Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Хорошая вакансия
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В Company hidden хорошо описана старшая производственная роль в сфере клеточной и генной терапии, а условия развития выглядят привлекательно, но смены по 12 часов могут заметно влиять на баланс работы и личной жизни.
Длинные смены
Понятные обязанности
Клеточная терапия
Развитие и обучение
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Biotechnologist, MFG (CGT) (Biotechnology): Executing cGMP manufacturing for cell and gene therapy treatments with an accent on aseptic processing, cleanroom operations, data integrity, and quality systems. Focus on troubleshooting critical process parameters, leading deviation investigations and CAPAs, driving process improvements, and coaching junior team members.
Location: Tuas, Singapore; onsite cleanroom manufacturing with a rotating 12-hour shift pattern
Company
hirify.global manufactures medicines and therapies across a globally connected network of more than 30 sites on five continents.
What you will do
Execute cGMP manufacturing activities using aseptic techniques, cleanroom practices, and approved procedures.
Complete and review batch records, logbooks, and GMP documentation while maintaining data integrity.
Perform environmental monitoring, equipment preparation, cleaning, and routine production support.
Monitor critical process parameters, troubleshoot equipment and process issues, and escalate non-routine events.
Support deviation investigations, CAPAs, change controls, and work notifications through DMS, LIMS, and TrackWise.
Coach junior team members, maintain training compliance, and drive continuous improvement and assigned operational responsibilities.
Requirements
Degree or equivalent qualification or experience in Biotechnology, Biochemistry, Life Sciences, Engineering, or a related discipline.
Hands-on experience in biopharmaceutical manufacturing or a comparable GMP-regulated manufacturing environment.
Strong technical knowledge of biopharmaceutical processing, aseptic techniques, and cleanroom operations.
Understanding of cGMP, critical process parameters, quality systems, and data integrity requirements.
Experience with process or equipment troubleshooting, deviation investigations, CAPAs, and change controls.
Strong communication, problem-solving, and teamwork skills, including the ability to coach and guide colleagues.
Ability to work in a cleanroom manufacturing environment and perform a rotating 12-hour shift pattern.
Culture & Benefits
Agile career development, ongoing learning opportunities, and a dynamic, inclusive, and ethical workplace.
Performance-based compensation programs and shift allowances.
Fully paid medical insurance, with family coverage available at partially subsidized premiums.
Daily company bus services from designated MRT locations to and from the Tuas site.
Global benefits and a culture focused on collaboration, accountability, excellence, passion, integrity, and diversity.
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