Manufacturing Risk Control (Contract)
PURPOSE
This position is responsible for supporting GMP compliance and digital operational excellence in the Manufacturing Business Unit by executing core manufacturing operations and documentation activities
The key roles is to drive value realization from Manufacturing Execution System with risk-based approach, to ensure consistent and rigorous application across end-to-end process
MAJOR TASKS
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
Bachelor’s degree in Computer Science, Engineering, or Pharmacy
Relevant Experiences
Minimum 2 years of experience in a manufacturing environment, with at least 1 year in application or IT infrastructure projects
Experience in leading projects and project management
Strong knowledge of pharmaceutical manufacturing processes in a GxP-regulated environment
Experience with Tulip and Inmation platforms will be an advantage
Main Competencies for the Job (Core, Leadership, Technical Competencies)
Strong analytical thinking
Self-motivated and driven
Good communication skills
Ability to work independently and in a team
Experience/knowledge in managing multiple stakeholders
Communication
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