Associate Director, Process Chemistry

ORIC Pharmaceuticals•South San Francisco, CA

3d•$175,000 - $200,000

About The Position

ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives by Overcoming Resistance In Cancer. ORIC’s clinical stage product candidates include (1) ORIC-944, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) ORIC-114, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. We are seeking a highly motivated process development and chemistry Associate Director with a proven record of sustained laboratory achievement and innovation to join our growing Pharmaceutical Sciences (Pharm Sci) group at ORIC Pharmaceuticals, responsible for Chemistry, Manufacturing, and Controls (CMC). The successful candidate will report to the Senior Director of Process Chemistry and will be responsible for the following.

Requirements

PhD in organic chemistry with 10+years of relevant hands-on pharmaceutical/biotech industry experience, or equivalent, in the field of new drug discovery and development
Proven track record for solving process chemistry problems, including identification, optimization, and characterization of robust and scalable synthetic routes.
Scientific excellence as demonstrated by publications, presentations, and leadership/engagement in the scientific/professional community.
Working understanding of analytical tools used in process development (DSC, TGA, DVS, HPLC, NMR, KF, PLM, XRPD).
Understanding of reaction safety hazards assessment and its application to reaction scale-up.
Detailed understanding of process characterization in preparation for validation, including experience with using statistical methods for reaction modeling to support filings.
Experience in tech transfer, scale-up, manufacturing on multikilogram scale, and working in GMP environment.
Demonstrated ability to work independently and efficiently in a collaborative, fast-paced, integrated, multidisciplinary team environment that includes work internally and with external partners, such as research organizations/Universities, CROs, CMOs, and CDMOs.
Experience in writing and reviewing batch records, specifications, stability protocols/data review, and development reports.
Demonstrated ability to quickly adapt and find creative solutions to ensure deliverables are met, as external environment and stakeholder input evolves.
Excellent oral and written communication skills.
Succinct but thorough communication skills with attention to detail, analytical/critical thinking, and data organization, presentation, and inference.

Nice To Haves

Experience in late-stage pharmaceutical and process chemistry drug development, including putting together data and documents towards, authoring/reviewing, and submitting an NDA for a small molecule commercial product highly preferred.

Responsibilities

Management of outsourced and in-house research and development activities.
Lead drug substance activities on one or more projects.
Function as a subject matter expert for transfer/development of processes to external vendors and CMOs.
Create and execute plans for external projects by providing technical guidance, strategic and tactical direction, and oversight to ensure the product requirements are designed and delivered appropriately and in a timely manner for all the stakeholders and customers, across all the stages of drug development - from discovery through preclinical to clinical and commercial.
Management of GMP manufacturing activities at external partners including preparation and review of MBRs and EBRs, work closely with Analytical Sciences to support method development and validation, and manage quality event resolution for GMP compliance.
Lead scientific and technical thinking on assigned projects.
Effectively working cross-functionally with Regulatory, Quality, Analytical and Formulations Development colleagues to deliver on program objectives and deliverables.
Author and review technical reports, technical packages, relevant sections in health authority filings (including INDs, NDAs, annual reports, and any other regulatory interactions), and contribute to regulatory filing strategy.
Prepare presentation materials and clearly communicate research results to manager, and at internal/external meetings.
Work closely with clinical and preclinical colleagues for need forecasting and supply logistics, including CMO selection, enablement and troubleshooting at site, and tech transfer.
Proactively coordinate and work with CROs, CDMOs, and CMOs ensuring uninterrupted clinical supplies.
Communication excellence in project management; budget planning, oversight in partnership with quality, regulatory, clinical and preclinical departments.
Periodic documentation of progress and accruals, and contract/PO/invoice coordination with finance.