QC System Administrator Trainee (Career Conversion Program)
Контакты
Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
Singapore
digital solutionsmaster dataqualificationgxpcapabiopharmaceuticalsqc systems
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
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$34к$44кмедиана$58к
48 в выборке
85
Крутая вакансия
развернуть
Структурированный вход в фарминдустрию в глобальном гиганте с четким путем развития через программу переподготовки.
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Зарплата не указанаСовременные стандартыСильный доменКарьерный лифтПонятный скоуп
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
QC System Administrator Trainee (Career Conversion Program) (QC digital solutions and GxP qualification): Supporting the deployment, maintenance, validation, and user administration of QC laboratory systems in a biopharmaceutical manufacturing environment with an accent on documentation, equipment qualification, and regulatory compliance. Focus on maintaining master data and access, supporting CAPA investigations, and optimizing laboratory processes.
Location: City of Singapore
Company
hirify.global is a global healthcare company developing and delivering medicines and vaccines. The hirify.global Modulus initiative focuses on evolutive, multi-product manufacturing facilities that use disruptive technologies to address biologics manufacturing challenges.
What you will do
Support local deployments of QC digital solutions according to deployment plans and validation protocols.
Issue and maintain local documentation required for the appropriate use and maintenance of QC digital solutions.
Provide training and end-user support for QC digital tools.
Maintain master data and end-user access in accordance with defined requirements and documentation.
Support qualification of QC equipment by preparing protocols, risk assessments, and reports, and contribute to GxP asset qualification compliance.
Report digital-system events, participate in investigations, execute assigned CAPA activities, and contribute to QC laboratory process improvements.
Requirements
Diploma or degree in Pharmaceutical Sciences, Applied Science, or a related life sciences discipline.
Self-starter and independent worker able to operate effectively in cross-functional teams.
Strong analytical and critical-thinking skills, with the ability to solve problems and navigate complexity and ambiguity.
Ability to work in fast-paced, dynamic conditions with tight timelines.
Nice to have
Prior internships or industrial attachments in biopharmaceutical or biotechnology organizations.
Culture & Benefits
Work in a global healthcare environment focused on medicines, vaccines, science, and manufacturing innovation.
Collaborate with people from different backgrounds, locations, and functional areas.
Equal-opportunity employment regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability, or gender identity.
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