Training & Document Control Manager, GxP QA

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

Benefits offered by this job

Market-leading compensation

401(k) with employer match

Employee Stock Purchase Program (ESPP)

Pre-tax commuter benefits

Referral bonus

Subsidized lunch and parking

100% employer-paid medical, dental, &

Job summary

BridgeBio Pharma in San Francisco is seeking a Manager/Sr. Manager, Training and Doc Control Support Systems to lead document control for BridgeBio and affiliates and to support training programs through Veeva systems.

The role requires a Bachelor’s degree and 5–10 years of QA experience in pharma, with strong GxP knowledge and EDMS/LMS expertise. Hybrid in-office collaboration 2–3x weekly in SF, contributing to quality improvements across departments.

Qualifications

• Bachelor’s degree or higher.
• 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.

Responsibilities

• Lead Document Control compliance and process improvement efforts
• Manage, plan, and coordinate document control activities and processes
• Manage documentation by processing, formatting, issuing the documents for training, and making it effective accurately
• Responsible for reviewing Document Change Controls to ensure proper revision control of records and closure
• Manage document periodic review process and coordinate with the stakeholders on its completion
• Perform Business Administrator activities in the electronic document management system (Veeva QualityDocs)
• 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)
• Support onsite audit/ and or in any regulatory inspections
• Perform other projects related to improvement of quality systems as needed and required by management
• Other duties as assigned

Skills

Quality assurance

Technical writing

Communication

Attention to detail

Team collaboration

Education

Bachelor’s degree

Tools

Veeva QualityDocs

Veeva Training

Microsoft Office

Adobe Pro

Job description

BridgeBio Pharma in San Francisco is seeking a Manager/Sr. Manager, Training and Doc Control Support Systems to lead document control for BridgeBio and affiliates and to support training programs through Veeva systems.

The role requires a Bachelor’s degree and 5–10 years of QA experience in pharma, with strong GxP knowledge and EDMS/LMS expertise. Hybrid in-office collaboration 2–3x weekly in SF, contributing to quality improvements across departments.