Associate Director/Director Pharmaceutical Development
About The Position
In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work.
Requirements
- 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 CRO’s.
- In-depth knowledge and understanding of CMC Regulatory requirements for US and EU are required
Responsibilities
- 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 CRO’s/external vendors to ensure compliance with agreed proposals, quality standards and timelines. Review external data.
- Manage drug forecasts and any associated transactions
- Integrate and liaise effectively with CMC team
- Provide formulation and Clinical supply expertise/support in the preparation of regulatory submissions (e.g. IB, IND, NDA).
- 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
- Market-leading compensation
- 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
- Career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
Ph.D. or professional degree
