Pharmaceutical Scientist – GMP manufacturing
Do you want to play a key role in delivering innovative treatments to clinical trials?
Join Lundbeck as a Pharmaceutical Scientist with a focus on GMP manufacturing and be part of a team dedicated to improving the lives of people living with brain diseases. This is your opportunity to combine scientific expertise with GMP and regulatory requirements to make a tangible impact in the pharmaceutical industry.
Your new role
As a Pharmaceutical Scientist with a focus on GMP, you will support the clinical manufacturing of small molecule drug products in collaboration with Contract Manufacturing Organisations (CMOs), often based abroad.
Your key responsibilities will include:
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-Ensuring the timely delivery of materials for clinical manufacturing.
-Reviewing production documentation and ensuring compliance with GMP guidelines.
-Supporting investigations into deviations and resolving issues in collaboration with internal teams and CMOs.
-Applying your knowledge of dosage forms (e.g., oral solutions, capsules, and tablets) to define project-specific manufacturing requirements.
This position offers a unique opportunity to gain deep insight into GMP manufacturing, the R&D value chain, and the development interface of the pharmaceutical industry.
Your future team
You will join the Pharmaceutical Development team within Lundbeck’s Chemistry, Manufacturing & Controls (CMC) area, based in Valby.
Our team of 15 dedicated colleagues takes pride in combining scientific expertise with project-specific requirements to support clinical manufacturing. Our culture is built on curiosity, accountability and adaptability.
We work closely across roles to ensure the timely and compliant production of drug products, and we take pride in contributing to Lundbeck’s ambition to be #1 in brain health.
We value creativity and teamwork, and we make time to celebrate our successes and enjoy each other’s company.
The position is based in Valby, Denmark.
What you bring to the team
Our ideal candidate will have:
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-A MSc in Pharmaceutical Sciences, Engineering, or a related scientific discipline.
-A structured approach and a solid understanding of GMP requirements and regulations in the pharmaceutical industry with 2-5 years of experience. A positive mindset, a collaborative spirit, and the ability to embrace challenges.
-Fluency in spoken and written English.
-Insight into manufacturing processes for small molecules (an advantage). Experience working with CMOs or cross-functional teams will be considered a plus.
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 lundbeck/global/about-us/our-commitment/diversity-and-inclusion.
Apply now
Can you see yourself in this role? We 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.
If you have any questions, feel free to contact:
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-Jacob Christian Voss, Pharmaceutical Specialist: +45 #
-Kirstine Høeg-Møller, Senior Director: +45 30833598
Applications must be received by 28. September 2025.
Learn more about us at lundbeck, 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.
