Director, Regulatory Vault Operations

GSK

Poland
Base: pln 381,750 to pln 636,250 gross; bonus: eli...
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Expert level knowledge of veeva regulatory vault
Strong experience with gxp validation and inspection readiness
Deep knowledge of regulatory submission platforms like ectd
** GSK is seeking a Director of Regulatory Vault Operations in Poland to lead strategic initiatives in regulatory compliance and system optimization within their global organization. The ideal candidate will have extensive experience in regulatory affairs, particularly with Veeva Regulatory Vault, and a strong background in the pharmaceutical or life sciences industry. **

Job Summary

  • This role sets the strategic direction for GSK's Regulatory Vault capability to enable compliant and efficient decision-making globally.
  • The successful candidate will lead a geographically diverse team while ensuring zero findings during regular inspections and maintaining system reliability.
  • GSK offers a competitive annual base salary ranging from PLN 381,750 to PLN 636,250 gross along with comprehensive benefits including private healthcare and parental leave.

Matching Summary

Match Score: 75

** GSK is seeking a Director of Regulatory Vault Operations in Poland to lead strategic initiatives in regulatory compliance and system optimization within their global organization. The ideal candidate will have extensive experience in regulatory affairs, particularly with Veeva Regulatory Vault, and a strong background in the pharmaceutical or life sciences industry. **

Salary

Base: PLN 381,750 to PLN 636,250 gross; Bonus: Eligible based on non-discretionary criteria; Benefits: Private healthcare, additional paid days off, life insurance, pension plan, fully paid parental leave

Skills & Requirements

Must-have

  • Expert level knowledge of Veeva Regulatory Vault
  • Strong experience with GxP validation and inspection readiness
  • Deep knowledge of regulatory submission platforms like eCTD
  • Proven expertise in data reporting and analytics
  • Experience leading cross-functional teams in matrixed organizations

Nice-to-have

  • Hands-on experience with business intelligence tools like Power BI
  • Formal training in leadership or project management (MBA/PMP)
  • Doctoral or equivalent advanced qualification (PhD/PharmD/MD)

Key Requirements

  • Advanced degree in Regulatory Affairs, Pharmaceutical Sciences, or related field
  • Strong experience in pharmaceutical industry regulatory affairs or clinical development
  • Demonstrated experience managing GxP compliance and Quality Management Systems

Work Rights

Not specified

Tailored Resume

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