Job Description
Responsibilities
- Provide process engineering support for the implementation and sustainment of the MES (PAS-X).
- Author, review, and maintain GMP-compliant Standard Operating Procedures (SOPs) and Work Instructions (WIs) related to MES usage, electronic batch records, and process execution.
- Support electronic batch record (eBR) execution, including troubleshooting and continuous improvement activities.
- Ensure alignment of MES functionality with process design, batch execution, and quality systems and compliance requirements.
- Collaborate with cross-functional teams to ensure successful MES integration with manufacturing processes and business systems.
- Contribute to MES-related design review, testing activities and go-live readiness.
- Providing support for the manufacturing of clinical supply drug substance, including resupply activities.
- Contribute to the evaluation, implementation, and qualificati...
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