Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
развернуть
По международному рынку данных пока нет
На СНГ рынке: $1.4к/мес ($1.4к - $2.1к)
78
Хорошая вакансия
развернуть
Чётко очерченная роль в крупной фармкомпании даст узкую экспертизу в регулируемом производстве вакцин и биопрепаратов, но ночные дежурства и экстренная готовность могут влиять на баланс работы и жизни.
Ночные дежурства
Актуальная платформа
Понятные задачи
Производство биопрепаратов
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
MES Engineer/Specialist (OpCenter Pharma): Supporting and improving the OpCenter Pharma MES for production execution and electronic batch record workflows at the Modulus Singapore facility with an accent on system reliability, PI modeling, master data governance, and GxP compliance. Focus on troubleshooting production incidents, leading deviation investigations and CAPA, maintaining validated configurations, and coordinating with Manufacturing, Quality Assurance, Smart Factory, and Digital teams.
Location: Based in Tuas South, Singapore; participation in night-call and after-hours support rotations is required, with possible operational standby for critical system breakdowns.
Company
hirify.global Manufacturing & Supply is developing the Modulus program to create modular, adaptable, multi-product facilities for vaccine and biologics manufacturing.
What you will do
Operate, monitor, maintain, administer, and configure the OpCenter Pharma MES for reliable production execution and electronic batch record workflows.
Provide first-level troubleshooting during night-call and after-hours rotations, prioritize incidents, escalate complex issues, and communicate downtime and major incidents.
Execute PI changes and master data updates while maintaining naming conventions, hierarchies, data governance, and modular, reusable, scalable PI models.
Support and lead MES incident and deviation investigations, including root cause analysis and GMP-aligned CAPA implementation.
Collaborate with Manufacturing, Quality Assurance, Smart Factory, and Digital teams to translate business requirements into MES solutions.
Maintain SOPs, work instructions, design specifications, and other technical documentation for audit readiness.
Requirements
Bachelor’s degree in Engineering, Pharmaceutical, Life Sciences, or a related field, or equivalent experience.
1–10 years of experience supporting or administering an MES in a GMP-regulated pharmaceutical, biotech, or similar manufacturing environment.
Hands-on experience with OpCenter Pharma.
Working knowledge of OpCenter Pharma or similar MES platforms, including configuration and administration.
Experience with master data and PI/process definitions within an MES or similar manufacturing IT system.
Understanding of PI modeling concepts and manufacturing execution in a pharmaceutical setting.
Familiarity with GxP, data integrity, CSV/CSA, and change control principles.
Strong analytical and troubleshooting skills, structured problem-solving, effective communication, teamwork, and sound escalation judgment.
Nice to have
SQL or scripting skills.
Knowledge of MES integration with SCADA, ERP, PLCs, or Smart Factory/IIoT platforms.
Experience with on-call or after-hours production support.
Culture & Benefits
Work within the Modulus program focused on modular, adaptable, and agile facilities for vaccine and biologics manufacturing.
Onsite operational support in Tuas South, Singapore, including night-call and after-hours rotations.
Operational standby may be required for critical MES system breakdowns.
Equal-opportunity environment welcoming people from different backgrounds and locations.
Будьте осторожны
Если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого. Это мошенники. Обязательно жмите «Пожаловаться» или пишите в поддержку. Подробнее в гайде →