About ORIC Pharmaceuticals
ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives by Overcoming Resistance In Cancer. Backed by Correlation Ventures.
About the role
The anticipated base salary for candidates who will work on-site at our San Diego location is between $170,000-$185,000 per year. The final rate offered to a successful candidate will be dependent on several factors that may include, title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors. This position is not eligible for H-1B visa sponsorship. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- Ph.D. in analytical chemistry or relevant field with 7-10+ years of relevant hands-on pharmaceutical/biotech industry experience, or equivalent, in the field of new drug discovery and development
- Demonstrated problem-solving skills, scientific curiosity, passion, critical thinking, and ability to quickly adapt and shift focus as needed
- Demonstrated ability to take initiative, ownership, problem identification, problem solving and strategic input. A proven record of sustained laboratory achievement and innovation
- Proven track record of Person-in-Plant (PIP) oversight and a history of working within a late-stage commercial company are highly preferred
- Awareness and knowledge of cross-functional activities such as toxicology and clinical development
- Experience in writing and reviewing product specifications, method validation protocol/ reports, analytical methods, development reports, risk assessments, release, and stability
More about this role
- Management of outsourced and in-house research activities. Function as a subject matter expert for tech transfer/development of processes to external vendors (contract development and manufacturing organizations/contract testing organizations, CDMOs/CTOs). 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 stakeholders and customers across all stages of drug development, from clinical to commercial.
- Independently lead and oversee analytical method development, validation, solid state characterization, release/ stability testing, data review and trending, retest/shelf-life extensions and NDA enabling activities at CDMOs and in-house.
- Manage GMP manufacturing and product characterization activities at external partners, including preparation and review of analytical methods, Method Validation Protocols, Method Validation Reports, Stability protocols, and CoAs; work closely with process colleagues to propose/ justify specifications for RSMs, IPCs, intermediates, and API based upon batch history...
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