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

BridgeBio
San Francisco
Workplace: HybridFull timeUSD 135,700 - 175,000 annuallyFunction: Education & TrainingExperience: 5-10 yearsEducation: bachelorsSkills: ["Attention to detail","Communication","Organizational skills","Teamwork","Writing"]

Lead document control and training activities for BridgeBio and affiliates, developing and implementing document management processes in Veeva QualityDocs, ensuring GxP compliance and Good Documentation Practices. Oversee training tasks in Veeva Training, coordinate with Quality Control, Manufacturing, Regulatory Affairs, Supply Chain, and Clinical in a hybrid San Francisco setting, driving process improvements and regulatory readiness.

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BridgeBio
BridgeBio
2 months ago

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

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Source: Company careers pageValidated by: Fursa AI
Last checked: 5 hours agoStatus: Live

Job Summary

Lead document control and training activities for BridgeBio and affiliates, developing and implementing document management processes in Veeva QualityDocs, ensuring GxP compliance and Good Documentation Practices. Oversee training tasks in Veeva Training, coordinate with Quality Control, Manufacturing, Regulatory Affairs, Supply Chain, and Clinical in a hybrid San Francisco setting, driving process improvements and regulatory readiness.
Location: San Francisco
Workplace: Hybrid
Employment Type: Full time
Job Function: Education & Training
Seniority: Sr. Manager level

Key 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.

Pay and Benefits

Salary: USD 135,700 - 175,000 annually
Perks:Health Insurance401kHybrid Work

Key Requirements

  • •Bachelor’s degree or higher.
  • •Minimum 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 the identification and resolution of Good Documentation Practices issues.
Experience:5-10 yearsPharmaceuticalsBiopharma
Education:Bachelor's
Skills:Attention to detailCommunicationOrganizational skillsTeamworkWriting
Languages:English
Tech Stack:Veeva QualityDocsVeeva TrainingGxPEDMSLMSMicrosoft OfficeAdobe Pro

Company Brief

BridgeBio
Develops medicines for patients with genetic diseases by advancing targeted therapeutics from discovery through clinical development and commercialization, focusing on genetically defined diseases with high unmet medical need.
Industry: Biotech
Company Size: Large (251 to 1,000 employees)
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: Palo Alto, United States
Founded: 2015
WebsiteLinkedIn