Engineer 2 - Process Development (Quality Control)
Контакты
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Singapore
data analysisquality controlbiotechnologyprocess developmentstatistical process controlbiochemistrydesign of experimentslibrary preparation
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Хорошая вакансия
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Чётко описанная роль в разработке процессов у крупной геномной компании предполагает практическую работу на стыке R&D и производства, но офисный формат и отсутствие визового спонсорства ограничивают доступность вакансии.
Без визового спонсорства
Понятные обязанности
Крупная компания в геномике
?Работа на площадке
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Engineer 2 - Process Development (Quality Control) (Biotechnology/Genomics): Developing and improving quality-control processes for high-volume, multi-product manufacturing with an accent on process optimization, biochemical analysis, and production quality. Focus on designing and executing experiments, troubleshooting yield issues, applying DOE and statistical process control, and implementing solutions across R&D, Manufacturing, and Quality.
hirify.global develops genomic technology to support early disease detection, diagnosis, and new treatment options.
What you will do
Support process development, sustaining, definition, improvement, design, development, and quality testing in a high-volume, multi-product manufacturing QC environment.
Establish operating processes, QC specifications, and process improvements.
Troubleshoot QC line issues involving yield and quality, and design and execute experiments to identify solutions.
Conduct process optimization experiments for production release, analyze test results and issue reports, and make technical recommendations.
Collaborate with R&D, Manufacturing, and Quality to develop QC processes for new products and improve processes for existing products.
Define technical requirements and procedures for QC manufacturing processes.
Requirements
Bachelor’s degree in Science or Engineering, or a master’s degree or equivalent in Chemical, Biochemical, Biochemistry, or a bio-related field.
2–5 years of relevant experience in research product development and project management.
Experience with library preparation kits and proficiency in biochemical processes and analysis.
Ability to apply Design of Experiments techniques and Statistical Process Control knowledge.
Ability to analyze data and make logical, rational conclusions.
Excellent organizational skills, attention to detail, documentation skills, and the ability to write procedures and training manuals.
Good inter-departmental communication skills and demonstrated ability to work independently.
Nice to have
Experience in the biotechnology or pharmaceutical industries.
Culture & Benefits
Full-time employment in an inclusive environment focused on collaboration, belonging, and alternative perspectives.
Employee Resource Groups provide career development, cultural awareness, and social responsibility opportunities.
hirify.global is an equal opportunity employer and conducts background checks after conditional offers.
This role is not eligible for visa sponsorship.
Generative AI is prohibited during the application and interview process.
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