
Pharmaceutical MES Technical Expert
1 day ago
The Site SME MES Project is a key functional and technical expert responsible for supporting the successful implementation of the Manufacturing Execution System (MES) & L2 at multiple pharmaceutical manufacturing sites.
This role ensures that site-specific manufacturing processes are accurately captured and reflected in the global MES solution. The SME is accountable for leading site-level validation activities, technical owner responsibility, and managing all GxP documentation related to the MES & L2 system.
Key Responsibilities:
- Lead site-level validation activities to ensure compliance with regulatory requirements
- Manage all GxP documentation related to the MES & L2 system
- Provide technical expertise on system functionality, configuration, and compliance requirements
Requirements:
- 6-8 years of experience in the pharmaceutical industry, including technical and functional experience in MES & L2 systems
- Deep understanding of system functionality, configuration, and compliance requirements
- Excellent communication and problem-solving skills
Benefits:
- Opportunity to work with a leading pharmaceutical company
- Competitive compensation and benefits package
- Chance to develop skills and expertise in MES & L2 systems
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