Quality Assurance Specialist (f/m/d) 

Technical Operations | Vertanical | Denmark

Quality Assurance Specialist (f/m/d) 

Technical Operations | Vertanical | Denmark

Über uns / About us

The German based and internationally active FUTRUE Group is the incubator of tomorrow’s global health trends and innovations holding more than 20 companies worldwide, over 70 drug approvals and a diverse range of medical devices and functional foods. Above all, FUTRUE concentrates on the areas of medical cannabis, ground-breaking pain therapy, chemical-free pharmaceuticals, intelligent bacteria, dermaceuticals and e-health.

As a Danish subsidiary of FUTRUE, Vertanical Denmark ApS concentrates on and invests in the production, research and development of innovative cannabis varieties for pharmaceutical applications. The production plant in Marslev near Odense, Denmark, is a DMA-approved production facility for medical cannabis. Its visionary concept focuses on the highest hygienic standards and EU GMP guidelines for pharmaceutical production.

Deine Aufgaben / Your tasks

We are looking for a Quality Assurance Specialist (f/m/d) to strengthen our local QA-Team at helping Vertanical Denmark Aps to achieve its objectives.

  • You will be responsible for maintaining documents in the quality management system.
  • This includes change management and the follow-up of corrective and preventive measures.
  • You will manage, update, and improve SOPs and create logbooks.
  • Together with the full QA team, you continuously monitor the compliance with GMP regulations and ensure adherence to procedure.
  • You support the head of QA with planning, preparation, and execution of internal and external audits as well as the planning and execution of training courses (GMP, QMS).
  • As an expert, you are part of the batch review process and that every batch meets the registered pharmaceuticals requirements.
  • You will create, review, and execute Qualification/ Validation documents.
  • You will be responsible for keeping track of maintenance and calibration task.

Dein Profil / Your profile

  • You have successfully completed university studies in pharmacy, natural sciences, or you have a similar qualification.
  • You have knowledge of GMP regulations and current legislation (AMG, AMWHV).
  • An analytical, precise, and forward-looking working style, coupled with a creative approach, are a matter of course for you.
  • Previous, relevant professional experience in the field of quality assurance or quality control in a pharmaceutical company or a regulated work environment is a plus.
  • In addition to good communication and organizational skills, you also have very good written and spoken English skills, German is a plus.

Unser Versprechen / Our promise

We offer you a varied, challenging job with exciting tasks and a broad spectrum of creative possibilities! We offer an innovative environment for professional development with short decision-making paths and the freedom to break new ground!

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Telefon: +49 (0) 89 78 7979 0 - 873



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