Manager/Sr. Manager, Training and Doc Control Support Systems

Minimum 5-10 years of experience in a quality assurance role in the pharmaceutical industry required

Excellent knowledge and understanding of applicable GxP regulations

Familiarity with Microsoft Office Suite, Adobe Pro, etc.

Ready to embrace BridgeBio’s core values and diverse corporate culture

At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits.

As a global company, our comprehensive benefits may vary based on location.

Document Control & Training Manager will lead and manage Document Control activities for BridgeBio and its affiliates as well as perform training-related tasks to support the Training Program.

This individual will develop and implement document management processes as well as perform document administration tasks in Veeva QualityDocs, ensuring that documents are in compliance with GxPs and with Good Documentation Practices.

This individual will interact closely with internal stakeholders such as Quality Control, Manufacturing, Regulatory Affairs, Supply Chain, and Clinical.

Responsible for reviewing Document Change Controls to ensure proper revision control of records and closure

Execute user test scripts for the electronic document management system during changes to the systems

Manage Learner Roles, curriculums, and training requirements in the Learning Management System (Veeva Training)