QA Professional – Document Manager or GxP Documentation Specialist

Copenhagen

Pharmaceuticals/Biotechnology

Black Swans Exist recruits talents for UNION therapeutics 

Are you the one we are looking for? 

 

You want… 

To excel your skillset within quality assurance and documentation as part of UNION therapeutics A/S, an ambitious company that continues to be on an incredible growth journey. You’ll join the company at its most exciting stage so far in a newly established position. This means that you’ll shape your role and solve complex tasks during the development of innovative treatment options within immune-dermatology and anti-infective drug development. 

 

You will… 

Join Union’s ’can do’ environment and spend your time working with a mix of quality assurance, regulatory tasks, and documentation management. You’ll have variation in your work, and we guarantee that no two days will look the same. Consequently, you will utilize a wide area of your skillset rather than limiting your professional aspirations. While you’ll spend much of your time supporting QA reviews and implementing a new Document Management System, you are also going to become the go-to expert for EDMS in the UNION organization. 

 

You’ll join… 

UNION therapeutics A/S, a clinical-stage, diversified pharmaceutical company focused on identifying, developing and commercializing treatments for immunology and infectious diseases. Their current portfolio is comprised of two medicinal compound classes with well-characterized modes of action that hold significant potential to address unmet medical needs. UNION is based in Greater Copenhagen, Denmark. 

Behind UNION stands a highly successful team of experienced scientists who understand your professional profile and will support your further development. You will join a team of like-minded, competent peers who will guarantee dynamic challenges in a quantity you won’t find elsewhere. UNION values a non-bureaucratic environment that gives you the chance to act fast and freely with short decision-making processes. 

 

You have… 

  • 5+ years of experience in a similar role within pharmaceuticals 
  • First-hand experience with pharmaceutical production, QA, and/or regulatory affairs 
  • Knowledge of GMP/GCP requirements. 

Contact

If you want to hear more about this opportunity and the company, or if you have any questions regarding the position, please do not hesitate to contact us. If you wish to apply for the position, please send an updated version of your CV, together with what questions you might have, and we will get in touch with you soon.

TANIA CHAUHAN

Consultant

Talent engagement

apply now

* Please refrain from including your social security number (CPR no.) in your CV.

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