(Senior) Master Data Coordinator

(Senior) Master Data Coordinator

Do you want to work with master data that plays a key role in ensuring high-quality medicines reach patients worldwide? Do you thrive in a structured environment where precision, collaboration, and data quality matter every day? And are you curious about how AI and new digital capabilities may shape the future of master data? Then you could be our new colleague in Packaging Compliance Management & Master Data (PCM&MD).

Your new role

In this role, you will be part of the Master Data Operational team, where your primary responsibilities will include:

• Creating and maintaining master data for finished goods, bulk products, and packaging materials in SAP.
• Ensuring compliance with GMP and GXP standards in all master data processes.
• Supporting operational tasks related to change requests and cross-functional projects related to master data for new launches etc.
• Contributing to process optimization by identifying improvement opportunities and supporting automation initiatives.
• Maintaining and updating SOPs related to packaging compliance and master data to align with regulatory requirements.

Your future team

The work is primarily operational and centred around structured processes that ensure stability, compliance, and high-quality master data. Precision is key, as master data plays an important role in maintaining product quality and supporting the delivery of medicines to patients worldwide.

We are open to hiring either a Master Data Coordinator or a Senior Master Data Coordinator. At both levels, including Senior level, the role remains primarily operational. The Senior level will include more complex tasks, greater independent responsibility, and a higher share of cross-functional, project-related and process improvement activities.

As we are preparing for Assisted Master Data, you will join a team where AI and new digital capabilities are expected to influence ways of working and how we ensure high-quality master data.

We also offer flexibility to work from home up to two days per week.

The position is based in Valby.

What you bring to the team

We are looking for a candidate who can bring the following to the role:

• Experience in creating and maintaining master data, preferably in SAP.
• Knowledge of GMP/GXP standards and compliance requirements (experience in the pharmaceutical industry is an advantage).
• Knowledge of Supply Chain/Operations process flows
• A structured and detail-oriented mindset with a focus on quality.
• You thrive on managing multiple tasks simultaneously and confidently engage with diverse stakeholders across the organization.
• Curiosity and motivation to work in an area where AI and Assisted Master Data are expected to influence processes, ways of working, and data quality.

Fluency in Danish is required, as SOPs and procedures are in Danish.

You are a true team player with a positive attitude and a proactive approach to improving processes. You thrive in a busy environment and enjoy collaborating with colleagues and stakeholders across the organization.

Our promise to you  

Lundbeck offers an inspiring workplace and innovative culture, where our curiosity, accountability and adaptability enable us to transform lives. We want to go faster and further on addressing the big unmet needs of people living with brain disorders. We offer rewarding careers with a mix of exciting tasks and development opportunities that are balanced with initiatives focused on your well-being.

We need every brain in the game, and at Lundbeck, we are committed to building a workforce that is as diverse as the people we serve. Read more about our commitment at www.lundbeck.com/global/about-us/our-commitment/diversity-and-inclusion.

Annual base salary range: (582 000 - 799 700) DKK gross

At Lundbeck, we are committed to fair and transparent pay. Please note that the final base salary within the stated range will be based on relevant qualifications, skills, competencies, and level of proficiency as well as internal pay equity.

Apply now

Can you see yourself in this role? We want to hear from you. Does this sound like your dream job, but you’re not sure if you meet all the requirements? We still want to hear from you!

Upload your CV and include a few lines about your motivation for applying. We ask you not to include a photo or personal information that does not relate to your professional experience.

Applications must be received by August 10.

Learn more about us at www.lundbeck.com, LinkedIn or Instagram (@h_lundbeck).

#EveryBrainInTheGame

This job ad is intended for individuals seeking a career opportunity with Lundbeck. We engage with recruitment and search firms where needed on the basis of a written agreement, and we do not accept unsolicited requests of any kind. If you work as a recruitment consultant, you are kindly instructed to refrain from contacting Lundbeck or the hiring manager directly with suggested candidates. If you violate this policy, you do so at your own risk and for your own account, and Lundbeck will not assume any liability nor pay any associated fees resulting from such violation.