Pharmacovigilance Manager

Job DescriptionWe are looking for an experienced Pharmacovigilance Manager for a permanent position in our Pharmacovigilance Unit in Espoo. About Your RoleYou operate as part of a multidisciplinary team of experts, and your tasks include SAE and ICSR reporting processes for molecules in development, authorised medicinal products and non-medical products, work outsourcing and the development and monitoring of internal and outsourced processes in accordance with Orion's guidelines, regulatory requirements, and cooperation agreements. In addition, you will participate in the drafting of agreements related to SAE processing.

Your work also includes international cooperation with various parties, answering inquiries and participating in the organisation of trainings. You take care of the quality and integrity of the collected information and actively participate in the development and maintenance of operating instructions. What We OfferWe offer a comfortable working environment as well as a versatile and challenging task where you can apply your knowledge and further develop your professionalism in the pharmaceutical industry. It is important for us Orionees to nurture mutual respect and appreciation for each other's work and views.

Listening to others and taking different perspectives into account are valuable qualities for us to achieve results together. We work with an uncompromising attitude to ensure Orion's future success. 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/ . Our expectationsSuccess In Your Role Requires You Toqualifications suited for the task, e. g. in pharmacy, biosciences or health careat least two years of experience in pharmacovigilance tasks; experience in SAE and spontaneous reporting and related process developmentfluent IT skills and knowledge of information systems, previous experience with pharmacovigilance systems is considered an advantage (e. g.

Rave, Argus, ARISg)initiative, readiness for change and enthusiasm precision, systematic working skills with several tasks running simultaneously in parallel and within strict time limitsability to manage entities and willingness to take responsibility for taking things forwardflexibility, solution focus and the ability to work independently, but also as a team memberIn addition, we require a good command of the English language (written and spoken). Communication and documentation takes place mainly in English, but success in the task also requires mastery of the Finnish language. How To Apply And Additional InformationWe process applications already during the application period.

If you are interested, please apply no later than Saturday August 16th, 2025. For more information about the assignment, please contact Head of PV Case Management Mila Harri, tel. +358 50 966 4288 (best available on Mon 11. 8. 9-10 and 16-17, Fri 15. 8. 8-9 and 15-16). Approved medical examination which also includes drug testing is required prior to the employment. We will also carry out a security clearance prior to the employment for the selected person. Unit DescriptionQuality management (QM) is responsible for ensuring the quality of materials, products and operations, as well as maintaining and developing the quality system and monitoring the regulatory environment.

Pharmacovigilance and Patient Safety unit is responsible for the global pharmacovigilance system of Orion Corporation and for the continuous safety surveillance, regulatory reporting and safety risk management activities of human and veterinary medicinal and non-medicinal products. The QM function consists of about 350 experts who work in Quality Control, Quality Assurance, Quality System, Method Development and the Pharmacovigilance & Drug safety unit. We are located in Espoo, Turku, Salo and Kuopio plants, in addition to the Quality Assurance team in India reporting dotted-line to QM.

Pharmacovigilance & Patient Safety unit is responsible for the safety monitoring, regulatory reporting and development of international pharmacovigilance activities for Orion's human and veterinary medicinal and non-medicinal products. About UsOrion Pharma is a globally operating Nordic pharmaceutical company – a builder of well-being for over a hundred years. We’re home to more than 4,000 Orionees around the world, and we’re proud to be known as a responsible employer and a great place to work. At Orion Pharma, people are truly valued and trusted, encouraged to grow, and supported by a culture where every voice is heard.

We appreciate each other, strive for excellence, and build the future. Together we develop, manufacture, and market human and veterinary pharmaceuticals and active pharmaceutical ingredients. Our extensive portfolio includes proprietary and generic medicines as well as consumer health products. The core therapy areas of our pharmaceutical R&D are oncology and pain. Proprietary products developed by Orion Pharma are used to treat cancer, neurological diseases, respiratory diseases, and more. We offer careers with a clear purpose: empowering people to live their lives to the fullest.