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Home›Jobs›BridgeBio›Sr. Scientist/Associate Director, Drug Substance, Development & Manufacturing
BridgeBio

About BridgeBio

Bridging science and hope for genetic diseases

🏢 Tech, Biotechnology👥 251-1K📅 Founded 2014📍 Palo Alto, California, United States

Key Highlights

  • Public company (NASDAQ: BBIO) with strong market presence
  • Over 15 drug development programs targeting rare genetic diseases
  • $1.5B+ raised from top investors like OrbiMed
  • Headquartered in Palo Alto, California

BridgeBio (NASDAQ: BBIO) is a biopharmaceutical company headquartered in Palo Alto, California, focused on developing innovative medicines for genetic diseases. With a pipeline of over 15 programs, BridgeBio aims to address unmet medical needs for rare genetic conditions, leveraging advancements in ...

🎁 Benefits

BridgeBio offers competitive salaries, equity options, comprehensive health benefits, and generous PTO policies. Employees also enjoy a flexible work ...

🌟 Culture

BridgeBio fosters a culture of innovation and collaboration, emphasizing the importance of scientific rigor and entrepreneurial spirit. The company va...

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BridgeBio

Sr. Scientist/Associate Director, Drug Substance, Development & Manufacturing

BridgeBio • San Francisco, CA/Hybrid

Posted 2d ago🏢 HybridSeniorResearch scientist📍 San francisco
Apply Now →

Overview

BridgeBio is seeking a Senior Scientist/Associate Director for Drug Substance Development and Manufacturing. You'll support the development of life-changing medicines for patients with unmet needs. This role requires extensive experience in drug development and manufacturing processes.

Job Description

Who you are

You have a strong background in drug substance development and manufacturing, with a proven track record of leading projects in the biopharmaceutical industry. Your expertise includes understanding the complexities of drug formulation and the regulatory landscape surrounding drug development. You thrive in collaborative environments and are passionate about pushing the boundaries of science to deliver innovative solutions for patients.

You possess excellent problem-solving skills and can navigate challenges with creativity and resilience. Your experience in managing cross-functional teams has equipped you with the ability to communicate effectively with various stakeholders, ensuring that projects stay on track and meet their objectives. You are driven by a desire to make a meaningful impact in the field of rare diseases and are excited about the opportunity to work with some of the most respected minds in the industry.

Desirable

Experience with clinical development processes and regulatory submissions is a plus. Familiarity with orphan drug designation and fast track designation processes will enhance your ability to contribute to our mission. A background in working with small teams and a willingness to embrace unconventional approaches to problem-solving will set you apart.

What you'll do

As a Senior Scientist/Associate Director, you will play a pivotal role in the development and manufacturing of drug substances. You will lead efforts to optimize processes, ensuring that they are efficient and compliant with regulatory standards. Your responsibilities will include overseeing the formulation development, scale-up processes, and the transfer of technology to manufacturing sites.

You will collaborate closely with cross-functional teams, including research, quality assurance, and regulatory affairs, to ensure that all aspects of drug development are aligned. Your insights will guide the strategic direction of projects, and you will be responsible for presenting findings to senior leadership and external stakeholders.

In this role, you will also mentor junior scientists, fostering a culture of innovation and continuous improvement within the team. You will be expected to stay abreast of industry trends and advancements, integrating new knowledge into your work to enhance our capabilities.

What we offer

At BridgeBio, we offer a dynamic and supportive work environment where innovation is encouraged. You will have the opportunity to work on groundbreaking projects that have the potential to change lives. We provide competitive compensation, including a salary range of $160,000 to $215,000 USD, and a comprehensive benefits package designed to support your well-being and professional growth.

Join us in our mission to redefine the future of biopharma and make a lasting impact on patients with unmet needs. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse perspectives and backgrounds.

Interested in this role?

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