Director, Regulatory Vault Operations

GSK

Poland
Base: pln 381,750 to pln 636,250 gross; bonus/equi...
Not specified (assumed office-based as location is in poland)
Expert knowledge of veeva regulatory vault
Gxp validation and inspection readiness experience
Enterprise service management and change control
GSK is seeking a Director of Regulatory Vault Operations in Poland to lead the strategic direction and enhance the efficiency of their regulatory systems. The role requires extensive experience in pharmaceutical regulatory affairs, particularly with Veeva Regulatory Vault, and strong leadership skills to manage cross-functional teams

Job Summary

  • This role sets the strategic direction for GSK's global Regulatory Vault capability to enable compliant and efficient decision-making.
  • The successful candidate will lead a geographically diverse team while ensuring zero findings during regular regulatory inspections.
  • The position offers a competitive salary range in Poland along with benefits including private healthcare and fully paid parental leave.

Matching Summary

Match Score: 85

GSK is seeking a Director of Regulatory Vault Operations in Poland to lead the strategic direction and enhance the efficiency of their regulatory systems. The role requires extensive experience in pharmaceutical regulatory affairs, particularly with Veeva Regulatory Vault, and strong leadership skills to manage cross-functional teams.

Salary

Base: PLN 381,750 to PLN 636,250 gross; Bonus/Equity: Eligible for non-discretionary bonus and performance awards; Benefits: Private healthcare, additional paid days off, life insurance, pension plan, and parental leave

Skills & Requirements

Must-have

  • Expert knowledge of Veeva Regulatory Vault
  • GxP validation and inspection readiness experience
  • Enterprise service management and change control
  • Global regulatory compliance and risk management
  • Leading cross-functional matrixed teams

Nice-to-have

  • Experience with Power BI or visualization tools
  • Doctoral degree in life sciences or business
  • Formal project management certification like PMP
  • Hands-on configuration customization of Vault platform

Key Requirements

  • Advanced degree in Regulatory Affairs or related field
  • Strong experience in pharmaceutical industry regulatory operations
  • Deep knowledge of RIM, eCTD, and submission environments

Work Rights

Not specified

Tailored Resume

Cover Letter