Senior Director, Commercial Manufacturing & CMC Development San Francisco, CA/Hybrid
Company: BridgeBio Pharma
Location: Palo Alto
Posted on: February 2, 2025
Job Description:
Eidos Therapeutics, an affiliate of BridgeBio Pharma, is a Phase
3 developmental-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. Our investigational product, acoramidis (AG10), is
an orally administered small molecule designed to potently
stabilize TTR, a potentially 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.We are seeking a seasoned
pharmaceutical leader to guide commercial manufacturing operations
and CMC development across all stages of drug substance (DS) and
drug product (DP) supply. This individual will leverage a deep
background in small-molecule drug discovery, process development,
and large-scale commercial manufacturing to ensure reliable product
quality, regulatory compliance, and on-time global
supply.Responsibilities
- Commercial Manufacturing Leadership:
- Oversee end-to-end commercial manufacturing activities,
including supplier selection, technology transfer, and ongoing
process optimization for both drug substance and drug product.
- Ensure GMP compliance, robust quality systems, and regulatory
readiness to support commercial supply and global product
launches.
- CMC Strategy and Execution:
- Drive the CMC strategy from late-phase development through
commercialization, collaborating with cross-functional teams
(R&D, Quality, Regulatory, Supply Chain) to ensure seamless
integration of manufacturing processes.
- Lead and advise on CMC-related sections for regulatory
submissions, ensuring alignment with international health authority
expectations.
- Vendor and Partner Management:
- Manage relationships with CDMOs and raw material suppliers,
negotiating contracts, setting performance standards, and
overseeing quality and timelines.
- Continuously evaluate the external network, identifying new
partners and implementing improvements to enhance
cost-effectiveness and supply reliability.
- Team Leadership and Development:
- Build, mentor, and inspire a high-performing team of CMC
professionals, fostering a culture of innovation, accountability,
and continuous improvement.
- Provide strategic guidance on talent development and resource
planning to support evolving business needs.
- Scientific and Technical Expertise:
- Apply broad scientific knowledge of chemistry, process R&D,
and manufacturing best practices to resolve technical
challenges.
- Guide process scale-up, technology transfers, and
troubleshooting activities to ensure product consistency and
on-target performance.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
- Experience: 15+ years in the pharmaceutical industry, with a
focus on small-molecule development, commercial manufacturing, and
CMC leadership. Proven track record in successfully transitioning
products from clinical to commercial scale.
- Technical Expertise: Deep understanding of API and DP
manufacturing, GMP regulations, quality systems, and global supply
chain management.
- Leadership Skills: Demonstrated ability to lead
multidisciplinary teams, manage complex projects, and influence
strategic decision-making in a matrixed environment.
- Regulatory Acumen: Direct experience with global regulatory
filings, inspections, and compliance standards, including authoring
and reviewing Module 3 documentation.
- Education: Advanced degree in Chemistry, Chemical Engineering,
Pharmaceutical Sciences, or a related field preferred.Why Join BBIO
team:You will be part of a team at the forefront of transforming
scientific innovation into commercial reality, playing a pivotal
role in bringing life-changing therapies to patients worldwide. If
you are a strategic leader with a passion for building robust
manufacturing capabilities and elevating global operations, we
encourage you to apply.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.
- 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.
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Keywords: BridgeBio Pharma, Pleasanton , Senior Director, Commercial Manufacturing & CMC Development San Francisco, CA/Hybrid, Executive , Palo Alto, California
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