Associate Director/Director, Drug Product Manufacturing

bridgebio· Manufacturing
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📍 San Francisco - 1800 Owens

About this role

Mavericks Wanted 

When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on 
  
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. 

What You'll Do

You will be responsible for the oversight of drug product formulation and manufacturing process development and manufacturing at contract manufacturing organizations while facilitating clinical drug product disposition. You will also work with colleagues in CMC, Supply Chain Operations, Quality Assurance, and CMC-regulatory Affairs, while serving as an important point of technical contact between Calcilytix and contract research and manufacturing organizations.

Responsibilities

  • Formulation composition and manufacturing process development (experience with modified/extended release is a plus)
  • Person-in-plant oversight of the clinical and commercial drug product manufacturing process at CMOs (especially for small molecule solid oral dosage forms)
  • Perform activities related to batch review & release, deviations, change controls, investigations and other quality related work
  • Participate & provide input to root-cause analysis and CAPA plans
  • Author/update regulatory filings

Where You'll Work

This is a hybrid role and requires in-office collaboration 2-3x per week in our San Francisco Office. Fully remote could be considered for the right candidate.

Who You Are

  • BS degree in Life Sciences, Engineering, or related field required, advanced degrees preferred
  • · Minimum of twelve (12) years of relevant experience within the pharmaceutical industry required
  • · Solid understanding of CMC manufacturing and analytical activities required in commercial drug product manufacturing, including knowledge of cGMP regulations.
  • · Experience with cGMP quality oversight and on floor production support required
  • · Understanding of Quality Management Systems required
  • · Prior experience as a liaison with solid oral dosage form contract manufacturing organizations required
  • · Experience with polymer characterization (rheology, DSC, TGA), dissolution, extrusion/spraying operations, and enteric coating preferred
  • · Ability to periodically travel (up to 30% at times)

 

#LI-NT1

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
$158,000—$215,000 USD

As a global company, our comprehensive benefits may vary based on location.  We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.

For USA based roles:

Financial & Rewards  

  • 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  

Health & Well-Being  

  • 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  

Skill Development & Career Paths: 

  • 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 

Frequently Asked Questions

Is the salary disclosed for the Associate Director/Director, Drug Product Manufacturing position at bridgebio?
The salary for this Associate Director/Director, Drug Product Manufacturing role at bridgebio is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Associate Director/Director, Drug Product Manufacturing position at bridgebio located?
This Associate Director/Director, Drug Product Manufacturing role at bridgebio is based in San Francisco - 1800 Owens. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Which team or department does the Associate Director/Director, Drug Product Manufacturing at bridgebio belong to?
This Associate Director/Director, Drug Product Manufacturing position is part of the Manufacturing department at bridgebio. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Associate Director/Director, Drug Product Manufacturing position at bridgebio?
Click the "Apply Now" button on this page. You will be redirected to bridgebio's official application portal hosted on greenhouse where you can submit your application directly.
When was the Associate Director/Director, Drug Product Manufacturing job at bridgebio posted?
This Associate Director/Director, Drug Product Manufacturing position at bridgebio was posted on Mar 6, 2026. Apply as soon as possible — early applications are often reviewed first.
Associate Director/Director, Drug Product Manufacturing
bridgebio
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