTU Energy

This position focuses on supporting the development of advanced ceramic and metallic components used in energy conversion devices, such as fuel cells, batteries, and electrolysis technologies, as part of the green transition.

You will play a key role in ensuring the smooth operation of key facilities, contributing to ongoing research and development projects, and providing hands-on support for process optimization and equipment development and maintenance.

Materials Engineering Specialist

As a Materials Engineering Specialist in our End Fitting Supply (EFS) department, you will engage in a variety of tasks that allow you to leverage your expertise and skills.

Your responsibilities will include:

• Implementing client and market requirements for metallurgy, polymers, and general materials, as well as their related industry processes.
• Reviewing project documentation and specifications to ensure compliance with mechanical and chemical property standards.

Supplier Quality Engineer

We are looking for a Senior Supplier Quality Engineer to join our team. The main responsibilities include ensuring compliance with various Regulations and Standards, leading Supplier Quality Compliance Projects, developing Partner Quality Agreements, managing high visibility SCARs, and conducting key Supplier Audits.

If you have expertise in Supplier Quality and a passion for process improvement, we want to hear from you!

Science Lab Tech Assistant / Laboratorieassistent (Skole)

Imagine a Grade 9 student lighting up when their experiment finally works - because the setup was flawless, the safety gear was in place, and the support was right there. That’s where you come in.

You’ll be the go-to person for lab logistics, equipment prep, and safety checks - enabling engaging, hands-on science lessons that inspire curiosity and confidence.

This is a part-time position (60-75 %, to be determined with the candidate).

QA Academic, Corporate Product Quality Assurance Biologics

Do you possess an analytical and data-oriented mindset? Are you motivated by problem-solving and finding new solutions to the way we work with skilled colleagues?

The team consists of 4 employees (3 academics and 1 technician) who are responsible for all commercial QA-related activities in connection with oversight of Lundbeck’s biological production at our CMO’s, as well as review and release to market for these products.

Platform Technician/Sr. Platform Technician

Are you a technician with a flair for library synthesis and lab automation? Then join the team in developing our groundbreaking next generation platform.

You will:

• Synthesize macrocycle libraries using advanced laboratory automation tools.
• Set up, operate, and maintain a variety of automated lab instruments, including peptide synthesizers, liquid handling systems, and analytical tools (e.g., LC-MS)

Your ideas and contributions will shape the future of medicine.

Principal Specialist - Design Control and Risk Management

Are you passionate about ensuring the highest standards of quality in medical devices? Do you thrive in a collaborative environment where your expertise can make a real difference?

As the Principal Specialist for Design Control and Risk Management, you will be responsible for the continuous support and development of our global quality processes across multiple business areas, including Ostomy Care, Chronic Care, Wound & Skin Care, Continence Care, Consumer Business, and Interventional Urology.