3 часа назад
Research Associate II / Senior Research Associate / Scientist, Analytical Development & Quality Control
72 384 - 133 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Research Associate II / Senior Research Associate / Scientist, Analytical Development & Quality Control (Analytical Chemistry): Executing release and stability testing for drug substance intermediates, drug substances, and drug products with an accent on LC-MS, HPLC, GC, GMP, and analytical method validation. Focus on managing external laboratory activities, investigating analytical results, optimizing methods, and preparing scientific and regulatory reports.
Location: Onsite in Carlsbad, California, United States
Salary: $72,384–$133,000 annually, depending on level. Research Associate II: $72,384–$89,730; Senior Research Associate: $84,257–$108,647; Scientist: $97,774–$133,000.
Company
is a biotechnology company developing RNA-targeted medicines and gene-editing approaches for serious diseases, with programs in neurology, cardiology, and other high-need areas.
What you will do
- Execute release and stability testing for drug substance intermediates, drug substances, and drug products.
- Manage outsourced analytical activities at external contract laboratories.
- Review analytical data for compliance with analytical methods, equipment procedures, material specifications, and SOPs.
- Conduct analytical investigations and solve technical problems.
- Develop or optimize analytical methods and execute method validation and transfer protocols.
- Author scientific reports, contribute to CMC regulatory filings, and present findings at internal and cross-functional meetings.
Requirements
- BS or MS in Analytical Chemistry or a related discipline with at least 2 years of industry experience for Research Associate II or 5 years for Senior Research Associate; PhD candidates may be considered for the Scientist level.
- Practical experience operating LC-MS, HPLC, and GC instrumentation.
- Understanding of the drug development process, GMP requirements, and ICH and FDA method validation guidelines.
- Ability to manage priorities, solve problems, and maintain aggressive timelines across multiple projects.
- Ability to work independently and productively within a team or matrix environment.
- Excellent written and verbal communication skills.
Culture & Benefits
- Onsite work environment focused on scientific excellence, innovation, and collaboration.
- Opportunities to contribute to medicines for patients with serious diseases and unmet needs.
- Benefits package available to employees.
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