Pharmacovigilance Compliance And Oversight Manager

GALDERMA AUSTRALIA

Base: $130,000-$180,000; bonus/equity: annual shor...
Hybrid
Pv quality management system maintenance
Deviation and capa management expertise
Regulatory inspection readiness support
Galderma Australia is seeking a Pharmacovigilance Compliance and Oversight Manager to oversee the quality management system for pharmacovigilance, ensuring compliance with relevant regulations and company policies. The ideal candidate should have advanced qualifications in life sciences, extensive experience in pharmacovigilance quality and compliance, and strong analytical and communication skills

Job Summary

  • The role is responsible for overseeing and maintaining the local PV quality management system to ensure compliance with U.S. and global regulations.
  • Candidates must possess an advanced degree in life sciences or pharmacy along with at least six years of experience in pharmacovigilance quality or compliance.
  • The position offers a competitive base salary range of $130,000 to $180,000 plus annual short-term incentive opportunities and comprehensive benefits.

Matching Summary

Match Score: 85

Galderma Australia is seeking a Pharmacovigilance Compliance and Oversight Manager to oversee the quality management system for pharmacovigilance, ensuring compliance with relevant regulations and company policies. The ideal candidate should have advanced qualifications in life sciences, extensive experience in pharmacovigilance quality and compliance, and strong analytical and communication skills.

Salary

Base: $130,000-$180,000; Bonus/Equity: Annual short-term incentive program based on corporate and individual performance; Benefits: Health insurance, 401(k) match, generous PTO, hybrid work schedules

Skills & Requirements

Must-have

  • PV quality management system maintenance
  • Deviation and CAPA management expertise
  • Regulatory inspection readiness support
  • FDA and ICH pharmacovigilance regulations knowledge
  • Root cause analysis and risk evaluation

Nice-to-have

  • Matrix environment collaboration skills
  • Continuous improvement initiative mindset
  • Strong presentation of compliance metrics
  • Cross-functional stakeholder partnership

Key Requirements

  • Master's, PharmD, MD, or PhD in life sciences required
  • 6+ years experience in pharmaceutical/biotech PV quality
  • In-depth knowledge of FDA requirements and GVP modules

Work Rights

Not specified

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