Back to jobs

Director, Strategy & Operations, Supply Chain / CMC

San Francisco, California, United States

About Eidos Therapeutics & BridgeBio Pharma

Eidos Therapeutics, an affiliate of BridgeBio Pharma, is a commercial stage biopharmaceutical company focused on addressing the large and growing unmet need in diseases caused by transthyretin, or TTR, amyloidosis, or ATTR. We seek to treat this well-defined family of diseases at their collective source by stabilizing TTR. Attruby (acoramdis) is an orally administered small molecule designed to stabilize TTR, a best-in-class treatment aiming to halt the progression of ATTR diseases.

BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We bridge the gap between remarkable advancements in genetic science in academic institutions and the delivery of meaningful medicines to patients. Founded in 2015, the company has built a portfolio of 30+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs. 

Our focus on scientific excellence and rapid execution aims to translate today’s discoveries into tomorrow’s medicines. We have U.S. offices in San Francisco, Palo Alto, and Raleigh, with small satellites in other parts of the country. We also have international offices in Montreal, Canada, and Zurich, Switzerland, and are expanding across Europe. 

To learn more about our story and company culture, visit us at eidostx.com/ | https://bridgebio.com

Who You Are

The Director, Supply Chain Strategy & Operations will join a lean team that enables the commercial supply of multiple products across the BridgeBio ecosystem of companies, with an immediate focus on the commercial supply of Attruby/Beyonttra, our recently FDA, EMA, and PMDA-approved product, and subsequent focus on other programs and geographies. This individual will ensure the support of an efficient, uninterrupted supply of medicine by developing strategies to improve our CMC/Supply Chain function, play an operational role in the implementation of new methods, and serve as a key interface between the CMC/Supply Chain team and partners across the business (e.g., Commercial, FP&A, Accounting, Legal, BD, Management). 

This is a primarily in-person role that requires in-office collaboration three times per week in our San Francisco or Palo Alto Offices 

Responsibilities

  • Work with the Commercial team to maintain an updated demand forecast, and integrate it into the supply forecast
  • Ensure alignment between the CMC/Supply team and other teams, including FP&A, Accounting, Legal, Business Development, Commercial Operations, the CFO, and the CEO of BridgeBio
  • Identify strategic investments that BridgeBio can make to its CMC processes/supply chain and model the risk-adjusted NPV to determine which should be pursued
  • Contribute to the ongoing development and maintenance of integrated cross-functional plans to enable accurate financial analysis, resource forecasting, and deadline management
  • Define and track key performance metrics for CMC/Supply Chain risk management, ensuring potential issues are identified early and proactively addressed through contingency planning and cross-functional coordination
  • Translate technical CMC/Supply Chain objectives into clear business deliverables/presentations to the Executive Team, functional heads, and other key stakeholders 

No matter your role at BridgeBio, successful team members are:

  • Patient Champions, who put patients first and uphold strict ethical standards
  • Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset
  • Truth Seekers, who are detailed, rational, and humble problem solvers
  • Individuals Who Inspire Excellence in themselves and those around them
  • High-quality executors, who execute against goals and milestones with quality, precision, and speed

Education, Experience & Skills Requirements

  • Passion for getting lifesaving medicines into the hands of patients quickly, efficiently, and compliantly 
  • Undergraduate or graduate degree focusing on the healthcare business/ life sciences industry. Master’s degree in chemistry/chemical engineering, MBA, or PhD preferred but not required 
  • Experience working on supply chain and CMC projects, including creating and monitoring key performance metrics, with direct biopharma expertise
  • 3-5+ years of experience in life sciences consulting/investment banking preferred 
  • Excellent project management skills and ability to handle multiple projects simultaneously 
  • Ability to work independently and as part of a team 
  • Must be comfortable with ambiguity 
  • Proactive problem solver
  • Fast (extremely fast) learner 
  • Strong communication skills 
  • Strong leadership skills and ability to influence functional stakeholders to set direction, align work efforts, and ensure outstanding execution
  • The ability to travel (up to 20% of the time) is required 

What We Offer

  • Patient Days, where we are fortunate to hear directly from individuals living with the conditions we are seeking to impact throughout the year and learn how we can improve our efforts
  • A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, and let the science speak
  • An unyielding commitment to always putting patients first. Learn more about how we do this here
  • A de-centralized model that enables our program teams to focus on advancing science and helping patients. Our affiliate structure is designed to eliminate bureaucracy and put decision-making power in the hands of those closest to the science
  • A place where you own the vision – both for your program and your own career path
  • A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game
  • Access to learning and development resources to help you get in the best professional shape of your life
  • Robust and market-competitive compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement programs)
  • Flexible PTO
  • Rapid career advancement for strong performers
  • Potential ability to work on multiple BridgeBio Pharma programs across multiple therapeutic areas over time 
  • Partnerships with leading institutions
  • Commitment to Diversity, Equity & Inclusion
At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.

Salary

$200,000 - $250,000 USD

Apply for this job

*

indicates a required field

Resume/CV*

Accepted file types: pdf, doc, docx, txt, rtf

Cover Letter

Accepted file types: pdf, doc, docx, txt, rtf


Select...
Select...
Select...

U.S. Standard Demographic Questions

We invite applicants to share their demographic background. If you choose to complete this survey, your responses may be used to identify areas of improvement in our hiring process.
Select...
Select...
Select...
Select...
Select...
Select...