Qualified person responsible for information and publicity (qp rip)
Local contact person for pharmacovigilance (lppv)
Regulatory intelligence and compliance
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.
Responsibilities include regulatory affairs, medical information management, promotional and medical material review, quality assurance, drug safety management, and prevention advisor role.
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 (QP RIP)
Local contact Person for Pharmacovigilance (LPPV)
Regulatory intelligence and compliance
Medical information management
Promotional and medical material review
Drug safety management
Compliance with Belgian, Dutch, Luxembourg laws
Nice-to-have
Scientific and business professionals
Collaborative and passionate interest
Dynamic, lean environment experience
Cross-functional collaboration
Out-of-the-box thinking
Agile, strategic thinking
Key Requirements
Minimum of 10 years pharmaceutical industry/biotech experience