api testinggmpanalytical chemistrymethod validationcgmphplcuplchplc ms
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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У вакансии понятные исследовательские задачи, релевантные требования по аналитической химии и четкие границы роли в известной компании научного приборостроения.
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Сильный работодатель
?Узкая специализация
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Текст:
Hirify AI/Оригинал
TL;DR
Research Associate, Analytical Chemitry (Analytical Chemistry/API Manufacturing): Executing analytical techniques and laboratory-scale experiments to support method validation for active pharmaceutical ingredient manufacturing with an accent on HPLC/UPLC, mass spectrometry, and cGMP compliance. Focus on authoring validation protocols and reports, troubleshooting laboratory instrumentation, and presenting research summaries to interdisciplinary teams.
Location: US-CO-Frederick, United States
Salary: $85,840.00–$134,125.00 per year, plus eligibility for bonus, stock, and benefits.
Company
hirify.global develops analytical instruments and solutions supporting pharmaceutical and other research applications.
What you will do
Design and conduct laboratory-scale experiments supporting analytical method validation for active pharmaceutical ingredient manufacturing.
Execute analytical methods using HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, and Karl Fischer platforms.
Author method validation protocols and reports in accordance with ICH guidelines and internal SOPs.
Record, summarize, and present experimental results through laboratory notebooks, reports, and research summaries.
Maintain compliance with SOPs and current good manufacturing practices while operating, troubleshooting, and maintaining laboratory equipment.
Requirements
Bachelor’s degree or equivalent in chemistry or a related applied science field.
At least 4 years of relevant experience.
Experience following SOPs for analytical method execution, including HPLC/UPLC and HPLC-MS.
Nice to have
Experience with IC, GC, GC-MS, UV, and Karl Fischer.
Experience in a cGMP-regulated environment.
Knowledge of analytical test methods for oligonucleotide APIs or related molecules.
Experience with method validation.
Ability to work with interdisciplinary project teams, understand project requirements, and follow project timelines.
Culture & Benefits
Full-time daytime schedule with no stated end date.
Bonus, stock, and benefits may be available.
No travel is required.
Inclusive, equal-opportunity workplace with accessibility support available during the application and interview process.
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