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Denk Pharma GmbH & Co. KG

Pharmacovigilance Manager

1w

Denk Pharma GmbH & Co. KG

Munich, DE · Full-time · €70,000 – €95,000

About this role

DENK PHARMA has been a family-owned company active in over 80 countries since 1948. Under the slogan 'Quality for your Health – Made in Germany', we provide customers worldwide with the same medicines and supplements available in Germany, produced and quality-controlled nearly 100% in Germany.

As Pharmacovigilance Manager, you ensure worldwide patient safety for our products. You continuously develop the global pharmacovigilance system and independently manage essential PV processes. Proactive risk management and structured work secure high quality standards for international market success.

Handle PV system development by maintaining databases and creating documents like PSURs, RMPs, PV contracts, and SOPs. Perform scientific evaluation of literature cases and spontaneous reports, such as adverse event notifications. Plan risk-minimizing measures including educational materials.

Prepare for PV audits and authority inspections while conducting trainings for global partners and employees. Collaborate interdisciplinary with internal departments and international partners to achieve PV goals. Strengthen patient safety awareness worldwide through knowledge transfer.

Requirements

  • Completed university degree with natural sciences focus, preferably human medicine or pharmacy
  • At least 2 years professional experience in pharmacovigilance
  • Familiarity with building PV systems and handling PV databases
  • Independent and structured working style
  • Reliable, highly engaged, and precise to meet pharmacovigilance quality requirements
  • Strong communicator and team player
  • Fluent in German and English

Responsibilities

  • Develop and maintain the global pharmacovigilance system and PV databases to ensure highest quality standards
  • Create, plan, and maintain essential PV documents including PSURs, RMPs, PV contracts, and SOPs for compliance
  • Conduct scientific evaluation and processing of literature cases and spontaneous reports like adverse events
  • Plan and implement risk-minimizing measures such as educational materials to promote safe product use
  • Prepare for and support PV audits and authority inspections
  • Plan and deliver PV trainings for worldwide partners and employees to strengthen patient safety awareness
  • Collaborate with internal departments and international partners to achieve PV goals