Specialist, Regulatory Affairs HUB DK

Abacus Medicine Group; København; On-site; DKK 550,000 - 750,000; Full time

Job summary

Abacus Medicine Group is seeking a Senior Regulatory Affairs Specialist to lead dossiers for parallel trading licenses and manage packaging materials. You will work in a structured, regulatory environment, ensuring compliance and timely market access across our markets.

You will collaborate with health authorities and external printers, monitor regulatory updates, and identify opportunities to improve processes.

Qualifications

• Master's or Bachelor's degree in Pharmacy, Regulatory Affairs, Life Sciences, or equivalent.

Responsibilities

• Prepare and submit dossiers to obtain and maintain parallel trading licenses.

Skills

QA/RA experience

Interacting with authorities

English proficiency

Independent decision making

Education

Master's or Bachelor's in Pharmacy/Reg Affairs/Life Sciences

Tools

Adobe InDesign

Illustrator

Photoshop

EULER braille tools

Text comparison software

Job description

Do you want to do more than simply maintain regulatory processes? Do you enjoy challenging existing ways of working, taking ownership, and finding smarter solutions? Join our Regulatory Affairs team and help us strengthen compliance, optimize processes, and ensure smooth market access in pharmaceutical parallel trade.

The opportunity

As our Senior Regulatory Affairs Specialist, you will be responsible for obtaining and maintaining parallel trading licenses and preparing packaging materials according to SOPs, WIs, and applicable guidelines.

However, this is not a role for someone who simply follows instructions.

We are looking for someone who is curious, proactive, and not afraid to challenge existing processes. Someone who sees opportunities for improvement, takes initiative, and actively contributes to making our ways of working even better.

You will be given a high degree of responsibility and the opportunity to influence both processes and standards within your area of expertise. Your work will ensure regulatory compliance, support efficient production processes, and contribute to timely market access across your assigned markets.

We Would Like You To

In this role, you will:

• Prepare and submit dossiers to acquire and maintain parallel trading licenses.
• Create and maintain packaging materials, artwork files, mock-ups, and item lists.
• Proofread packaging components, application files, and item lists to ensure accuracy.
• Manage and archive regulatory documentation, including packaging materials and authority-approved files.
• Communicate directly with health authorities and external printing houses.
• Monitor regulatory updates and implement required changes.
• Identify opportunities to improve processes, workflows, and documentation.
• Contribute to continuous improvement initiatives, training activities, and updates of working instructions and guidelines.
• Take ownership of your area and actively drive tasks from start to finish.

About You, Our New Colleague

We are looking for a detail-oriented professional who combines strong regulatory knowledge with a hands-on and solution-oriented mindset.

You enjoy working in a structured and regulated environment, but you also question how things are done and look for ways to improve them.

You are comfortable taking ownership, making decisions, and driving initiatives independently. You don't wait for someone else to solve a problem. Instead, you take the lead, involve the right stakeholders, and make things happen.

You Bring

• A Master's or Bachelor's degree in Pharmacy, Regulatory Affairs, Life Sciences, or an equivalent field.
• A minimum of two years of experience within the pharmaceutical industry.
• Professional proficiency in English (B2 level or higher).
• Experience in at least one of the following areas:
• QA or RA within the pharmaceutical industry.
• Interaction with regulatory authorities.
• Handling medicine forms and packaging materials in repackaging processes.
• Experience with repackaging processes and machinery.
• Proficiency in Adobe InDesign, Illustrator, and Photoshop, as well as knowledge of EULER (braille) and text comparison software.
• Good written and verbal communication skills in both English and the local language.
• Residence in the country where the role is based and a valid work permit.

Skills And Competencies That Will Make You Succeed

You have a solid understanding of regulatory dossiers, parallel distribution procedures, packaging material design, proofreading, and documentation management.

At The Same Time, You Are Someone Who

• Challenges the status quo.
• Identifies opportunities for improvement.
• Takes initiative instead of waiting for direction.
• Is comfortable working independently.
• Balances accuracy with efficiency.
• Enjoys creating structure and improving processes.

You understand that compliance and continuous improvement go hand in hand, and you are motivated by the opportunity to influence how things are done.

Our Recruitment Process

We value a transparent and efficient recruitment process.

• First interviews will be conducted online during week 38.
• Second interviews will take place in person at our office in Copenhagen during week 40.

We review applications on an ongoing basis.

Do you want to know more about us?

Moving Healthcare. Moving You.

In Abacus Medicine Group, you'll experience the power of Moving Healthcare. With our change mindset, we're moving the industry and improving healthcare as we broaden access to medicine.

But it's not just about moving healthcare, it's about Moving You. You'll be part of a caring community of more than 1,500 people across the World. With us, you will be valued, empowered, and have a direct impact on driving change. Let's access the future of medicine and make a difference together. Your move.