Client: LEO Pharma
Location: Gdańsk, Poland
Job Category: Other
EU work permit required: Yes
Job Reference: ab9a3f7fefd2
Job Views: 22
Posted: 23.01.2025
Expiry Date: 09.03.2025
Application deadline: N/A
Contract type: Permanent
Job ID: 2271
Are you passionate about Clinical Supply management? Do you want to make a difference in a global organizational set-up ensuring our Investigational Medicinal Products arrive at site in time and at the highest quality standard? Then we might have just the position for you…
You will become part of LEO Pharma Clinical Supply Management. We are a team of five professionals dedicated to facilitating high quality clinical trial supply. We work closely with departments such as Clinical Project Management and Quality, Product Formulation & Support, Regulatory Affairs and more to ensure close collaboration and a smooth process.
“Our environment is rather fast paced and dynamic, yet it is very important to us to have a good work-life balance as we strongly believe that people in a good mental balance generate the best results. We think as one team, we handle challenges as a team, we win as a team, and we celebrate as a team.” – says hiring manager, Susanne Krogsgaard.
Our inclusive and diverse work environment fosters innovation, proactivity, and encourages professional growth. By joining us, you will contribute to a culture that values stakeholder focus, integrity, and trust.
An essential role for advancement of clinical trials & development of life-changing therapies.
Your responsibility entails independently planning and coordinating clinical supply activities for all development phases, both in-house and outsourced trials, including maintaining compliance with regulatory guidelines. You will also take on project responsibilities, ensuring collaboration between various departments and external vendors.
This is an opportunity to make a significant impact on the success of clinical trials and contribute to the development of life-changing therapies and have a central role in overseeing the management of clinical trial supplies.
Who are you?
We are looking for you who can bring hands-on experience with the following elements, as these will be central in this position:
Furthermore, we imagine that you have a degree in a relevant field (e.g., engineering, chemistry, pharmacy) combined with 5-8 years of experience in the pharmaceutical industry, including clinical supply management experience and knowledge of Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and Good Clinical Practice (GCP). Possessing professional proficiency in English, both written and spoken, will be vital.
Would you like to join our team?
We will be processing applications on a continuous basis, so apply via the online portal as soon as possible.
For additional information, please contact Susanne Krogsgaard, Manager for Clinical Process, Partnership and Supply, at (+45) 5365 8136. Kindly note annual leave July 6th – August 4th in this period please contact Andrea Olesen, Head of External Clinical Project Management (+45) 3120 5143. Kindly note annual leave July 18th – August 4th.
We hope to hear from you!
Beyond the skin
Join LEO Pharma, a global leader in medical dermatology, as we go beyond the skin to make a lasting impact. Our innovative approach sets us apart. We are dedicated to leaving a legacy that positively impacts patients, colleagues, and our planet.
At LEO Pharma, we believe in the power of individuals to drive change. Our flat organizational structure empowers you to make a visible impact and offers versatile roles for professional growth. We value diversity and welcome applications from all qualified candidates, recognizing that our different perspectives, backgrounds, and attitudes enable us to make the best decisions. Join our passionate team at LEO Pharma and be yourself as we work together to make a difference.
For certain positions, LEO Pharma might complete a background check conducted by a third party.
Join us on our journey Beyond the Skin. Apply today!
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