14 дней назад
Senior Method Development Scientist-Bioanalytical
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Method Development Scientist-Bioanalytical (LC-MS): Performing complex bioanalytical laboratory analyses and supporting method development, validation, and optimization for clinical samples with an accent on quantitative analysis, sample extraction, instrumentation, and data integrity. Focus on troubleshooting non-standard experiments, interpreting complex data, resolving equipment issues, and maintaining GxP-compliant laboratory documentation.
Location: SIMZ Pudong, Shanghai, China
Company
provides laboratory services, diagnostics, data, and technology solutions for healthcare providers, researchers, pharmaceutical companies, and health systems.
What you will do
- Perform complex and non-routine laboratory analyses using established and newly introduced methods and technologies.
- Execute advanced analytical workflows across compounds and biological matrices, including quantitative analysis of clinical samples.
- Support method development, validation, optimization, and the adoption of new laboratory methods, instruments, and platforms.
- Design troubleshooting experiments, perform root cause analysis, resolve technical and equipment-related issues, and recommend solutions.
- Interpret complex data, provide scientifically sound conclusions, and contribute to process, data quality, and laboratory performance improvements.
- Train and mentor junior staff while providing day-to-day technical guidance.
Requirements
- Bachelor’s degree in pharmacy, pharmaceutical analysis, or chemistry.
- At least 3 years of experience in the bioanalytical industry.
- Experience with analytical equipment and troubleshooting.
- Familiarity with standard laboratory equipment and advanced computer applications, including Word and Excel.
- Effective verbal and written communication, presentation, interpersonal, and teamwork skills.
- Ability to maintain accurate, audit-ready documentation and support data integrity, regulatory compliance, and CAPA activities under GxP requirements.
Nice to have
- At least 3 years of experience developing methods for quantitative analysis of clinical samples using LC-MS.
- At least 3 years of hands-on experience with sample extraction using PPT, LLE, and SPE.
Culture & Benefits
- Collaborative, knowledge-sharing laboratory environment.
- Opportunities to contribute to workflow improvement and laboratory capability development.
- Inclusive workplace with equal employment opportunity.
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