Constant and systematic monitoring of the safety of medicinal products (pharmacovigilance) is one of the marketing authorisation holder's key tasks. During your internship, you will be directly involved in the team from the beginning.
In the "Product Defects" team, you will provide support, among other things, in the categorisation, medical assessment and identification of measures for complaints and deviations as part of stability studies ("out of specification"). On top of that, you will constantly be in close contact with numerous other departments such as Quality Assurance and Quality Control, as well as with pharmacies and authorities.
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In the "Quality Management" team, you will deal with processes of the Pharmacovigilance Department, design, optimise and map them in Working Instructions. You will additionally provide support in the preparation and follow-up of audits and training sessions. Implementing regulatory and internal/global stipulations as part of pharmacovigilance quality management rounds off your assignment.
