Senior Scientist, Analytical Sciences (Contract)

• Independently lead analytical development and product characterization activities for one or more molecules in CMC development.
• Able to independently develop and optimize analytical methods to support early and late-stage development. Expected to solve challenging problems by application of one or more (traditional or emerging) analytical techniques.
• Independently design experiments perform sample analysis using general laboratory techniques such as weighing pipetting and operating laboratory instruments (HPLC LC-MS GC UV-Vis KF DSC TGA XRPD etc.).
• Execute analysis with a solid understanding of the test procedures underlying science and proper instrument operation ensuring accurate and reliable results.
• Utilize available software to control instruments collect data process and calculate results and prepare comprehensive reports.
• Maintain precise and comprehensive records of all analyses in a lab notebook in real time ensuring compliance with company standards and promoting traceability and consistency in data reporting.
• Prepare presentation materials and clearly communicate research results to the manager and present at internal meetings.
• Author/review technical reports technical packages and relevant sections in health authority filings.

Qualifications :

• Requires a . degree in chemistry with >8 years of relevant research experience or a Ph.D. degree with a minimum of 3 years of hands-on pharmaceutical/biotech industry experience or equivalent in the field of new drug discovery and development.
• Hands-on experience with laboratory techniques including chromatography (e.g. HPLC GC LC/MS) spectroscopy (e.g. UV-Vis FTIR) titration methods (e.g. Karl Fischer acid-base) dissolution testing particle size analysis (by laser diffraction) microscopy and other compendial methods.
• Experience using laboratory software to collect analyze and report data. This might include instrument control software (Openlab Empower etc.) or data analysis programs (Excel etc.).
• A strong attention to detail and demonstrated prior experience working in GLP cGMP environment.
• Demonstrated ability to take initiative ownership problem identification problem solving and strategic input.
• Excellent communication and organization skills; ability to work independently and efficiently collaborate in a fast-paced integrated multidisciplinary team environment.
• Exceptional problem-solving skills scientific curiosity critical thinking and ability to quickly adapt and shift focus as needed.
• Experience working in late-stage development or commercialization environments is preferred.
• Hands-on in-plant experience within a manufacturing or production setting is highly preferred.

Additional Information :

The anticipated base salary for candidates who will work on-site at our South San Francisco location is between $75.00-$85.00/ per hour 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.

ORIC Pharmaceuticals Inc. is an equal opportunity employer. ORIC does not discriminate based on race color religion gender sexual orientation gender identity age national origin disability status protected veteran status or any other legally protected characteristics.

Remote Work :

No

Employment Type :

Contract