.We're looking for people who are determined to make life better for people around the world.Interested? Then become part of our team and start as soon as possible as:Deputy European Union (EU) Qualified Person for Pharmacovigilance (m / f / d) What challenges await you?Deputise for the European Union QPPV as required and according to delegation and specifically to fulfil the legal and regulatory requirements for the QPPV role in his or her absence.Provide strategic and technical pharmacovigilance advice to Global Patient Safety (GPS), and other regulatory and medical functions within the Medicines Development Unit.Play an active role in the GPS Leadership Team, Safety Review Committee (SRC) and other committees as required.Provide training, coaching, and mentoring, demonstrating Global Patient Safety expertise and leadership.Deputise for the EU QPPV on the Global Product Labelling Committee (GPLC) as required.Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.Fulfil the legal and regulatory requirements for the EU Qualified Person responsible for pharmacovigilance role as defined by prevailing European legislation and guidelines in the absence of the EU QPPV or as delegated by the EU QPPV.Ensure appropriate cover with the QPPV including provision of all the necessary information to fulfil the role.Maintain current awareness of the evolving EU regulatory environment, provide timely feedback to GPS leadership, and provide advice to the Medicines Quality Organisation as appropriate.Review and provide expert input to EU regulatory submissions PASS protocols and actions taken in response to emerging safety concerns in order to ensure appropriate risk minimisation and the timeliness, correctness and completeness of all pharmacovigilance data submitted to the Competent Authorities and to the European Medicines Agency (EMA).Provide QPPV input to GPLC in the absence of the QPPV or as delegated.Fulfill all other QPPV obligations as stipulated in the Good Vigilance Practice (GVP) guidelines as delegated by the QPPV.Provide an independent expert viewpoint on specific safety issues.Maintain links with Global Regulatory Affairs and provide technical consultancy to safety sections of European regulatory submissions, responses to Committee for Medicinal Products for Human Use (CHMP) / other European regulatory authority safety questions, and guidance on safety sections of Summary of Product Characteristics, etc.Provide technical leadership through active external involvement in pharmacovigilance forums and bring shared learning back into the Lilly organization
