BridgeBio

1 month ago

Sr Project Manager

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 3 hours agoStatus: Live

Job Summary

Senior Manager, Project Management supporting the CMC team to ensure cross-functional planning is integrated into department activities, with identified risks and mitigation plans, proactive resource planning, and effective communication with internal stakeholders and external partners. Responsible for coordinating CMC/QA activities, managing CDMOs to align with timelines, contributing to long-range planning and budgeting, and supporting regulatory filings in a hybrid San Francisco setting.

Location: San Francisco

Workplace: Hybrid

Employment Type: Full time

Job Function: Program & Project Management (PMO)

Seniority: Manager level

Key Responsibilities

•Organize and coordinate CMC/QA team activities and deliverables; manage weekly team meetings; prepare agendas and keep track of action items
•Interface and manage multiple CDMOs to drive manufacturing activities in alignment with CMC timelines and clinical and commercial supply needs
•Coordinate drafting of certain sections of regulatory filing and cross-functional reviews. Organize document QC processes to ensure accuracy of content
•Contribute to long-range planning and budgetary planning. Work with Legal and Finance departments to drive and manage vendor contracts and purchase orders
•Effectively manage multiple responsibilities and deliverables concurrently

Travel: Low travel

Pay and Benefits

Salary: USD 160,000 - 175,000 annually

Perks:Health InsuranceDentalVisionHsaFsaPaid LeaveParental LeaveLife InsuranceCommuter BenefitsHybrid WorkRemote Work

Key Requirements

•M.S. or B.S. in chemistry, chemical engineering or equivalent preferred. Demonstrated understanding of science behind drug development is required
•A minimum of 10 years of biotech/pharma industry project management
•Track record of delivering in a fast-paced, innovative, dynamic environment while remaining flexible, proactive, resourceful, and efficient
•Expert planning and tracking skills, able to see the big picture, well‑organized, focused on results, capable of managing multiple projects, excellent time management concerning priorities and self‑management
•Ability to work strategically and independently with internal and external groups on multiple projects

Experience:10+ yearsBiotechPharmaBiopharma

Education:Bachelor's

Skills:CommunicationCross-functional collaborationTime managementStrategic thinkingProblem-solving

Languages:English

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

Website LinkedIn

Loading job details...

Preparing the role view and application actions.

BridgeBio

1 month ago

Sr Project Manager

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 3 hours agoStatus: Live

Job Summary

Location: San Francisco

Workplace: Hybrid

Employment Type: Full time

Job Function: Program & Project Management (PMO)

Seniority: Manager level

Key Responsibilities

•Organize and coordinate CMC/QA team activities and deliverables; manage weekly team meetings; prepare agendas and keep track of action items
•Interface and manage multiple CDMOs to drive manufacturing activities in alignment with CMC timelines and clinical and commercial supply needs
•Coordinate drafting of certain sections of regulatory filing and cross-functional reviews. Organize document QC processes to ensure accuracy of content
•Contribute to long-range planning and budgetary planning. Work with Legal and Finance departments to drive and manage vendor contracts and purchase orders
•Effectively manage multiple responsibilities and deliverables concurrently

Travel: Low travel

Pay and Benefits

Salary: USD 160,000 - 175,000 annually

Perks:Health InsuranceDentalVisionHsaFsaPaid LeaveParental LeaveLife InsuranceCommuter BenefitsHybrid WorkRemote Work

Key Requirements

•M.S. or B.S. in chemistry, chemical engineering or equivalent preferred. Demonstrated understanding of science behind drug development is required
•A minimum of 10 years of biotech/pharma industry project management
•Track record of delivering in a fast-paced, innovative, dynamic environment while remaining flexible, proactive, resourceful, and efficient
•Expert planning and tracking skills, able to see the big picture, well‑organized, focused on results, capable of managing multiple projects, excellent time management concerning priorities and self‑management
•Ability to work strategically and independently with internal and external groups on multiple projects

Experience:10+ yearsBiotechPharmaBiopharma

Education:Bachelor's

Skills:CommunicationCross-functional collaborationTime managementStrategic thinkingProblem-solving

Languages:English

Company Brief

BridgeBio

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

Website LinkedIn