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Associate Director/Director, Analytical Development - Brisbane California
Company: Mammoth Biosciences Location: Brisbane, California
Posted On: 05/08/2025
Mammoth BioSciencesOPPORTUNITYMammoth seeks an Associate Director/Director, Analytical Development to lead and oversee all analytical development activities to support the development, characterization, and commercialization of pharmaceutical products. This includes managing method development and validation, supporting process development, ensuring product quality, and guiding regulatory strategy related to analytical controls. The individual will play a key role in setting analytical strategy, mentoring staff, managing external partnerships, and ensuring compliance with regulatory expectations. KEY RESPONSIBILITIES - Leadership & Strategy:
- Provide scientific and strategic leadership for analytical development across all stages of drug development
- Collaborate cross-functionally with Process Development, Formulation, Quality, Regulatory Affairs, and external partners
- Method Development & Validation:
- Oversee the development, optimization, qualification, and validation of analytical methods (e.g., HPLC, GC, LC-MS, CE, spectroscopy, cell based)
- Guide strategies for analytical control strategies including specifications and stability-indicating methods
- Product & Process Support:
- Support raw material, in-process, drug substance, and drug product testing
- Lead analytical support for process development, formulation, comparability studies, and technology transfer
- Regulatory & Compliance:
- Author, review, and approve analytical sections of regulatory filings (INDs, IMPDs, BLAs/NDAs)
- Ensure compliance with ICH, FDA, EMA, and other global regulatory guidelines
- Support audits, inspections, and quality investigations as needed
- Outsourcing & Vendor Management:
- Oversee outsourced analytical activities at CROs and CDMOs
- Manage technical transfer of methods and ensure timely and high-quality data deliveryREQUIRED QUALIFICATIONS
- Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or related discipline, with a minimum of 6 years of relevant industry experience (or equivalent combination of education and experience)
- Demonstrated expertise in analytical method development, validation, and regulatory filings
- Experience with both small molecule and/or biologics analytical techniques
- Strong understanding of GMP, ICH guidelines, and regulatory expectations
- Proven leadership and management experience, including mentoring scientific staff
- Excellent written and verbal communication skills
- Ability to work onsite or commute to our Brisbane, CA location regularly
- Ability to work Pacific Time Zone if not located within the west coastPREFERRED QUALIFICATIONS
- Experience with Gene editing modalities is highly preferred
- Experience supporting early stage projects
- Familiarity with QbD principles and lifecycle management of analytical methods
- Direct experience with managing CDMOs and CROsBENEFITS
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