Ensuring the proper manufacture and release of medical cannabis
Fulfilling duties as a Qualified Person in accordance with §15 of the German Medicines Act (AMG)
Acting as the Responsible Person under the Medicinal Cannabis Act (MedCanG)
Providing consultancy and training to cannabis companies within and outside Europe
Liaising and coordinating with the relevant authorities
Supporting and further developing quality standards and processes

University degree in Pharmacy, Chemistry, or Biology
At least two years of practical professional experience in pharmaceutical quality assurance, production, or quality control
Thorough knowledge of Good Manufacturing Practice (GMP) and regulatory requirements in the pharmaceutical industry
Strong sense of responsibility, analytical skills, and decision-making ability
High level of initiative and the ability to work independently
Excellent communication skills
Business-fluent German and English, both written and spoken
Permanent residence in Germany
Willingness to undertake regular business travel within Germany
Willingness to travel occasionally worldwide (approx. 2–5 times per year)
Clean criminal record (does not need to be submitted with the application)

Senior Consultant

Key skills