Note: The job is a remote job and is open to candidates in USA. BridgeBio is a pioneering company in the biotech industry focused on developing life-changing medicines for patients with unmet needs. The Associate Director/Director of Pharmaceutical Development will provide strategic guidance as the CMC lead to cross-functional project teams and develop robust formulations and manufacturing processes to support product development.
Responsibilities
• Ability to work effectively and collaboratively on cross functional project teams, in a fast-paced, dynamic environment under tight timelines
• Develop complex formulation for pediatric indications
• Work effectively with CDMO's
• A team player, functional leader, effective listener, clear communicator and quick learner
• Clear, concise communication style with ability to interact internally and externally
• Willing to 'roll up his/her sleeves and do what it takes' to achieve critical program deliverables
• Hands-on experience in clinical trials management/study conduct, formulation development and clinical trial manufacturing
• Knowledge of commercial manufacture
Skills
• PhD or advanced degree in Chemistry or Pharmacy
• 7+ years of bio/pharmaceutical industry experience in formulation development and Clinical Supply
• Expertise in formulation in addition to knowledge of PK/PD principles, ADME concepts, and regulatory documentation and authorship
• Knowledge of import/export sensitivities
• Demonstrated ability to manage Clinical Supply, Formulation development and manufacture at CRO's
• In-depth knowledge and understanding of CMC Regulatory requirements for US and EU
• Ability to work effectively and collaboratively on cross functional project teams, in a fast-paced, dynamic environment under tight timelines
• Develop complex formulation for pediatric indications
• Work effectively with CDMO's
• A team player, functional leader, effective listener, clear communicator and quick learner
• Clear, concise communication style with ability to interact internally and externally
• Willing to “roll up his/her sleeves and do what it takes” to achieve critical program deliverables
• Hands-on experience in clinical trials management/study conduct, formulation development and clinical trial manufacturing
• Knowledge of commercial manufacture
Benefits
• 401(k) with employer match
• Employee Stock Purchase Program (ESPP)
• Pre-tax commuter benefits (transit and parking)
• Referral bonus for hired candidates
• Subsidized lunch and parking on in-office days
• 100% employer-paid medical, dental, and vision premiums for you and your dependents
• Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA)
• Fertility & family-forming benefits
• Expanded mental health support (therapy and coaching resources)
• Hybrid work model with flexibility
• Flexible, “take-what-you-need” paid time off and company-paid holidays
• Comprehensive paid medical and parental leave to care for yourself and your family
• People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility
• We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
• We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities
Company Overview
• BridgeBio focuses on the development and commercialization of precision medicines for various genetic diseases and cancers. It was founded in 2015, and is headquartered in Palo Alto, California, USA, with a workforce of 501-1000 employees. Its website is http://bridgebio.com.
Company H1B Sponsorship
• BridgeBio has a track record of offering H1B sponsorships, with 3 in 2026, 3 in 2025, 5 in 2024, 4 in 2023, 4 in 2022, 1 in 2021, 2 in 2020. Please note that this does not guarantee sponsorship for this specific role.