EXO ARNVIND is looking for a Manager for LIMS Superusers, for our customer, a World Leading vaccine company.

If you like to develop your leadership and project management skills within GMP IT systems, especially LIMS, and you are motivated by also being operational in the team with focus on developing, optimizing, and operating the LIMS system SampleManager (SM), this position will be perfect for you.

The position is located near Helsingør, Denmark.

Join our transformative journey

Our customer aspires to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system. They are a global leader in smallpox vaccines and their commercial product portfolio contains market-leading vaccines against rabies and tick-borne encephalitis as well as an Ebola vaccine.

They have embarked upon a truly transformative growth journey towards becoming one of the largest pure play vaccine companies by excelling in R&D innovation, manufacturing, and commercialization, and are looking for more talent to help drive the change.

Join their journey and change lives for the better all over the world

Dynamic team with a broad interface

In their QC department they handle a wide range of analysis for their Production as well as for their Manufacturing- and Process development departments. They are working under cGMP in close collaboration with their colleagues in the QC department in Germany. In Denmark they are around 55 employees in QC divided into seven teams: QC Biochemistry, QC Microbiology, QC Externals, QC Sampleflow, QC Stability, QC Raw materials, and QC SampleManager.

You will become part of and leader of a team of 4 dedicated SM-Superusers who all have Labtech background and extensive experience with SM.

You will report to the Snr. Manager for QC.

Leader for Super Users

Your main goal is to lead the team, and together with the team, to keep SM operational as well as finalizing SM projects within the agreed timeline while ensuring an engaging work environment. Your main areas of responsibility will be:

1. Handle technical and scientific issues within your group
2. Drive development within SM including prioritization, coordination, defining requirements, and test solutions
3. Secure close collaboration with stakeholders such as IT and Production and operational service within the QC department
4. Participate in SM projects
5. Together with Process Manager/Sr. SM-Superuser and Snr. Manager to prioritize and define projects and operations to follow the needs of QC
6. Ensure compliance with the quality system and cGMP in area of responsibility
7. Lead the team, including coordination of activities, ensuring deliverables, follow up, general supervision, resource planning, and training of team members

About you

We expect that you have the following experiences to succeed in the role:

1. Solid experience with LIMS
2. In-depth knowledge of pharma IT-systems
3. Scientific academic degree or similar
4. Solid GMP knowledge and experience is preferred
5. Excellent English

You thrive having the overview and you enjoy cross-department project cooperation as well as being able to help the team to focus and navigate efficiently between many tasks, projects, and priorities.

You take an active part in the daily operations while keeping up the team spirit and always aim for “working smarter not harder”.

Our customer offers:

A great career opportunity on the leadership path, in a growing leading vaccine company.

A chance to work in an international company with unique technology and a dedicated workforce. They offer a dynamic work environment and an opportunity to develop both your personal and academic competencies.

In addition, they offer an attractive salary package.

If the above descriptions could be you – then please apply here at OPEN POSITIONS

We look forward to hearing from you.

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