Your profile
\nAt least 5 years of hands-on experience in quality assurance, with a demonstrated ability to manage quality operations for injectable pharmaceuticals in the EU.
Experience of short-shelf or point of care products (e.g. radiopharmaceuticals or ATMPs) is an advantage.
In-depth knowledge of GMP and relevant pharmaceutical regulations in the EU with experience of FDA an advantage. A broader knowledge of GLP and medical devices is desirable, but not essential.
Demonstrated experience in the development and continuous improvement of cGxP quality systems.
Experience in the set-up and management of third-party vendors and suppliers.
Excellent problem-solving, analytical, and communication skills.
Innovation mindset: comfortable in a startup environment where proactivity, agility, and innovation are prized.
Familiarity with electronic Quality Management Systems (eQMS) and Application Lifecycle Management (ALM) for contracting, integration, and operational management.
Working in an international, interdisciplinary, and cross-functional team: experience collaborating with a diverse group of strong scientific and development experts.
Fluent in English and German