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Associate Director/Director, CMC, Technical Operations

BridgeBio
Full-time
Remote friendly (Palo Alto, CA)
United States
$160,000 - $245,000 USD yearly
Operations

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Role Summary

Associate Director/Director, CMC, Technical Operations. BridgeBio is seeking an experienced antibody manufacturing and analytical development scientist to expand its biologics-based pipeline, develop analytical methods, and support process and formulation development for antibodies in rare diseases. This role involves collaboration with CRO/CDMO/CMO partners, and requires prior experience with antibodies and CMC analytical requirements for IND/NDA/MAA filings.

Responsibilities

  • Develop analytical methods, and support extended characterization studies for antibody-based therapeutics
  • Support process and formulation development by providing analytical testing results
  • Collaborate with CRO/CDMO/CMO to ensure timely development, validation, testing, and release of materials for clinical activities
  • Author and review protocols, technical reports, and method SOPs
  • Author and review module 3 sections for US and ex-US regulatory filings
  • Manage CRO/CDMO/CMO analytical development activities and timelines
  • Review analytical method transfer documentation and release/stability data for drug substance and drug product
  • Participate in CMC strategic planning and department leadership meetings

Qualifications

  • PhD with 8–10 years or non-PhD with 10–15 years of relevant industry experience
  • Experience with state-of-the-art analytical technologies for biologics (HPLC, CE-SDS, icIEF, LC-MS, peptide/glycan/disulfide maps, DSC, FT-IR, CD, fluorescence, particle analysis)
  • Expertise with current analytical techniques for pharmaceutical development
  • Thorough understanding of cGMPs, USP, ICH guidelines, and industry best practices
  • Experience managing CDMO/CRO from cell line development to IND/FIH
  • Ability to communicate effectively with CRO/CDMO/CMO on project scope, results, and updates
  • Knowledge and experience with CMC analytical requirements for IND and NDA/MAA filings
  • Strong oral and written communication skills
  • Proven leadership and personnel management abilities

Skills

  • Analytical method development and transfer
  • Regulatory filing support (Module 3, US and ex-US)
  • CMC strategy and cross-functional collaboration
  • Project management and CRO/CDMO oversight

Education

  • Doctorate or equivalent experience in a relevant field (e.g., Biochemistry, Analytical Chemistry, Pharmaceutical Sciences)
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