13 дней назад
MES Engineer/Specialist
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
MES Engineer/Specialist (Manufacturing/MES): Implementing, maintaining, optimizing, and managing the lifecycle of a site's Manufacturing Execution System with an accent on system architecture, integrations, validation, and GMP compliance. Focus on integrating IoT devices, troubleshooting complex system issues, supporting regulatory inspections, and improving reliability across manufacturing operations.
Location: Singapore
Company
develops medicines and supports pharmaceutical manufacturing, science, and healthcare innovation globally.
What you will do
- Own the site's Manufacturing Execution System (MES) as Business System Owner and technical subject-matter expert.
- Configure, maintain, upgrade, and optimize MES architecture, databases, Process Instructions, and technical specifications.
- Maintain MES interfaces and connectivity with site systems, including IoT devices and digital solutions.
- Provide advanced troubleshooting and technical support while coordinating with Digital/IT teams and system vendors.
- Lead MES activities for site projects, change controls, deviations, CAPAs, commissioning, and operational handover.
- Monitor performance, downtime, deviations, and recurring issues while driving reliability and user-experience improvements.
Requirements
- Experience supporting or managing a Manufacturing Execution System in a manufacturing environment.
- Ability to work with MES architecture, databases, system integrations, technical specifications, and Process Instructions.
- Knowledge of Computerized System Validation (CSV), GMP, data integrity, cybersecurity, access controls, backup, and recovery processes.
- Ability to prepare SOPs, validation and technical documentation, engineering records, and inspection-support materials.
- Experience collaborating with Manufacturing, Engineering & Maintenance, Digital/IT, Automation, Quality, Validation, global MES teams, and external vendors.
- Ability to work onsite in Singapore.
Culture & Benefits
- Work across manufacturing, engineering, digital, automation, quality, validation, and global MES functions.
- Participate in global MES and digital networks and share lessons learned across initiatives.
- Support operations and end users through technical training and ongoing MES assistance.
- Work in an environment focused on compliant, reliable, and efficient pharmaceutical manufacturing.
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