Base: pln 381,750 to pln 636,250 gross; bonus/equi...
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Expert level veeva regulatory vault knowledge
Gxp validation and inspection readiness experience
Global regulatory affairs and compliance management
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GSK is seeking a Director of Regulatory Vault Operations to lead and optimize regulatory systems and processes within their global organization. The ideal candidate will have extensive experience in regulatory affairs, GxP validation, and cross-functional collaboration in the pharmaceutical industry.
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Job Summary
This role sits at the intersection of regulatory science, data, digital, and operations to enable compliant decision-making at scale.
The successful candidate will lead a geographically diverse team to ensure system reliability, zero defects, and excellent end-user experiences.
The position 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
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GSK is seeking a Director of Regulatory Vault Operations to lead and optimize regulatory systems and processes within their global organization. The ideal candidate will have extensive experience in regulatory affairs, GxP validation, and cross-functional collaboration in the pharmaceutical industry.
**
Salary
Base: PLN 381,750 to PLN 636,250 gross; Bonus/Equity: Eligible for bonus based on criteria; Benefits: Private healthcare, additional paid days off, life insurance, pension plan, fully paid parental leave
Skills & Requirements
Must-have
Expert level Veeva Regulatory Vault knowledge
GxP validation and inspection readiness experience
Global regulatory affairs and compliance management
Enterprise service management and change control
Leading cross-functional matrixed organizations
Nice-to-have
Hands-on business intelligence and visualization tools
Formal leadership or project management training
Doctoral degree in relevant scientific discipline
Experience with Power BI or similar analytics
Advanced MBA or PMP certification
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