Karo Pharma delivers smart choices for everyday healthcare. We own and commercialize branded, original over-the-counter products and prescription medicines.
Our products are available in more than 60 countries, with Europe and the Nordic region as our core markets. Karo Pharma is headquartered in Stockholm, Sweden and listed on Nasdaq Stockholm Mid Cap.
Post Market Surveillance specialist
As a Post Market Surveillance specialist, you will have an important role in the company’s Medical Device and cosmetics portfolio management. This is an operational and strategic role, in which the you will have the opportunity to set processes and redefine existing processes.
In this role you will be responsible for coordinating, collecting and analyzing post-market surveillance data such as complaints data, in accordance with regulations. Furthermore, you will collaborate with cross-functional groups to ensure quality and regulatory requirements are met while working on complaints handling, medical device and vigilance reporting, potential recall situations, risk management activities and post-market surveillance reports.
To be successful in this application you should have a minimum of 4 years Regulatory Affairs experience in compliance to ISO 13485 and MDD/MDR.
For additional information about this new role at Karo Pharma, please contact Helena Marteus: 070-1652259.
Read more about Post Market Surveillance Specialist here!