GMP Packaging Specialist, Finished Goods Production

LUNDBECK
Copenhagen, Region Hovedstaden
for 6 dage siden

GMP Packaging Specialist, Finished Goods Production

Are you passionate about creating an environment where quality, compliance, and production efficiency go hand in hand? Do you have a solid understanding of GMP requirements and experience in Finished Goods Production?

If so, you could be the ideal candidate to join us as a GMP Packaging Specialist, where you'll help ensure that high-quality standards are met without compromising production performance.

Your new role

In this dynamic and independent role, you will be part of a collaborative and supportive team, working alongside skilled colleagues in a positive and engaging environment.

As a GMP Packaging Specialist, you will play a key role in supporting Lundbeck’s pharmaceutical production by executing quality-related tasks, driving root cause analysis, and contributing to GMP improvement projects. With a structured and data-driven approach, you will work closely with cross-functional teams to identify opportunities that enhance both compliance and production efficiency.

Key responsibilities include:

  • Providing first-line GMP support to production
  • Ensuring high standards of quality and compliance through a continuous improvement mindset
  • Creating and reviewing quality-related documentation, including SOPs, deviations, complaints, and change requests
  • Participating in regulatory inspections and internal audits
  • Taking part in complex, high-impact projects, offering guidance to stakeholders to ensure alignment with GMP and operational goals

Your future team

You will be joining the Production GMP Support team, made up of seven skilled and dedicated colleagues who provide essential support to Finished Goods Production. The broader Finished Goods Production department consists of approximately 100 employees, all working together to ensure the delivery of high-quality pharmaceutical products.

Until a new reporting structure is established, you will report directly to the Senior Director of Finished Goods Production.

The position is based in Valby, Denmark.

What you bring to the team

  • An academic degree in Pharmaceutical Sciences, Engineering, or a related field
  • Over 5 years of relevant experience within Finished Goods Production, preferably with a focus on GMP-regulated packaging processes
  • Strong knowledge of GMP requirements according to EudraLex and FDA guidelines, ensuring compliance in all packaging activities
  • Demonstrates role model behavior by consistently upholding GMP standards, fostering a culture of quality and integrity, and always seeking to benefit production within established quality frameworks
  • Strong collaboration skills and an analytical, solution-oriented mindset
  • Experience with Operational Excellence and LEAN methodologies
  • A natural curiosity and a proactive approach to engaging with colleagues, stakeholders, and understanding the broader business purpose
  • Flexibility and adaptability in handling changing tasks, priorities, and workflows
  • A high level of accountability and ownership in your area of responsibility
  • Proficiency in both written and spoken Danish and English

As a person, you are known for your positive mindset and solution-oriented approach. You understand when to be pragmatic and when to firmly uphold requirements. You are a true team player who brings a can-do attitude to the office, even during busy periods.

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.


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.


If you have questions, please contact Senior Director, Abilashan Padmanathan on +45 30 83 43 15.


Applications must be received by August 10th, 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.

About Lundbeck

At Lundbeck, our most important contribution is easing the burden of the millions of people living with brain disorders. Whether it is migraine, depression, or other brain disorders, patients, their carers, and society as a whole depend on us.

Through cutting edge science and strong partnerships, we develop and market some of the world’s leading treatments, expanding into neuro-specialty and neuro-rare from our strong legacy within psychiatry and neurology.

The brain health challenge is real. Our commitment is real. Our impact is real.

Apply
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