Document Control & Training Leader — Biopharma QA

BridgeBio; San Francisco (CA); Hybrid; USD 135,700 - 185,000; Full time

Benefits offered by this job

Hybrid work model

Employee Stock Purchase Program (ESPP)

401(k) with employer match

Subsidized lunch and parking

Flexible paid time off

Company-paid health premiums

Job summary

BridgeBio in San Francisco seeks a seasoned Document Control & Training Manager to lead our document control program and training initiatives across the organization. You will manage Veeva QualityDocs, drive revision control, and support regulatory inspections with cross‑functional teams in Quality, Manufacturing, Regulatory Affairs, and Supply Chain.

You have 5–10 years in pharmaceutical QA, strong GxP knowledge, and hands‑on experience with EDMS and LMS systems (Veeva).

Qualifications

• Bachelor’s degree or higher in a relevant field.
• 5–10 years of experience in a quality assurance role in the pharmaceutical industry.
• Experience with EDMS and LMS systems, preferably Veeva Quality Docs and Veeva Training.
• Excellent knowledge and understanding of applicable GxP regulations.
• Experience in identification and resolution of Good Documentation Practices issues.
• Proficiency with Microsoft Office Suite and document management tooling.

Responsibilities

• Lead Document Control compliance and process improvement efforts.
• Plan, coordinate, and manage document control activities and processes.
• Format, issue, and maintain documents for training with accurate revision control.
• Review Document Change Controls to ensure proper records closure.
• Oversee periodic document reviews and coordinate with stakeholders.
• Perform Business Administrator duties in the EDM system (Veeva QualityDocs).
• Execute user test scripts for the EDM system during changes.
• Manage Learner Roles, curriculums, and training needs in Veeva Training.
• Support onsite audits and regulatory inspections.
• Tackle projects to improve quality systems as assigned.

Skills

Document Control

Training Management

Quality Assurance

GxP Knowledge

EDMS

LMS

Veeva QualityDocs

Veeva Training

Microsoft Office

Communication

Education

Bachelor’s degree or higher

Tools

Veeva QualityDocs

Veeva Training

LMS

Job description

BridgeBio in San Francisco seeks a seasoned Document Control & Training Manager to lead our document control program and training initiatives across the organization. You will manage Veeva QualityDocs, drive revision control, and support regulatory inspections with cross‑functional teams in Quality, Manufacturing, Regulatory Affairs, and Supply Chain.

You have 5–10 years in pharmaceutical QA, strong GxP knowledge, and hands‑on experience with EDMS and LMS systems (Veeva).