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Director, Analytical Chemistry

Scribe Therapeutics

Scribe Therapeutics

Administration
Alameda, CA, USA
Posted on Friday, December 16, 2022

Scribe Therapeutics is a molecular engineering company focused on creating best-in-class in vivo therapies that permanently treat the underlying cause of disease. Founded by CRISPR inventors and leading molecular engineers Benjamin Oakes, Brett Staahl, David Savage, and Jennifer Doudna, Scribe is overcoming the limitations of current genome editing technologies by developing custom engineered enzymes and delivery modalities as part of a proprietary, evergreen CRISPR by Design™ platform for CRISPR-based genetic medicine.

We are seeking a highly creative, passionate, and motivated individual to join us in our quest to develop the next generation of CRISPR-based therapeutics. The current role is for a Director of Analytical Chemistry to join the Technical Operation’s leadership team and advance Scribe’s platform. The candidate should have a passion for working collaboratively to enable building the necessary analytical tools, methods, and strategy to meet the new frontier of CRISPR-based therapeutics. Additionally, the candidate would bring expertise in phase-appropriate analytical CMC strategy for drug substance and drug product, knowledge of state-of-the-art analytical technologies for AAV and LNP.

The candidate will have the opportunity to build their team in a rapidly growing biotechnology start-up and the ability to be involved in bringing the next generation gene editing drug products to the patients.

Key Responsibilities:

  • Building and leading a team of research specialists and scientists in the Analytical Chemistry Group to design and implement the analytical chemistry methods (biological and physiochemical) and characterization strategies to identify and justify critical quality attributes (CQAs) for Scribe’s critical starting materials, drug substance, and drug product
  • Develop phase-appropriate quality control strategy for drug substance and drug product
  • Advanced knowledge and hands-on experience in areas including but not limited to HPLC, CE or LC-MS or ELISA, MSD and ddPCR based techniques to guide process development, process understanding, product characterization, stability, and release testing (Find opportunities for improvement and/or new technology development in drug development-related analytics for implementation)
  • Partnering with process teams to develop the residual clearance strategies for genetic therapies and support the process related residuals methods development
  • Advance scientific understanding of critical reagents, nanoparticle, viral vector based drug products, CQAs and correlation to product efficacy and safety
  • Author and review relevant sections of CMC documentation in support of INDs, CTAs, BLA submissions, amendments, and briefing documents
  • Work with Research, PRe-clinical, Process Science, Quality and Regulatory groups to set appropriate product specifications, develop comparability strategies and support manufacturing investigations.
  • Establish regular interface and build strong connections with CDMOs and contract labs
  • Formulate and implement successful CMC and regulatory strategies for drug substance and drug products and pipeline that are fit for purpose, phase-appropriate, and position programs well for approval.
  • Strong understanding of global CMC regulatory requirements and industry guidance and provide direction on the interpretation and application of regulations/guidance for gene editing platforms
  • Ensure CMC regulatory strategy is aligned with the Scribe’s global development strategy, therapeutic area portfolio, commercial plans, the Target Product Profile (TPP), and Quality target product profile (QTPP)
  • Assist in negotiations with regulatory agencies to resolve CMC issues and foster positive interactions with regulators, eg, pre-IND, end-of-phase, scientific advice meetings, information requests, clinical holds
  • Lead, plan, author, and review CMC submission documents, including agency meeting packages such as Module 3 and Module 2.3 for clinical and marketing applications, supplements, variations, and responses to agency information requests
  • Interface with Quality, CMOs, and other strategic partners * Identify risks and diplomatically propose risk mitigation strategies
  • Build, guide, and invest in the development of a team of direct reports, creating a safe space where they can come as they are and apply their talents to meaningful and satisfying work
  • Review and provide feedback on the work of colleagues, contribute personal expertise to the broader team and be open to learning/cross-training in other areas, lead and develop other team members as needed per our matrix team business model

Required Skills and Background:

  • Ph.D. in Bio-Analytical Chemistry, Molecular Biology, or other related disciplines and 8 years of experience in gene therapy or gene editing products.
  • Significant experience in developing analytical chemistry-based methods for characterization of critical reagents, nanoparticle and viral vectors drug products and process related residuals to advance product understanding, process development and the establishment of control strategies
  • Problem solver with the ability to leverage novel analytical technologies to deeply and broadly advancing Scribe’s knowledge of physicochemical and biological properties to support product and process development
  • Experience with critical reagents, raw materials physicochemical properties, functional assays and purity/impurities assays
  • Working knowledge and interpretation of FDA/EMA and ICH regulations and guidelines
  • Demonstrated technical proficiency, scientific creativity, collaboration with department and with drug development groups.
  • Strong verbal and written communication skills. Ability to communicate effectively with others internally and externally to the organization
  • Strive for scientific excellence and focus on delivering results
  • People leader

Preferred Skills and Background:

  • Familiarity with CRISPR technologies and therapeutic approaches
  • Familiarity with protein or RNA structure and engineering approaches

Salary will be commensurate with experience. We will provide an intellectually stimulating, collegial and fast-paced environment. If you are ready to engineer the future of therapeutics, then we are excited to hear from you! Visit us at www.scribetx.com.

We are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, age, or veteran status.