Associate Director Pharmaceutical Affairs Benelux

beonemedicines.se

Not specified
Qualified person responsible for information and publicity (qp rip)
Local contact person for pharmacovigilance (lppv)
Belgium, netherlands, luxembourg regulatory knowledge
BeOne Medicines is seeking an Associate Director of Pharmaceutical Affairs for the Benelux region, responsible for regulatory compliance, medical information, and quality assurance in Belgium and Luxembourg. The ideal candidate should have a strong background in regulatory affairs within the pharmaceutical industry, preferably in oncology, and be fluent in English, French, or Dutch

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.
  • As Pharmaceutical affairs Associate Director, he (she) also 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.
  • He/she organizes a backing-up for the QP RIP role as applicable and fulfills the role of the Prevention advisor, provides ad hoc PMO, and endorses the transversal activities carried out by various departments.

Matching Summary

Match Score: 85

BeOne Medicines is seeking an Associate Director of Pharmaceutical Affairs for the Benelux region, responsible for regulatory compliance, medical information, and quality assurance in Belgium and Luxembourg. The ideal candidate should have a strong background in regulatory affairs within the pharmaceutical industry, preferably in oncology, and be fluent in English, French, or Dutch.

Skills & Requirements

Must-have

  • Qualified Person Responsible for Information and Publicity (QP RIP)
  • Local contact Person for Pharmacovigilance (LPPV)
  • Belgium, Netherlands, Luxembourg regulatory knowledge
  • Medical information management
  • Promotional and medical material review
  • Quality assurance and distribution oversight

Nice-to-have

  • Collaborative and passionate interest in fighting cancer
  • Experience in a dynamic, lean environment
  • Cross-functional collaboration and out-of-the-box thinking
  • Agile, strategic thinking

Key Requirements

  • Minimum of 10 years pharmaceutical industry/biotech experience
  • Regulatory affairs experience in Belgium
  • Certified Prevention Adviser Level III
  • Fluent in English, French or Dutch
  • Oncology market experience strongly preferred
  • PharmD or PhD, or Bachelor of Science, Master’s in Science or Business

Work Rights

Not specified

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