DESCRIPTION OF POSITION

Your main responsibilities will include

• coordination and preparation of periodic safety review documents for human and veterinary products
• safety monitoring and signal management related activities
• preparation and maintenance of Risk Management Plans
• coordination and monitoring global implementation of risk minimisation materials
• activities related to safety variation process
• post-market surveillance and vigilance tasks related to medical devices and non-medicinal products

DESCRIPTION OF UNIT

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.

REQUIREMENTS

• Master’s degree in Pharmacy or Life Sciences
• At least 3 years of experience in Pharmacovigilance
• Strong organizational skills and the ability to manage multiple priorities effectively
• Fluent both in Finnish and English
  We wish that you also have positive attitude, good team working skills and the ability to operate cross-functionally as well as independently.

#LI-ORION

Orion Corporation operates in more than 30 countries, where we Orionees, 3600 in total, work in all kinds of positions. Among us there are Research Scientists, Laboratory Technicians, Engineers and IT Specialists as well as people working in Production, just to mention some examples. We offer diverse and responsible jobs to our personnel in a truly multi-disciplinary work environment. We encourage people to develop their competences and offer opportunities to affect the job description and creating their own career path at Orion. We are searching for top talents who are ready to share our passion for the work that we do

• coordination and preparation of periodic safety review documents for human and veterinary products
• safety monitoring and signal management related activities
• preparation and maintenance of Risk Management Plans
• coordination and monitoring global implementation of risk minimisation materials
• activities related to safety variation process
• post-market surveillance and vigilance tasks related to medical devices and non-medicinal product