Global Regulatory Documentation Manager

Bristol-Myers Squibb; Poland; Hybrid; PLN 206,000 - 249,000; Full time

Job summary

Bristol Myers Squibb in Warsaw is seeking a Manager, Global Scientific and Regulatory Documentation to lead the authoring of regulatory documents and coordinate cross-functional inputs for submissions across markets. The role supports development, submission, approval, and lifecycle management of products in the BMS pipeline.

The position requires 2–4 years in regulatory documentation, strong writing and organizational skills, and a hybrid work model with at least 50% onsite attendance at the

Qualifications

• Strong writing skills in authoring regulatory documents (IB, CSR, safety reports) and coordinating cross-functional input.
• Experience with regulatory documentation for global submissions.
• Ability to analyze complex scientific data and ensure quality and timeliness.

Responsibilities

• Coordinate and author regulatory documents for submissions and approvals across markets.
• Use advanced document tools to enhance efficiency, quality, and speed.
• Plan and manage timelines for all components of assigned documents.
• Participate in document strategy sessions and ensure messaging consistency.
• Review and edit documents to ensure accuracy and compliance.

Skills

Regulatory writing

Cross-functional collaboration

Complex data interpretation

Timeline management

Education

PharmD/PhD in a relevant scientific discipline or Master's/Bachelor's degree

Tools

Document management system

Document publishing process

Job description

Bristol Myers Squibb in Warsaw is seeking a Manager, Global Scientific and Regulatory Documentation to lead the authoring of regulatory documents and coordinate cross-functional inputs for submissions across markets. The role supports development, submission, approval, and lifecycle management of products in the BMS pipeline.

The position requires 2–4 years in regulatory documentation, strong writing and organizational skills, and a hybrid work model with at least 50% onsite attendance at the