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Manufacturing Risk Control (Contract) |
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PURPOSE
- As SME of MES process and also from computerized system point of view
- Ensure implementation and documentation of MES related activities.
- Continuously improve MES as per business needs which include define requirement, apps builder and equipment connectivity, leading User Acceptance Test, and contribute in CSV
- Manage collaboration and alignment with multiple stakeholders regarding MES requirement definition with relevant stakeholders
- Maintain MES related documents, which includes Functional Specification, Configuration Specification, and MES rollout Playbook
SKILLS & REQUIREMENTS
Education
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Bachelor’s degree in Computer Science, Engineering, or Pharmacy
Relevant Experiences
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Minimum 2 years of experience in a manufacturing environment, with at least 1 year in application or IT infrastructure projects
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Experience in leading projects and project management
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Strong knowledge of pharmaceutical manufacturing processes in a GxP-regulated environment
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Experience with Tulip and Inmation platforms will be an advantage
Main Competencies for the Job (Core, Leadership, Technical Competencies)
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Strong analytical thinking
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Self-motivated and driven
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Good communication skills
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Ability to work independently and in a team
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Experience/knowledge in managing multiple stakeholders
Communication
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Fluent in English, both verbal and written
Application Period: | 23/09/2025 | Reference Code: | 853816 | |
Division: | Consumer Health | Location: | Indonesia : West Java : Cimanggis | |
Functional Area: | Production&Manufacturing | Position Grade: | R.11 | |
Employment Type: | Temporary Work | Work Time: | Standard |
Job Segment:
Pharmaceutical, Risk Management, Developer, Java, Computer Science, Science, Finance, Technology