YOUR CONTRIBUTION
Join our Pharmacovigilance Group within Global Product Safety and grow with new challenges. Your scope of work with us will include the following tasks:
- Maintaining and shaping the international pharmacovigilance (PV) system for all drugs of Merz Therapeutics including Merz Entities, license/distribution partners and service providers of Merz Therapeutics focusing on maintaining information channels, responsibilities, and work processes in collaboration with the QPPV and the German "Stufenplanbeauftragte".
- Maintaining and updating the Pharmacovigilance System Master File (EEA/UK-PSMF)
- Organizing and performing internal and external pharmacovigilance trainings
- Creation and updating of local and global PV operating procedures and work instructions (SOPs, WIs)
- Creating and updating Safety Agreements for the exchange of safety-related information with Merz affiliates, as well as licensing and distribution partners worldwide
- Commissioning and supervision of vigilance service providers for outsourced vigilance activities as well as preparation and updating of the corresponding contracts
- Monitoring of risk and referral procedures and coordination of the resulting measures, e.g. recalls / risk defense, in alignment with responsible functions
- Active preparation and follow-up of PV audits and PV inspections and to ensure the implementation of resulting Corrective and Preventive Actions