For the European HQ of a medical device company in Mechelen, we are urgently looking for a Complaint and Post Market Surveillance Manager EMEA. Do you have minimum 5 years of experience in quality systems, complaint, or post market surveillance within a medical device company? Do you like to take ownership and you are solution oriented?
Regulatory Affairs/Pharmacovigilance officer (id 1755)
For a global market leader in the field where medical devices meet pharmaceuticals, we are looking for a Quality Assurance Supervisor, working in the production site in Belgium.
For a for a leading pharmaceutical company, we are looking for a Medical Safety Assessment Manager for the worldwide Patient Safety Department. The function holder will lead all medical safety assessment and related activities for assigned molecules, in clinical research and already commercialized.