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.

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:

• Jacob Christian Voss, Pharmaceutical Specialist: +45 30833347
• Kirstine Høeg-Møller, Senior Director: +45 30833598

Applications must be received by 28. September 2025.
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.

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:

• 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.