Technical Writer

Join our team and help bring life-changing pen needles to patients around the world as a Technical Writer at our Needle Manufacturing & NPI site in Hjørring.

In this role, you will be the bridge between technical experts, regulatory affairs, and global affiliates, translating complex matters into clear, structured documents that move our projects forward. You'll work on a variety of projects, gathering knowledge and facilitating meetings to ensure precision and clarity in your writing.

Your day-to-day tasks will include:

• Planning, managing, and preparing change requests, standard operating procedures, protocols, and reports
• Drafting submission documents for applications to health authorities
• Facilitating meetings to capture the right inputs from product experts and project managers
• Collaborating with regulatory affairs and affiliates across the global network
• Ensuring documentation aligns with quality standards and regulatory requirements (e.g. MDR)
• Maintaining oversight of multiple tasks and keeping stakeholders aligned on progress

Your new department

In Global Manufacturing & Supply, we are dedicated to supplying life-saving medicines to patients across the globe. As part of the Process Intelligence & Validation team, you'll work with colleagues responsible for establishing production equipment, manufacturing development, and validation activities at our Hjørring site.

We are part of Needle Manufacturing & New Product Introduction (NMN), where we focus on the assembly and packaging of pen needles, as well as quality control hub for all pen needles across our network. NMN also supports new device development and ensures a stable supply of high-quality pen needles for patients in need.

Your skills & qualifications

We are looking for a structured communicator with the following qualifications:

• An M.Sc. in science, technology, or medical science
• Experience as a technical writer in the pharmaceutical industry
• Strong communication skills and the ability to explain complex matters in a simple, accessible way
• Fluency in written and spoken English
• Attention to detail and ability to manage multiple tasks and stakeholders
• Experience with documentation according to MDR requirements is a plus

Working at Novo Nordisk

At Novo Nordisk, you will be part of a company focused on lasting change for long-term health. You'll join a culture of constant curiosity, diverse thinking, and extraordinary results. Continuous learning, career development, and benefits are all part of the package.

What we offer

For this role, the Annual Base Salary ranges from 499,600 to 734,400 DKK. Incentives and benefits may also be included based on position level, location, and relevant market benchmarks.

More information

For further information, please contact Senior Manager Malene Eberhardt Mølbak at MWQA@novonordisk.com.

Deadline

Applications are reviewed on an ongoing basis with a deadline of 5th July 2026.

To ensure an efficient and fair recruitment process, please refrain from adding a photo in your resume. Novo Nordisk is committed to an inclusive recruitment process and equality of opportunity for all applicants.

Join us in creating lasting change for long-term health and be part of a legacy that spans generations.