You will be part of a small team of experienced pharmacovigilance (PV) experts, with each member holding similar responsibilities within the QPPV office. For senior experts, there is also the possibility to step into a team leader role. In this position, you will collaborate closely with the QPPV, global PV unit management, subject matter experts, R&D QA (PV auditors), as well as global affiliates and service providers.
Your responsibilities cover various aspects of maintaining and developing the pharmacovigilance system globally at the company's headquarters PV unit. Weekly duties include:
Managing pharmacovigilance agreements (with licensing partners and service providers) and due diligence activities
Organizing pharmacovigilance training
Overseeing inspections and audit-related work when the pharmacovigilance system is evaluated by authorities or business partners
Supervising affiliate and service provider PV activities
Maintaining the Pharmacovigilance System Master File
Coordinating and developing pharmacovigilance business continuity processes
What you can expect from us
At Orion, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life.
Please visit our website to find further information about our values and Orion as an employer https://www.orion.fi/en/careers/orion-as-an-employer/.
What are we looking for?
We are seeking a senior expert with a minimum of five years' previous experience in pharmacovigilance activities. The ideal candidate possesses strong cross-functional collaboration a