Quality Control enthusiast with a flair for IT Systems

We save lives worldwide; Would you like to join us?

We are currently seeking a highly motivated and experienced individual to join AJ Vaccines as a QC Professional specializing in IT System integration. In this role, you will be pivotal in our global mission to save lives worldwide by designing and implementing our new Laboratory Information Management System (LIMS), while ensuring adherence to strict regulatory requirements.

What does it take? A keen interest in IT systems and preferably a familiarity with and knowledge of LIMS (Laboratory Information Management System) and GxP (Good x Practice) principles. Further, the position requires good decision-making abilities and a proactive mindset to drive progress even in the face of challenges. If you hold a deep understanding of business complexities, enjoy working independently immersed in detail, and are passionate about making a meaningful impact, we encourage you to apply and be part of our dedicated team at AJ Vaccines.

 

Team responsibilities and ambitions
You will be a key member of our LIMS Implementation Project Group, reporting directly to the Head of QC-SAM (Sample Management). We are implementing LabVantage as our LIMS system, and you will work closely with the LIMS team to design, develop, and implement this new LIMS system. The project management team also includes a LIMS Architect who will provide you with guidance and support throughout the project.

Our ambition is to establish a robust and scalable LIMS system that will streamline our laboratory processes, improve data quality, and enhance regulatory compliance. We are committed to delivering an IT solution that will support our growth and success, and your contribution will be vital in fulfilling this commitment.

 

Your work tasks
You will be responsible for implementing and supporting the design of our LIMS system, by creating and maintaining the Master data that forms the backbone of our LIMS, which aligns with our strategic objectives and regulatory requirements.

Together with the project team, you will be responsible for:

  • Support, design and implement LIMS modules
  • Create and maintain LIMS Master data such as test methods, sample types, instruments, users, and equipment
  • Create and maintain the end-to-end flow of QC methods in LIMS
  • Conducting quality checks
  • Participate in User Acceptance Testing (UAT) as well as validation activities to ensure that the Master data is complete, accurate, and meets the needs of the users
  • Document LIMS procedures
  • Train end users

 

Who are you?
We envision our future colleague as a highly motivated, proactive individual with an academic background and hands-on experience in LIMS or similar GxP systems. You should also have a strong understanding of data integrity and quality control procedures with the ability to work independently as well as collaboratively within a team.
 

Qualifications:

  • Prior hands-on experience with LIMS or similar GxP systems, preferably as a Master data/Static data builder
  • Familiarity with front-end LIMS
  • Fluency in both written and spoken English and Danish
  • Hold at least a bachelor's degree in IT, Natural Science, Engineering or a related field
     

Nice-to-have experiences:

  • LabVantage experience
  • Knowledge of equipment and analytical method qualification
  • Familiarity with other laboratory software applications


Personal traits:

  • Curious and detail-oriented
  • Proactive and self-driven
  • Ability to troubleshoot complex problems
  • Proficient in clarifying intricate issues and communicating technical concepts to non-technical stakeholders
  • Confidence in decision-making
     

We offer
An exciting and challenging job in a company with high professionalism where you will work in a collaborative environment with a team of talented and motivated professionals. This position enables professional growth and development, making a positive impact on the company’s operations and the lives of patients.
 

Interested?
If you are excited about the opportunity to join our team and make a real difference, we encourage you to submit your application as soon as possible. We will continuously review applications and invite candidates for screening and interviews. We are committed to a fair and inclusive recruitment process, which is why we prefer applications without photos.
 

If you have any questions or need further information, please contact Sr. Manager Susanne Stybe Aarup on +45 7229 7188 or SAA@ajvaccines.com. You can also reach out to our TA partner David Eskelund via email DAES@ajvaccines.com.

We look forward to reading your application!

Become a part of AJ Vaccines 
From our headquarters in Copenhagen, we develop and manufacture vaccines, diagnostics, and therapeutic solutions for the world. We are proud to contribute to disease control in more than 50 countries through our collaboration with WHO and UNICEF. We have more than 600 colleagues, and we pride ourselves on being a diverse workforce with passports from 37 nationalities.
 
Being part of AJ Vaccines means joining a common mission towards a healthier and safer world. Whether you're an experienced professional or an emerging talent, you'll find a platform here to contribute, innovate, and create meaningful change.

Application due


Start date
Start as soon as possible

Work hours


Position category


Position type

Workplace
Copenhagen S

Contact
Susanne Stybe Aarup 
 
 
 
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