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Remote Director Analytical Development Jobs (NOW HIRING)

BridgeBio Pharma

Director, Analytical Development

Work closely with your Analytical Development colleagues and external CROs/CMOs collaborators to ... Where You'll Work Remote with 30% travel anticipated Who You Are MS in Organic Chemistry ...

BridgeBio Pharma

Director, Analytical Development

$144K - $159K/yr

Work closely with your Analytical Development colleagues and external CROs/CMOs collaborators to ... Where You'll Work Remote with 30% travel anticipated Who You Are MS in Organic Chemistry ...

Iambic Therapeutics, Inc

$224K - $310K/yr

JOB SUMMARY Iambic Therapeutics is seeking a Senior or Executive Director to lead the analytical development and QC function within CMC. This leadership role will provide scientific, strategic, and ...

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How much do remote director analytical development jobs pay per year?

As of Sep 15, 2026, the average yearly pay for remote director analytical development in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.
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Infographic showing various Remote Director Analytical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $191,412 per year, or $92 per hour.

Director, Analytical Development

Remote

BridgeBio Pharma
Biotechnology Research and Development • 201 - 500 employees
Learn more about BridgeBio Pharmaexternal

Full-time

Re-posted 11 days ago

Job description

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.

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