Director, Analytical Development Remote - USA

BridgeBio Inc.; Northern (KY); Hybrid; USD 144,000 - 159,000; Full time

Benefits offered by this job

Market-leading compensation

401(k) with employer match

Employee Stock Purchase Program (ESPP)

Pre-tax commuter benefits (transit and

parking

Referral bonus

Subsidized lunch and parking

Employer-paid medical, dental, and视/v?

Job summary

BridgeBio Inc. is seeking an experienced analytical chemist to lead development and tracking of testing methods for drug substance and product. You will collaborate with internal teams and CRO/CMO partners to advance programs toward regulatory milestones.

The role requires an MS in relevant chemistry fields and 5+ years in pharma/biotech, with expertise in HPLC, cGMP, and analytical method validation. This position offers a remote work model with 30% travel and a strong benefits package.

Qualifications

• MS in Organic Chemistry, Analytical Chemistry, Pharmaceutical Science required.
• 5+ years’ experience in contract research or pharmaceutical/biotech industry.
• Experience with analytical assay development and validation.
• Knowledge of cGMP regulations and USP/EP/JP guidance.

Responsibilities

• Manage the development and tracking of stage-appropriate testing methods for drug substance and drug product.
• Coordinate with internal Analytical, CMC, QA, Regulatory, Project Management and CRO/CMO counterparts.
• Review SOPs, test methods, specifications for materials and products, development/verification reports, validation protocols/reports, method transfers, COAs and stability summaries.
• Support contractor site investigations pertaining to OOS/OOT and deviations.
• Assist in data generation and analysis.
• Ensure analytical development activities are aligned with the project’s objectives.
• Assist in regulatory filings.
• Perform data review & stability tracking.

Skills

Analytical assay development

Impurity analysis

In vitro dissolution release

HPLC

Physicochemical properties

Methods development

Drug substance

Drug product

cGMP regulations

FDA/EMA/ICH guidance

Education

MS in Organic Chemistry, Analytical Chemistry, Pharmaceutical Science

Job description

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 allowsscience and small teams of experts to lead the way. We build bridges to groundbreaking advancements in raredisease, anddevelop 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'llask"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

Responsible for managing the development and tracking of stage-appropriate testing methodology for drug substance and drug product, including in-process, release, stability, method validation and site transfer under aggressive timelines. Communicate and coordinate with internal Analytical, CMC, QA, Regulatory, Project Management and consultants, as well as with external CROs/CMOs counterparts. Manage critical analytical review of SOPs, test methods and specifications for raw materials/intermediates/drug substance/drug product, development/verification reports, validation protocols/reports, method transfers, COAs and stability summaries. Support contractor site investigations pertaining to OOS/OOT and deviations.

Responsibilities

Support Analytical (CMC) activities associated with the formulation of infigratinib.

Work closely with your Analytical Development colleagues and external CROs/CMOs collaborators to rapidly advance programs to key decision points, in preparation of regulatory submission, approval and post-approval commitments.

Assist in data generation and analysis.

Ensure analytical development activities are aligned with the project’s overall objectives.

Assist in regulatory filings.

Perform data review & stability tracking.

Where You'll Work

Remote with 30% travel anticipated

Who You Are

MS in Organic Chemistry, Analytical Chemistry, Pharmaceutical Science.

5+ years’ experience in the contract research or pharmaceutical/biotech industry.

Demonstrated abilities in the development and application of analytical assay, impurity, and in-vitro (dissolution) release.

Experience in high performance liquid chromatography and physicochemical properties (solubility, solid state, physical testing), methods development, drug substance and drug product

Knowledge of cGMP regulations, including compendial (USP, EP, JP) and guidance documents.

Working knowledge of FDA, EMA and ICH guidelines.

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.

$144,000 - $159,000 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 BridgeBio Full-Time U.S Based Roles:

• 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
• HealthSavings 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, continuouseducationand professional development programs via LinkedIn Learning,LifeLabs, &BetterUpCoaching
• We celebratestrong performancewith financial rewards, peer-to-peer recognition, and growth opportunities