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Senior Researcher
Job in
San Diego, San Diego County, California, 92189, USA
Listed on 2026-01-27
Listing for:
BioPhase
Full Time
position Listed on 2026-01-27
Job specializations:
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Research Scientist, Clinical Research, Medical Science
Job Description & How to Apply Below
Seeking an experienced analytical chemist to join our Analytical Development & Quality Control (ADQC) group at the Sr. Research Associate, Senior Scientist or Assistant Director level (depending on experience). The ideal candidate will be familiar with a broad range of analytical chemistry techniques, possess a strong work ethic and strong technical background, demonstrate excellent oral and written communication skills, and have experience working in a GMP environment.
The successful candidate will be able to perform the following responsibilities with a high degree of independence and attention to detail.
- Manage the analytical activities for oligonucleotide therapeutic development projects
- Coordinate and execute testing of drug substance intermediate, drug substance, and drug product samples for release and stability studies
- Manage outsourced analytical activities at external contract labs
- Conduct analytical investigations
- Develop and optimize analytical methods
- Develop drug substance specifications ensuring efficient integration across Chemistry, Manufacturing, and Controls (CMC) and other relevant disciplines such as Clinical and Toxicology
- Design and execute method validation and method transfer protocols
- Author scientific reports and portions of the CMC section of regulatory filings
- Present at internal and cross-functional scientific meetings
- BS or MS with at least 5 years (Sr. Research Associate) or 10 years (Assistant Director) of industry experience in Analytical Chemistry or related discipline
- Ph.D. with at least 2 years (Sr. Scientist) or 7 years (Assistant Director) of industry experience in Analytical Chemistry or a related discipline
- Skilled in operating LC-MS, HPLC, and GC for the analysis of drug substance and drug product samples
- Good understanding of the drug development process
- Practical knowledge of GMP requirements, with hands-on GMP experience preferred
- Good understanding of ICH and FDA method validation guidelines, including phase-appropriate strategies
- Ability to problem solve, manage priorities and maintain aggressive timelines for multiple projects
- Ability to work productively and independently within a team or matrix environment
- Excellent written and verbal communication skills
Position Requirements
10+ Years
work experience
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