Qualified person responsible for information and publicity
Local contact person for pharmacovigilance
Regulatory intelligence
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg
Job Summary
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg.
The role steers locally the quality, regulatory and compliance activities within the affiliate and in collaboration with EU departments in accordance with Belgian, Dutch and Luxembourg laws and regulations.
The position also fulfills the role of the Prevention advisor, provides ad hoc PMO, and endorses transversal activities carried out by various departments.
Matching Summary
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg.
Skills & Requirements
Must-have
Qualified Person Responsible for Information and Publicity
Local contact Person for Pharmacovigilance
Regulatory intelligence
Medical information management
Promotional and medical material review
Quality assurance / distribution / supply chain
Drug safety management
Nice-to-have
Collaborative Spirit
Bold Ingenuity
Driving Excellence
Patients First
Agile, strategic thinking
Cross-functional collaboration
Key Requirements
10 years pharmaceutical industry/biotech experience