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BridgeBio

Associate Director/Director Pharmaceutical Development

RemoteUnited States only
Published
Experience
Lead
Employment
Full-time
$223k–$239k/yr
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Open to US only. Set where you work from to check your eligibility.

No BS summary

PhD or advanced-degree pharmaceutical development leader with 7+ years in bio/pharma formulation development and clinical supply. Must understand CMC regulatory requirements for US/EU, CRO/CDMO manufacturing, clinical trial manufacturing, and pediatric formulations. Remote US role with 30% travel.

What you'll do

  • Provide strategic pharmaceutical development guidance as the CMC lead to cross-functional project teams.
  • Develop robust formulations and manufacturing processes to support development and rapid registration of QED products.
  • Review development and manufacturing programs at CROs/external vendors to ensure compliance with agreed proposals, quality standards, and timelines.
  • Review external data.
  • Manage drug forecasts and associated transactions.
  • Integrate and liaise effectively with the CMC team.
  • Provide formulation and clinical supply expertise/support in the preparation of regulatory submissions such as IB, IND, and NDA.
  • Develop complex formulation for pediatric indications.
  • Work effectively with CDMOs.

What they require

  • Ability to work effectively and collaboratively on cross-functional project teams in a fast-paced, dynamic environment under tight timelines.
  • 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 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.
  • PhD or advanced degree in Chemistry or Pharmacy with 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 CROs.
  • In-depth knowledge and understanding of CMC regulatory requirements for US and EU are required.
  • 30% travel expected.

Benefits

  • Annual performance bonus.
  • Company equity.
  • Generous health benefits.
  • Market-leading compensation.
  • 401(k) with employer match.
  • Employee Stock Purchase Program (ESPP).
  • Pre-tax commuter benefits for 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 employees and dependents.
  • Health Savings Account (HSA) with annual employer contributions.
  • Flexible Spending Accounts (FSA).
  • Fertility and family-forming benefits.
  • Expanded mental health support including therapy and coaching resources.
  • Hybrid work model with flexibility.
  • Flexible, take-what-you-need paid time off.
  • Company-paid holidays.
  • Comprehensive paid medical and parental leave.
  • Opportunities for skill development and internal mobility.
  • Career pathing through regular feedback.
  • Continuous education and professional development programs via LinkedIn Learning, LifeLabs, and BetterUp Coaching.
  • Financial rewards, peer-to-peer recognition, and growth opportunities for strong performance.

BridgeBio develops life-changing medicines for patients with unmet needs, focusing on rare disease and biopharma innovation.

BiotechMid-sizebridgebio.com/

Details

Apply routeGreenhouse
$223k–$239k/yr