Ensuring the proper manufacture and release of medical cannabis
Fulfilling the duties of a Qualified Person according to §15 of the German Medicines Act (AMG)
Acting as the Responsible Person in accordance with the Medical Cannabis Act (MedCanG)
Advising and training cannabis companies inside and outside Europe
Communicating and coordinating with the competent 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
Solid knowledge of Good Manufacturing Practice (GMP) and regulatory requirements in the pharmaceutical industry
Strong sense of responsibility, analytical skills, and decisiveness
High level of initiative and ability to work independently
Excellent communication skills
Business-fluent German and English, both spoken and written
Permanent residence in Germany
Willingness to travel regularly within Germany
Willingness to travel occasionally worldwide (approx. 2–5 times per year)
Clean criminal record (does not need to be provided at the time of application)

Senior Consultant, Qualified Person

Key skills