problem solvingdata integrityquality systemsgxplaboratory operationscgmpmammalian cell culturebiopharmaceutical manufacturing
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Структурированная 15-месячная программа у крупного производителя биопрепаратов даёт понятный вход в разработку клеточных процессов, но зарплата не указана, а работа полностью на площадке ограничивает гибкость.
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Зарплата не указанаОбучение с практикойКрупный работодатель
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
AnT1 Trainee, Development Services (Biopharma): Developing cell culture processes that enable the manufacture of recombinant protein therapeutics with an accent on mammalian cell culture, cGMP documentation, and GxP compliance. Focus on performing laboratory work, maintaining data integrity, troubleshooting equipment, and improving operational efficiency at a fully site-based facility.
Location: SG - Tuas, Singapore. Fully site-based at Science Park Facility.
Company
hirify.global manufactures medicines and supports the development of customers’ breakthrough ideas into viable therapies through globally connected teams across more than 30 sites.
What you will do
Develop cell culture processes that enable the manufacture of recombinant protein therapeutics.
Perform mammalian cell culture activities with support from the Manager or Study Lead.
Plan and prioritize laboratory work, draft laboratory records, and document results according to hirify.global policies and current Good Manufacturing Practices.
Follow EHS, Quality, GxP, regulatory, and data integrity requirements, and proactively identify improvements to data integrity processes.
Provide general laboratory support, including housekeeping, equipment maintenance, and inventory management.
Troubleshoot equipment issues and contribute to operational efficiency.
Requirements
Degree in a relevant Science field or equivalent.
Understanding of mammalian cell culture applications for biopharmaceutical production.
Understanding of cGMP regulations.
Good problem-solving and analytical skills.
Good communication and teamwork skills.
Adherence to EHS rules, Quality and GxP requirements, applicable regulatory standards, and data integrity principles.
Culture & Benefits
15-month Career Conversion Program training period.
Structured on-the-job training is provided at the participating company.
In-person collaboration supports real-time teamwork and the technical precision required for medicine manufacturing.
Work within a culture based on Collaboration, Accountability, Excellence, Passion, and Integrity.
Inclusive environment that values diverse perspectives and employee ideas.
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